Abstract
The SORL1 gene has recently emerged as a strong Alzheimer’s Disease (AD) risk gene. Over 500 different variants have been identified in the gene and the contribution of individual variants to AD development and progression is still largely unknown. Here, we describe a family consisting of 2 parents and 5 offspring. Both parents were affected with dementia and one had confirmed AD pathology with an age of onset > 75 years. All offspring were affected with AD with ages at onset ranging from 53 years to 74 years. DNA was available from the parent with confirmed AD and 5 offspring. We identified a coding variant, p.(Arg953Cys), in SORL1 in 5 of 6 individuals affected by AD. Notably, variant carriers had severe AD pathology, and the SORL1 variant segregated with TDP-43 pathology (LATE-NC). We further characterized this variant and show that this Arginine substitution occurs at a critical position in the YWTD-domain of the SORL1 translation product, SORL1. Functional studies further show that the p.R953C variant leads to retention of the SORL1 protein in the endoplasmic reticulum which leads to decreased maturation and shedding of the receptor and prevents its normal endosomal trafficking. Together, our analysis suggests that p.R953C is a pathogenic variant of SORL1 and sheds light on mechanisms of how missense SORL1 variants may lead to AD.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Alzheimer Disease (AD) is the most common cause of dementia worldwide. The etiology of AD remains elusive, slowing development of disease-modifying therapies. Pathogenic variants in PSEN1, PSEN2, and APP are associated with autosomal dominantly inherited early onset AD (ADAD), although those families are rare and make up only a very small fraction of all AD. Nevertheless, knowledge gained from studying ADAD has been valuable to our understanding of the clinical, pathological, and mechanistic features of AD more broadly. Late-onset AD also has a genetic component and is known to be highly heritable, estimated at 60–80% [33] and heritability can vary with age [9]. Genome-wide association studies (GWAS) as well as genome- and exome-sequencing studies have revealed the complexity of biological processes contributing to AD risk and progression [70]. Given that families with AD likely harbor at least one AD genetic risk factor, they can provide important insight into genetic risk and disease pathogenesis.
The Sortilin-like receptor, SORL1 (protein: SORL1/SORLA), was originally identified as a member of the LDL receptor family, and the SORL1 protein is now classified as one of five mammalian sorting receptors called VPS10p receptors [31, 32, 72,73,74]. SORL1 functions as an endosomal receptor to assist cargo sorting out of the endosome to either the cell surface via the recycling pathway or to the trans-Golgi network (TGN) via the retrograde pathway [21, 24, 34, 51, 65]. For sorting of AD-related cargo, including Amyloid-β peptide (Aβ) and APP, SORL1 directly interacts with the multi-sorting complex retromer, itself highly implicated in endo-lysosomal health and neurodegeneration [18, 22, 57].
Through both candidate gene studies and GWAS, SORL1 was found to be a strong genetic risk factor for AD [42, 43, 58, 59]. Exome-sequencing studies have shown that rare loss-of-function SORL1 alleles, leading to haploinsufficiency, have been associated with highly penetrant AD [25, 26, 55, 56, 71], although the full breadth and contribution of SORL1 variants in AD is not fully defined. A large number (> 500) of SORL1 variants have been identified in patient populations with AD, but with variable levels of evidence for pathogenicity. Recently, two missense variants have been associated with autosomal dominant AD: p.(Asp1545Val) (Bjarnadottir et al., Manuscript in preparation) and p.(Tyr1816Cys) [35]. In case of the p.(Tyr1816Cys), we showed how this mutation has only minor impact on the intracellular localization per se, but strongly decreased receptor dimerization in endosomes and retromer-dependent recycling to the cell surface [35]. Reported SORL1 variants span the length of the gene and functional domains, and how different pathogenic variants impair the overall functions of SORL1 as an endosomal sorting receptor is not yet clear. It has been suggested that SORL1 maturation, which is a distinct change in some of the N-glycans attached to the luminal SORL1 domain [14], is decreased for some SORL1 missense variants [50, 60]. Defining the biochemical consequences of pathogenic SORL1 missense variants can shed light on mechanisms of disease involving SORL1 and other components of the endo-lysosomal network (ELN).
We present here a family with early onset and late-onset AD in two generations. Genetic testing confirmed a novel SORL1 variant, c.2857C > T p.Arg953Cys (R953C; NM_003105.5) which affects a residue in one of the repeats in the YWTD-domain, in 6 out of 7 affected individuals tested. Neuropathological studies demonstrated severe AD pathology, including cerebellar amyloid plaques, cortical neurofibrillary tangles, and TDP-43 deposition despite a young age of onset in most carriers of the SORL1 R953C variant. One individual, I-2, was affected with AD but did not carry the SORL1 variant and did not show TDP-43 deposition. To further characterize this genetic variant, we turned to a previously described disease-mutation domain-mapping approach that relies on identified pathogenic variants in homologous proteins including members of the LDLR family [8], to predict pathogenicity based on the domain position at which the variant occurs in SORL1. We next generated a plasmid containing the p.R953C variant and transfected it into HEK293 and N2a cells. Our in vitro studies suggest reduced SORL1 maturation and impaired endosomal localization, confirming a functional consequence of the missense variant. The influence of the variant on SORL1 cellular localization may lead to impairment of endosomal sorting and have pathogenic effects. This study adds to the growing body of literature supporting a role for SORL1 variants that may contribute to the missing AD heritability.
Methods
Study participants
The family was ascertained by the University of Washington Alzheimer Disease Research Center. The study was approved by the UW Institutional Review Board (IRB) and all participants provided written consents.
Genetic studies
Genetic analysis was performed by the Northwest Clinical Genomics Laboratory (NCGL), a CLIA certified laboratory at the University of Washington. Samples underwent next-generation exome sequencing and analysis. Libraries were constructed according to the NCGL protocol. The KAPA Hyper Prep DNA library kit (KAPA Biosystems, Wilmington, MA, USA) was used to prepare the libraries, which were subsequently enriched using an in-house, optimized xGen Exome Research Panel v1.0 (Integrated DNA Technologies, Coralville, IA, USA). Paired-end sequencing of the exome-enriched libraries was performed on a HiSeq 4000 instrument (Illumina, San Diego, CA, USA). Greater than 99% of the coding regions and canonical splice sites were sequenced to a read coverage of at least 20× or greater. The average mean depth of coverage was 144 reads. Resulting sequences were aligned to the human genome reference (hg19) using the Burrows–Wheeler Aligner (BWA) [46]. Variants were identified using the Genome Analysis Toolkit (GATK) [19, 49] and were annotated using the SnpEff annotation tool [15] in combination with various population databases and variant impact scoring tools. Individual II-5 was initially screened with a 39-gene dementia panel which included: APP, ARSA, APOE, ATP13A2, CHCHD10, CHMP2B, CSF1R, DNMT1, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, FUS, GALC, GRN, HEXA, ITM2B, LMNB1, MAPT, NOTCH3, NPC1, NPC2, OPA1, PDGFB, PDGFRB, PLP1, PRNP, PSEN1, PSEN2, SLC20A2, SLC25A12, SORL1, TARDBP, TBK1, TBP, TREM2, TYROBP, and VCP which identified the SORL1 p.R953C variant. Whole exome sequencing was then performed on II-1, II-2, II-4, and II-5 to evaluate for any other candidate variants and to investigate which variants segregated with the phenotype. Shared variants were filtered based on population data and variants with an allele frequency greater than 0.001 in ExAC were excluded from further analysis. Variants were manually evaluated through literature searches in PubMed. II-1, II-2, and II-4 were also found to carry the SORL1 p.R953C variant via exome sequencing. No other variants associated with dementing disorders were identified. II-3 was later found to carry the variant using Sanger sequencing.
APOE genotyping
APOE genotyping was performed as previously published [44]. Briefly, genomic DNA was amplified in a 9700 Gene Amp PCR System (Applied Biosystems) using primers that amplify APOE gene’s exon 4. This PCR amplicon includes both the codon 112 (ε2/ε3 vs. ε4) and codon 158 (ε2 vs. ε3/ε4) polymorphic sites.
Taqman assay: SNPs rs429358 (ε2/ε3 vs. ε4) and rs7412 (ε2 vs. ε3/ε4) were genotyped using assay C_3084793_20 and assay C_904973_10 (Thermo Fisher), respectively. All reactions were carried out in a 9700 Gene Amp PCR System with a profile of 50 °C for 5 min; 95 °C for 5 min; 50 cycles of 95 °C for 15 s, and 60 °C for 1 min.
Sanger sequencing: The PCR reaction/amplicon (1 µl) was used in BigDye sequencing reaction (Thermo Fisher) with a final volume of 10 µl. All reactions were carried out in a 9700 Gene Amp PCR System with a profile of 94 °C for 1 min; 35 cycles of 94 °C for 30 s, 55 °C for 10 s, and 60 °C for 4 min; and a final extension of 60 °C for 5 min. The PCR generated sequencing products were further purified using EDTA/ethanol precipitation and then subjected to DNA sequencing run using SeqStudio (Thermo Fisher). The sequencing data (electropherograms) were transferred and uploaded onto the Sequencher program (Genecodes) for sequence alignment.
Primer sequences:
APOE_Ex4_F: 5′ TCGGAACTGGAGGAACAACT 3′.
APOE_Ex4_R: 5′ GCTCGAACCAGCTCTTGAGG 3′.
SORL1 genotyping
SORL1 variant genotyping was performed on I-2, II-2, II-3, and III-6. Genomic DNA was amplified with Phusion Flash (Thermo Fisher) on a C1000 Touch Thermo cycler (BioRad) using primers that amplify exon 20 in SORL1. Cycle conditions: 98 °C for 10 s; 98 °C for 1 s, 65 °C for 5 s, 72 °C for 10 s X25 cycles; 72 °C for 1 min. Cleaned PCR reactions were sent for Sanger sequencing using GeneWiz (Azenta Life Sciences). Sequences were examined manually using 4 Peaks software.
Primer sequences:
SORL1 F: 5′ GCCTGGGATTTATCGGAGCA 3′
SORL1 R: 5′ TGGCATCCCTCCATAGGCT 3′.
Neuropathology
Consent for autopsy was obtained from the donor or from the legal next of kin, according to the protocols approved by the UW Institutional Review Board. At the time of autopsy, the brain was removed in the usual fashion. For patients I-2, II-2, II-3, and II-4, the left halves were coronally sectioned and samples were frozen for possible biochemical studies and the right halves were fixed in formalin. For patients II-1 and II-5, the entire brain was fixed in formalin. After fixation, the cerebrum was sectioned coronally, the brainstem was sectioned axially, and the cerebellum was sectioned sagittally.
Representative sections for histology were selected and evaluated according to National Institute of Aging-Alzheimer’s Association (NIA-AA) guidelines [52]. A microtome was used to cut 4 μm-thick tissue sections from formalin-fixed, paraffin-embedded tissue blocks. Hematoxylin and eosin (H&E), Luxol fast blue (LFB), and Bielschowsky silver-stained slides were prepared. Using previously optimized conditions, immunohistochemistry was performed using a Leica Bond III Fully Automated IHC and ISH Staining System (Leica Biosystems, Wetzlar, Germany). The sections were immunostained with mouse monoclonal antibody against paired helical filament tau (AT8, 1:1,000 dilution) (Pierce Technology, Waltham, MA), mouse monoclonal against β-amyloid (6E10, 1:5,000) (Covance, Princeton, NJ), rat monoclonal against phosphorylated TDP-43 (ser409/ser410, 1:1,000) (Millipore, Burlington, MA), and mouse monoclonal against α-synuclein (LB509, 1:500) (Invitrogen, Carlsbad, CA). Appropriate positive and negative controls were included with each antibody and each run.
Site-directed mutagenesis
The R953C variant was inserted in SORL1 pcDNA3.1 and SORL1-GFP pcDNA3.1 using site-directed mutagenesis kit (QuikChange #200521) according to manufacturers’ instruction with the following pair of primers: 5- gga tca cgt tca gtg gcc agc agt gct ctg tca ttc tgg aca acc tcc-3 and 5- gga ggt tgt cca gaa tga cag agc act gct ggc cac tga acg tga tcc-3.
Cell transfection and western blotting
Approximately 5 × 105 HEK293 and N2a cells were seeded on 6-well plates and transiently transfected with expression constructs for SORL1-WT or SORL1-R953C, using Fugene 6 Transfection Reagent kit (Promega) according to the manufacturer’s instructions. 48 h post-transfection, cell medium was changed to serum-free conditional medium and after 48 h, cells and media were harvested. Cells were lysed using lysis buffer (Tris 20 mM, EDTA 10 mM, TritonX 1%, NP40 1%). Media samples (30 ml) and lysate samples (20ug) were mixed with NuPAGE LDS sample buffer (Invitrogen, #2463558) supplemented with β-Mercaptoethanol (Sigma) and separated on SDS-PAGE using 4–12% NuPAGE Bis–Tris gels (Thermo). Proteins were then transferred to nitrocellulose membranes (Thermo) and incubated for 1 h at room temperature in Blocking buffer (Tris-Base 0.25 M, NaCl 2.5 M, skimmed milk powder 2%, tween-20 2%). Next, membranes were incubated overnight at 4 °C with LR11 antibody 1:1,000 (BDBiosciences #612633) to detect SORL1 and Beta actin 1:2000 (Sigma #A5441) as loading control, followed by three washes for 5 min in washing buffer (CaCl2 0.2 mM, MgCl2 0.1 mM, HEPES 1 mM, NaCl 14 mM, skimmed milk powder 0.2%, Tween 20 0.05%) and 1 h incubation with HRP-conjugated secondary antibody (1:1500, Dako, #P0260) for 1 h at room temperature. Membranes were washed 5 times for 5 min, incubated with FEMTO detection reagent (Thermo #34095), and visualized by iBright1500 scanner. Quantification was performed by densitometric analysis in ImageJ and data were plotted in Graphpad Prism 9.5.0.
Flow cytometry
Cell surface and total receptor level were analyzed by flow cytometry in live, transfected HEK293 and N2a cells. Briefly, HEK293 and N2a cells were transiently transfected with either SORL1-GFP-WT or SORL1-GFP-R953C plasmids. Twenty-four hours after transfection, cells were collected by trypsinization, pelleted, and resuspended in phosphate-buffered saline (PBS pH 7.4). After 15 min incubation in blocking buffer (PBS pH 7.4, 0.5% BSA), cells were immunostained at 4 °C with rabbit anti-soluble-SORL1 primary antibody followed by washing two times with PBS pH 7.4 and 30 min incubation with Alexa-flour 647 secondary antibody in the absence of detergent followed by 3 times washing and finally resuspension in FACS buffer (PBS pH 7.4, 2% FBS, 1% Glucose). Cells were analyzed by NovoCyte 3000 flow cytometer equipped with three lasers and 13 fluorescence detectors (Agilent, Santa Clara, CA). GFP and Alexa Flour 647 fluorophores were excited by the 488 and 640 nm lasers, respectively. Results were analyzed using FlowJo™ v10.8.1 Software (BD Life Sciences).
Immunocytochemistry and confocal microscopy
Approximately 5 × 104 HEK293 cells were seeded on poly-L-lysine-coated glass coverslips and transfected with expression constructs for SORL1-WT or SORL1-R953C using Fugene 6 Transfection Reagent kit (Promega). 24 h post-transfection, cells were fixed with PFA 4% for 10 min at room temperature, followed by a wash in PBS pH 7.4. Coverslips were washed twice in PBS with 0.1% Triton-X 100 (for intracellular staining) or only PBS (for membrane staining) and later blocked for 30 min at room temperature in blocking buffer (PBS, FBS 10%). Cells were then incubated overnight at 4 °C with pAb_5387 (a polyclonal rabbit serum generated for the entire SORL1 ectodomain [31]) antibody alone or with an antibody against markers specific for each intracellular compartment (EEA1 for early endosomes, TFR for recycling endosomes, and Calnexin for ER). Next, cells were washed in PBS with or without Triton-X 0.1% and incubated in Alexa Flour secondary antibodies (Invitrogen, 1:500) for 1 h at room temperature. After washing once in PBS, cells were stained with Höechst (Abcam, 1:50,000) for 10 min at room temperature. The coverslips were then mounted on glass slides using DAKO fluorescence mounting medium (Agilent) and were imaged using Zeiss LSM800 confocal microscope. Colocalization was quantified using the JACOP plugin in ImageJ software and presented as Mander’s correlation coefficient. Graphing and statistical analysis of the data were performed with GraphPad Prism 9.5.0. Antibodies used were as follows: rabbit polyclonal anti-SORL1 (pAb_5387; Aarhus University) 1:300, mouse monoclonal anti-SORL1 (mAb_AG4; Aarhus University) 1:100, anti-EEA1 (#610457 BDBiosciences) 1:100, anti-TFR 1:100 (#A-11130 Invitrogen), and anti-Calnexin (1:100) (#610523 BDBiosciences).
Statistical analysis
The data are represented as the mean ± s.d. The ‘n’ numbers represent the number of biological replicates in each experiment, while for imaging studies, ‘n’ represents the total number of cells analyzed. Data were analyzed using parametric two-tailed paired (WB analysis and flow cytometry) or unpaired (immunostaining) t tests. A P value of less than 0.05 is considered statistically significant. All statistical analysis was completed using GraphPad Prism 9.5.0 software.
Results
Clinical description
Three generations (Fig. 1) of the study family are presented here. Clinical features are reported in Table 1. Both parents (I-1 and I-2) developed late-onset dementia and I-1 also demonstrated parkinsonism and aggressive behavior. Of the 5 individuals in the II generation sibship, 4 were clinically diagnosed with AD, with a range of age of onset from 51 to 73 years. II-3 was reported to carry a clinical diagnosis of dementia prior to death and had age of onset 74 years. II-4 and II-5, identical twins, developed early onset AD at age 57 years and 51 years, respectively. II-5 developed aphasia and apraxia in addition to memory loss. III-6, daughter of II-2, developed progressive spasticity at age 44. She has also developed evidence of executive dysfunction determined by neuropsychiatric evaluation at age 45 and again on repeat testing at age 46 without progression. She has not shown any lower motor neuron findings or any other neurological signs. MRI brain did not show atrophy or other abnormality (data not shown).
Neuropathology
Individuals I-2, II-1, II-2, II-3, II-4, and II-5 were evaluated at autopsy, and findings are summarized in Table 2. Brain weight in all cases except II-1 was below the 10th percentile for age and sex [10]. Atherosclerosis was present in all cases, with plaques extending beyond the first branch point of at least one cerebral artery (defined here as moderate); in case II-4, atherosclerotic plaques were also visible on the external surface and thus graded as severe. No other abnormalities were observed grossly in any case.
Histopathology
All autopsy cases were evaluated by the standard NIA-AA protocol [30, 52]. β-Amyloid plaques progressed to the midbrain in cases I-2 and II-1 (Thal phase 4 of 5), and extended to the cerebellum in cases II-2, II-3, II-4, and II-5 (Thal phase 5 of 5, Fig. 2a). Tau tangles were present within the calcarine cortex/primary visual cortex in all cases (Braak and Braak stage VI of VI, Fig. 2b). Cortical neuritic plaque density in all cases was frequent by Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) criteria (Fig. 2c). The features in each case meet criteria for high Alzheimer’s disease neuropathologic change (ADNC) by NIA-AA guidelines [52]. Additionally, all generation II cases had TDP-43 inclusions in the amygdala and hippocampus, consistent with limbic-predominant age-related TDP-43 encephalopathy neuropathologic change (LATE-NC) stage 1 or 2 out of 3 [53] (Fig. 2d); TDP-43 inclusions were not seen in case I-2 (SORL1 variant negative). Hippocampal sclerosis was also seen in cases II-2 and II-4. Varying stages of Lewy body disease (LBD) were also identified, with diffuse (neocortical) LBD diagnosed in II-1, limbic (transitional) LBD in II-2, and brainstem-predominant LBD in II-4 (Fig. 2e). We present neuropathological findings of all subjects that underwent brain autopsy in Fig. 3.
Genetic findings
Due to early onset and family history of AD, subject II-5 underwent PSEN1 and APP research genetic testing, which was negative in both genes. Years after the subject’s passing, his genetic material was included in an early onset AD cohort evaluated by an exome panel of 39 neurodegeneration genes. II-5 was found to carry a SORL1 missense variant: NM_003105.5 c.2857C > T p.Arg953Cys (R953C). The reported allele frequency of this variant in gnomAD for those of European (non-Finnish) ancestry is 1/113646. It has not been reported in other populations assessed. In silico predictions varied; Polyphen: probably damaging, SIFT: tolerated, REVEL: 0.805, CADD v1.3: 25.4, PrimateAI: 0.633. No other pathogenic or likely pathogenic variants were identified in the other 38 genes on the neurodegeneration panel. Next, we screened II-1, II-2, II-4, and II-5 by whole exome sequencing, which revealed that all four subjects carry the SORL1 R953C variant and no other pathogenic variants known to be associated with dementia were identified. We re-confirmed the presence of the SORL1 R953C in II-2 variant using Sanger sequencing. II-3 passed away during preparation of this manuscript. We performed Sanger sequencing and confirmed the presence of the SORL1 R953C variant in II-3. Using Sanger sequencing, we found that I-2 did not carry the SORL1 variant, and no DNA samples were available from I-1. III-6 was found to carry the SORL1 variant using Sanger sequencing of dermal fibroblasts. All Sanger sequencing results are presented in Supplemental Fig. 1. C9orf72 gene expansion testing was negative in generation II and III-6. I-2, all individuals in the II generation and III-6 have an APOE ε3/ε3 genotype.
Variant characterization
The arginine residue Arg953 is located at blade position 38 of the YWTD-domain repeated sequence, located within the fifth of six repeats that build the 6-bladed β-propeller domain of SORL1 (Fig. 4a). We previously undertook a detailed disease-mutation domain-mapping approach to identify the most pathogenic sequence positions for the SORL1 domains and their risk for developing AD [8]. From this analysis, YWTD-domain sequence position 38 was identified as a high-risk site when arginine substitution occurs, and we identified variant p.Arg953His, (p.R953H) in three early onset AD patients corresponding to the same SORL1 amino acid. However, the p.R953C variant was not identified in this large exome-sequencing study [25]. From previous disease mapping work [8], we identified 5 pathogenic variants in homologous proteins corresponding to substitution of an arginine at the YWTD-domain sequence position 38, summarized in Table 3. We report variant classification by VarSome, a search engine that aggregates databases, including ClinVar, and annotates pathogenicity of variants using the ACMG/AMP guidelines [41].
Familial hypercholesterolemia (FH) is an autosomal dominant disorder with a prevalence of approximately 1 in 500 and most frequently caused by mutations in the gene for the low-density lipoprotein receptor (LDLR). The variant p.R595WLDLR has been identified in patients with FH family history in cohorts from Belgium [20] and Taiwan [13] and considered an autosomal dominant variant.
Variants in another member of the LDLR gene family, LRP5, have been associated with a number of monogenic diseases, and different variants are often the cause of different clinical disorders. The p.R1188WLRP5 has been identified to segregate in a 40-member Dutch family with three generations of early onset and late-onset cystogenesis inherited in an autosomal dominant fashion with Polycystic Liver Disease (PCLD). Cell-based studies to assess receptor activity confirmed significantly decreased activity of the mutated receptor compared to wild-type LRP5 [16].
Osteoporosis-Pseudoglioma Syndrome (OPPG) is an autosomal recessive disorder and is caused by homozygous pathogenic variants in LRP5, due to the receptor function as a key regulator of bone metabolism through the Wnt signaling pathway. The biallelic presence of the pathogenic variant p.R494QLRP5 has been identified as the cause of OPPG in families with homozygous carriers of the mutation [1, 3, 23]. Moreover, the p.R494WLRP5 that affects the same amino acid of LRP5 was identified as a potential pathogenic variant in a patient with Familial Exudative Vitreoretinopathy (FEVR), adding further support to the critical role of this amino acid to produce functional LRP5 [47].
The variant p.R752GLRP5 was also identified as the cause of disease in a compound homozygous carrier for the FEVR autosomal recessive disorder [36]. Another variant that affects the same amino acid in LRP5; p.R752WLRP5 has been reported to associate with low bone mineral density in a female heterozygous carrier, and in combination with another pathogenic LRP5 variant (p.W79R that affects a YWTD-motif residue) in her son caused a severe case of compound heterozygous OPPG [4]. Moreover, the p.R752WLRP5 was identified as a potential pathogenic variant in a patient with FEVR when it was identified in a compound heterozygous carrier together with the pathogenic p.C1305Y variants in LRP5 [27]. These studies add further support to the critical role of the arginine amino acid at domain position 38 to produce functional LRP5. A variant, p.R632HLRP4, affects the homologous receptor LRP4. This variant is causal for sclerosteosis when present as heterozygous compound mutation together with another pathogenic variant in LRP4 (p.R1170Q). Cell-based assays confirmed how both of these mutations in LRP4 reduced receptor activity, providing support of the important function of the arginine also within the YWTD-domain of LRP4 [29]. We summarize these findings and literature in Table 3.
We recently prepared a three-dimensional model of the SORL1 ectodomain including its YWTD-domain using the AlphaFold2 algorithm [34]. Here, we used this model to investigate the functional role of the arginine side chain (Fig. 4b, d). From this model, it is observed that the positively charged amino group makes ionic contacts with the side chain of the glutamic acid residue at blade-sequence position 28 (E944 of SORL1) serving to position the long arginine side chain in place to make further hydrogen bonds to two backbone carbonyls in the preceding loop between blades (Fig. 4d), thereby strongly contributing to the folding and the stability of the entire six-bladed β-propeller domain. Interestingly, in four of the five blade-sequences containing the identified disease variants, a glutamic acid is similarly located at blade-sequence position 28 (Fig. 4c).
Inspection of a larger alignment of YWTD-repeat sequences revealed that for most blade-sequences, a similar pattern is observed: when an arginine occupies blade-sequence at position 38, then a glutamate resides at blade-sequence position 28 [8], suggesting that this pair of residues may generally be important for the folding of YWTD-domains.
The crystal structures of the YWTD-domains have previously been solved for LDLR [61] and LPR4 [75], including R595LDLR and R632LRP4, the homologous residues for R953SORL1, respectively. The structure of LRP5 has not been determined, but as the crystal structure of the highly homologous LRP6 has been solved [2, 11, 12], it allowed us to use these YWTD-domain structures to gain insight in the functional role of the arginine side chain for the arginines at blade-sequence position 38 as well as for the LRP5 residues (R494LRP5/R481LRP6; R752LRP5/R739LRP6; R1188LRP5/R1178LRP6) (Fig. 4e). Indeed, we found that the arginine side chains in each of the domains are binding backbone carbonyls in the n-1 linker, and for 4 of the 5 structures, a salt bridge to a glutamic acid (at domain position 28) assists in keeping the arginine properly positioned to make the main chain interactions to the n-1 linker residue (Fig. 4e). This supports a disease mechanism where substitution of the arginine may lead to domain misfolding and destabilization in general, and importantly also for R953 of SORL1.
R953C disrupts SORL1 maturation and ectodomain shedding from the cell surface
SORL1 protein is synthesized in the ER and goes through a complex cellular process of maturation during trafficking in the ER and out of the Golgi into the ELN compartments and to the cell surface. The mature SORL1 isoform has complex-type N-glycosylations, and we previously showed only mature N-glycosylated SORL1 is shed from the cell surface to produce a fragment called soluble SORL1 (sSORL1) [14], and therefore, a decrease in sSORL1 is often a direct measure of the maturation process being decreased for folding-deficient SORL1 mutant protein. Mature SORL1 migrates more slowly by SDS-PAGE, and thus, mature and immature isoforms of cellular SORL1 can be clearly distinguished [63] (Fig. 5a).
To test whether the p.R953C variant affects SORL1 maturation and shedding, we transfected HEK293 and N2a cells with either the SORL1-WT or a SORL1-R953C construct. We performed Western blot analysis to determine the ratio of the mature to immature forms of the protein. We observed significantly decreased levels of mature SORL1 in HEK293 cells transfected with the R953C variant (Fig. 5a). We next measured the level of sSORL1 in the culture medium of HEK293 and N2a cells, transiently transfected with expression constructs for SORL1-WT or SORL1-R953C. Compared to cells transfected with a WT construct, we observed ~ 80% reduction in the sSORL1 level in the media from both the tested cell types transfected with the R953C construct (Fig. 5a, b).
R953C reduces cell surface expression of SORL1
Because we observed a significant decrease in the shedding of SORL1-R953C, we tested whether the cell surface level of SORL1 could also be affected by this variant. We transiently transfected HEK293 cells with either SORL1-WT or SORL1-R953C and first analyzed cell surface levels of SORL1 using immunocytochemistry on unpermeabilized cells, which keeps the membrane intact to allow visualization of SORL1 protein solely located at the cell membrane. Using confocal microscopy, we observed considerably fewer cells expressing SORL1 at the cell surface in cells transfected with SORL1-R953C compared to SORL1-WT (Fig. 6a). To quantitatively evaluate cell surface expression of SORL1-R953C relative to the total expression of the receptor in each individual cell, we used flow cytometry. We inserted the R953C variant into a C-terminally GFP tagged SORL1 construct, allowing for the detection of total expression of the receptor in each individual cell. We transfected both HEK293 cells and N2a cells and performed subsequent immunostaining of the transfected cells with anti-sSORL1 primary antibody and an Alexa Flour 647 secondary antibody in the absence of detergent to detect the cell surface expression of the receptor. These experiments demonstrated that more than 80% of the SORL1-R953C cells partially or completely retained SORL1 expression intracellularly compared to ~ 10–15% of the SORL1-WT cells. Results were consistent in both HEK293 and N2a cells (Fig. 6b-c).
R953C prevents SORL1 from entering the endosomal recycling pathway
The differential cell surface localization and shedding of the R953C variant compared to WT led us to next investigate for possible changes in the intracellular localization of SORL1. For these experiments, we transiently transfected HEK293 cells with either SORL1-WT or SORL1-R953C constructs. We analyzed colocalization of WT and R953C with two well-established endosomal markers, EEA1 (early endosome marker) and TFR (recycling endosome marker) and the ER marker Calnexin, 24 h post-transfection. Using confocal microscopy, we demonstrated that the colocalization of R953C is strongly reduced with both endosomal markers (Fig. 7a, b) and significantly increased in the ER (Fig. 7c). Taken together, these data suggest that the R953C variant severely disrupts the normal cellular localization trafficking of SORL1 as would be expected if the mutation leads to defective protein folding.
Discussion
SORL1 is widely recognized as a strong AD risk gene, though less is known about the AD risk attributable to rare missense variants [26, 55, 62]. Here, we describe a family with two generations of both early onset and late-onset AD in which we obtained brain autopsy pathology on 6 affected family members which enabled correlating clinical phenotype, genotype, and neuropathology. Here, we provide clinicopathological, genetic, and functional data supporting pathogenicity of a novel rare SORL1 missense variant, p.(Arg953Cys) (R953C). Five of the five offspring were found to have the SORL1 variant, and their age of onset ranged from 51 years to 74 years. Notably, all affected individuals, including the mother who was WT for SORL1 R953C, were of APOE3/3 genotype suggesting that APOE status was not contributing to risk or age of onset. Tissue from the mother (I-2) was analyzed by Sanger sequencing and found not to harbor R953C and tissue from the father was not available to confirm whether the allele was paternally inherited. Given the range of onset, it is possible that additional genetic factors inherited from either parent has influenced expression of AD in both generations. Of note, one living member of the family has been genotyped and is found to carry the variant (III-6) but is younger than the range of age of onset for the family. It is unknown whether her 3-year course of spasticity is related to the SORL1 variant or is an unrelated case of a neurologic disease.
Neuropathology examination shows the presence of severe AD pathology, including extensive plaque and neurofibrillary tangle distribution. These histologic features typically correlate with advanced clinical disease [30, 52]. There are very few studies of neuropathology on SORL1 variant carriers. There is one report of a SORL1 homozygous truncating variant (c.364C > T, p.R122*) that shows severe cerebral amyloid angiopathy in addition to AD neuropathology as well as a patient with a splicing variant (c.4519 + 5G > A) in which AD was confirmed by neuropathological studies [5]. Yet another study shows SORL1 immunoreactivity in glial cells and white matter in a family with an SORL1 variant c.3907C > T, p. R1303C [69].
In our study, all cases underwent an extensive neuropathology examination in accordance with the most up-to-date guidelines for AD and related dementias [52, 53]. In this way, we were able to identify the presence of LATE-NC, marked by accumulation of TDP-43 [53]. Interestingly, SORL1 R953C segregated with LATE-NC pathology in 5 out of 5 offspring and with earlier age at AD onset in 3 out of 5 offspring. In fact, a recent analysis linked carrying a variant in SORL1 with LATE-NC [38]. Although LATE-NC is a common co-pathology identified in AD, the underlying etiology of this TDP-43 pathology is not well understood. Age seems to be the strongest risk factor and it is most frequently noticed in individuals older than 80 years [53, 54]. Similar to other age-related neuropathologic changes, LATE-NC frequently co-occurs with other pathologies such as AD and/or hippocampal sclerosis [6], and its presence may accelerate the cognitive decline associated with these disorders [37]. It is worth acknowledging that it is possible that the co-morbid pathology of LATE-NC is driving the earlier age of onset in this family. Additionally, Lewy body disease (LBD) was frequently observed in SORL1 R953C carriers (Fig. 3). One other report in the literature has associated SNPs in SORL1 with LBD, but also implicates SNPs in APOE and BIN1 in this association as well [17]. While LBD limited to the amygdala is frequently observed in association with advanced ADNC [30, 52], ADAD due to PSEN1, PSEN2, and APP have been associated with brainstem, and limbic and diffuse LBD [45, 48] similar to what we find in this family. However, it is possible SORL1 itself contributes directly to synuclein pathology. Together, these co-pathologies suggest that SORL1 R953C may be mechanistically linked to multiple proteinopathies, clinically manifesting as AD but also impacting TDP-43 [38] and α-synuclein histopathology [17]. While SORL1 and a-synuclein have not been shown to directly interact, a-synuclein is internalized via clathrin-mediated endocytosis and is present in many arms of the endo-lysosomal network [67]. Loss of TDP-43 function affects recycling endosomes and impairs trophic signaling in neurons [64]. Therefore, while there might not be a direct interaction, dysfunction of SORL1 as an endosomal receptor that facilitates endosome sorting pathways may lead to more global impairments in endo-lysosomal network function that affect other proteins involved in neurodegeneration.
We performed analyses to examine cellular and extracellular levels of SORL1 as well as experiments to determine the localization of the R953C variant within cells. Decreased SORL1 levels are known to be pathogenic as truncation variants leading to haploinsufficiency have been definitively linked to AD [25, 26, 62]. Furthermore, human neuronal models of SORL1 deficiency show impairments in endosomal trafficking and recycling [28, 40, 51] as do neurons from minipigs with only one functional SORL1 allele [7]. One main function of SORL1 is to sort cargo from the early endosome to either the recycling pathway (cell surface) or the retrograde pathway (TGN) in conjunction with the multi-protein complex retromer [22, 66]. The cellular localization of SORL1 and the cargo it binds depend on the specific isoform: monomer vs. dimer, mature vs. immature. For protein maturation, SORL1 transits through the Golgi and the trans-Golgi network to the cell surface. Here, we demonstrate that the R953C variant of SORL1 does not undergo maturation and is not shed from the cell surface.
We have recently found that two pathogenic SORL1 missense variants associated with ADAD are located in either one of the CR-domains (Bjarnadottir et al., Manuscript in preparation) or the 3Fn-domains [35], respectively, and both display significantly impaired maturation and shedding. We have also previously observed that sSORL1 is significantly decreased in the CSF from several carriers of other established pathogenic SORL1 variants (Andersen lab, unpublished data). Furthermore, a larger screen of 70 SORL1 coding variants suggested that impaired maturation may be a common dysfunction of SORL1 mutant proteins [60].
Our study suggests that SORL1 R953C likely cannot function as a normal endosomal receptor, as it fails to enter the endosomal pathway. Instead, it is sequestered in the ER. When the receptor gets retained in the ER, it will lead to a decrease in SORL1 activity in endosomal compartments, so a direct effect of ER retention is lack-of-activity of SORL1 in the endo-lysosomal pathway. However, there could also be a gain-of-toxic-activity associated with the ER-retained misfolded receptor that potentially could lead to neurotoxic ER-stress, which is suggested to occur with certain pathogenic variants in the homologous LDLR [39, 68]. Furthermore, the ER-retained SORL1 mutant protein may have additional negative impacts on total receptor activity in the endosome and thus increase the pathogenicity of the variant. In this scenario, the mutated receptor could dimerize (or even polymerize) with the wild-type receptor, thus sequestering additional wild-type SORL1 in the ER, potentially acting via a dominant-negative mechanism in diploid cells. Structural analysis indicates that this variant occurs at a critical arginine in the YWTD β-propeller domain of SORL1 that appears to be necessary for the proper folding of the domain. When compared against homologous domains in the LDLR receptor family, arginine substitutions at this position are strongly suspected to be pathogenic.
Finally, we demonstrate that this variant likely impedes SORL1 from entering the endosomal sorting pathway. SORL1 is an endosomal receptor for many proteins that are important for proper neuronal function. We and others have shown that loss of SORL1 leads to endosomal ‘traffic jams’ and mis-localization of neurotrophic receptors and glutamate receptor subunits [51]. Loss of SORL1 in the endosomal sorting pathway will likely affect multiple aspects of neuronal health and function, contributing to neurodegeneration.
Over 500 variants in SORL1 have been identified and recent genetic studies have provided evidence as to which variants may be likely pathogenic or likely benign [25]. However, with such a large gene (encoding for more than 2200 amino acids), more variants are likely to be identified. Functional analysis of SORL1 variants will be an important tool to classify these variants based on their cellular pathogenicity and further uncover their contribution to the development of AD.
Data availability
The authors confirm that the data supporting the findings of this study are available within the article and/or its supplementary material or available from a corresponding author upon reasonable request.
References
Abdel-Hamid MS, Elhossini RM, Otaify GA, Abdel-Ghafar SF, Aglan MS (2022) Osteoporosis-pseudoglioma syndrome in four new patients: identification of two novel LRP5 variants and insights on patients’ management using bisphosphonates therapy. Osteoporos Int 33:1501–1510. https://doi.org/10.1007/s00198-022-06313-1
Ahn VE, Chu ML, Choi HJ, Tran D, Abo A, Weis WI (2011) Structural basis of Wnt signaling inhibition by Dickkopf binding to LRP5/6. Dev Cell 21:862–873. https://doi.org/10.1016/j.devcel.2011.09.003
Ai M, Heeger S, Bartels CF, Schelling DK, Osteoporosis-Pseudoglioma Collaborative G (2005) Clinical and molecular findings in osteoporosis-pseudoglioma syndrome. Am J Hum Genet 77:741–753. https://doi.org/10.1086/497706
Alonso N, Soares DC, McCloskey VE, Summers GD, Ralston SH, Gregson CL (2015) Atypical femoral fracture in osteoporosis pseudoglioma syndrome associated with two novel compound heterozygous mutations in LRP5. J Bone Miner Res 30:615–620. https://doi.org/10.1002/jbmr.2403
Alvarez-Mora MI, Blanco-Palmero VA, Quesada-Espinosa JF, Arteche-Lopez AR, Llamas-Velasco S, Palma Milla C et al (2022) Heterozygous and homozygous variants in SORL1 gene in alzheimer’s disease patients: clinical, neuroimaging and neuropathological findings. Int J Mol Sci. https://doi.org/10.3390/ijms23084230
Amador-Ortiz C, Lin WL, Ahmed Z, Personett D, Davies P, Duara R et al (2007) TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer’s disease. Ann Neurol 61:435–445. https://doi.org/10.1002/ana.21154
Andersen OM, Bogh N, Landau AM, Ploen GG, Jensen AMG, Monti G et al (2022) A genetically modified minipig model for Alzheimer’s disease with SORL1 haploinsufficiency. Cell Rep Med 3:100740. https://doi.org/10.1016/j.xcrm.2022.100740
Andersen OM, Monti G, Jensen AMG, de Waal M, Hulsman M, Olsen JG, et al. (2023) Relying on the relationship with known disease-causing variants in homologus proteins to predict pathogenicity of SORL1 variants in Alzheimer’s disease. BioRxiv. https://doi.org/10.1101/2023.02.27.524103
Baker E, Leonenko G, Schmidt KM, Hill M, Myers AJ, Shoai M et al (2023) What does heritability of Alzheimer’s disease represent? PLoS ONE 18:e0281440. https://doi.org/10.1371/journal.pone.0281440
Bell MD, Long T, Roden AC, Cooper FI, Sanchez H, Trower C et al (2022) Updating normal organ weights using a large current sample database. Arch Pathol Lab Med 146:1486–1495. https://doi.org/10.5858/arpa.2021-0287-OA
Bourhis E, Wang W, Tam C, Hwang J, Zhang Y, Spittler D et al (2011) Wnt antagonists bind through a short peptide to the first beta-propeller domain of LRP5/6. Structure 19:1433–1442. https://doi.org/10.1016/j.str.2011.07.005
Cheng Z, Biechele T, Wei Z, Morrone S, Moon RT, Wang L et al (2011) Crystal structures of the extracellular domain of LRP6 and its complex with DKK1. Nat Struct Mol Biol 18:1204–1210. https://doi.org/10.1038/nsmb.2139
Chiou KR, Charng MJ (2010) Detection of mutations and large rearrangements of the low-density lipoprotein receptor gene in Taiwanese patients with familial hypercholesterolemia. Am J Cardiol 105:1752–1758. https://doi.org/10.1016/j.amjcard.2010.01.356
Christensen S, Narimatsu Y, Simoes S, Goth CK, Vaegter CB, Small SA, et al. (2020) Endosomal trafficking is required for glycosylation and normal maturation of the Alzheimer’s-associated protein sorLA. BioRxiv. Doi https://doi.org/10.1101/2020.07.12.199885
Cingolani P, Platts A, le Wang L, Coon M, Nguyen T, Wang L et al (2012) A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3. Fly (Austin) 6:80–92. https://doi.org/10.4161/fly.19695
Cnossen WR, te Morsche RH, Hoischen A, Gilissen C, Chrispijn M, Venselaar H et al (2014) Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis. Proc Natl Acad Sci U S A 111:5343–5348. https://doi.org/10.1073/pnas.1309438111
Dai DL, Tropea TF, Robinson JL, Suh E, Hurtig H, Weintraub D et al (2020) ADNC-RS, a clinical-genetic risk score, predicts Alzheimer’s pathology in autopsy-confirmed Parkinson’s disease and Dementia with Lewy bodies. Acta Neuropathol 140:449–461. https://doi.org/10.1007/s00401-020-02199-7
Daly JL, Danson CM, Lewis PA, Zhao L, Riccardo S, Di Filippo L et al (2023) Multi-omic approach characterises the neuroprotective role of retromer in regulating lysosomal health. Nat Commun 14:3086. https://doi.org/10.1038/s41467-023-38719-8
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C et al (2011) A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 43:491–498. https://doi.org/10.1038/ng.806
Descamps OS, Gilbeau JP, Leysen X, Van Leuven F, Heller FR (2001) Impact of genetic defects on atherosclerosis in patients suspected of familial hypercholesterolaemia. Eur J Clin Invest 31:958–965. https://doi.org/10.1046/j.1365-2362.2001.00915.x
Dumanis SB, Burgert T, Caglayan S, Fuchtbauer A, Fuchtbauer EM, Schmidt V et al (2015) Distinct functions for anterograde and retrograde sorting of SORLA in amyloidogenic processes in the brain. J Neurosci 35:12703–12713. https://doi.org/10.1523/JNEUROSCI.0427-15.2015
Fjorback AW, Seaman M, Gustafsen C, Mehmedbasic A, Gokool S, Wu C et al (2012) Retromer binds the FANSHY sorting motif in SorLA to regulate amyloid precursor protein sorting and processing. J Neurosci 32:1467–1480. https://doi.org/10.1523/JNEUROSCI.2272-11.2012
Gong Y, Slee RB, Fukai N, Rawadi G, Roman-Roman S, Reginato AM et al (2001) LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. Cell 107:513–523. https://doi.org/10.1016/s0092-8674(01)00571-2
Herskowitz JH, Offe K, Deshpande A, Kahn RA, Levey AI, Lah JJ (2012) GGA1-mediated endocytic traffic of LR11/SorLA alters APP intracellular distribution and amyloid-beta production. Mol Biol Cell 23:2645–2657. https://doi.org/10.1091/mbc.E12-01-0014
Holstege H, Hulsman M, Charbonnier C, Grenier-Boley B, Quenez O, Grozeva D et al (2022) Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease. Nat Genet 54:1786–1794. https://doi.org/10.1038/s41588-022-01208-7
Holstege H, van der Lee SJ, Hulsman M, Wong TH, van Rooij JG, Weiss M et al (2017) Characterization of pathogenic SORL1 genetic variants for association with Alzheimer’s disease: a clinical interpretation strategy. Eur J Hum Genet 25:973–981. https://doi.org/10.1038/ejhg.2017.87
Hull S, Arno G, Ostergaard P, Pontikos N, Robson AG, Webster AR et al (2019) Clinical and molecular characterization of familial exudative vitreoretinopathy associated with microcephaly. Am J Ophthalmol 207:87–98. https://doi.org/10.1016/j.ajo.2019.05.001
Hung C, Tuck E, Stubbs V, van der Lee SJ, Aalfs C, van Spaendonk R et al (2021) SORL1 deficiency in human excitatory neurons causes APP-dependent defects in the endolysosome-autophagy network. Cell Rep 35:109259. https://doi.org/10.1016/j.celrep.2021.109259
Huybrechts Y, Boudin E, Hendrickx G, Steenackers E, Hamdy N, Mortier G et al (2021) Identification of compound heterozygous variants in LRP4 demonstrates that a pathogenic variant outside the third beta-propeller domain can cause sclerosteosis. Genes (Basel). https://doi.org/10.3390/genes13010080
Hyman BT, Phelps CH, Beach TG, Bigio EH, Cairns NJ, Carrillo MC et al (2012) National institute on aging-Alzheimer’s association guidelines for the neuropathologic assessment of Alzheimer’s disease. Alzheimers Dement 8:1–13. https://doi.org/10.1016/j.jalz.2011.10.007
Jacobsen L, Madsen P, Jacobsen C, Nielsen MS, Gliemann J, Petersen CM (2001) Activation and functional characterization of the mosaic receptor SorLA/LR11. J Biol Chem 276:22788–22796. https://doi.org/10.1074/jbc.M100857200
Jacobsen L, Madsen P, Moestrup SK, Lund AH, Tommerup N, Nykjaer A et al (1996) Molecular characterization of a novel human hybrid-type receptor that binds the alpha2-macroglobulin receptor-associated protein. J Biol Chem 271:31379–31383. https://doi.org/10.1074/jbc.271.49.31379
Jayadev S (2022) Genetics of Alzheimer disease. Continuum (Minneap Minn) 28:852–871. https://doi.org/10.1212/CON.0000000000001125
Jensen AMG, Kitago Y, Fazeli E, Vaegter CB, Small SA, Petsko GA et al (2023) Dimerization of the Alzheimer’s disease pathogenic receptor SORLA regulates its association with retromer. Proc Natl Acad Sci U S A 120:e2212180120. https://doi.org/10.1073/pnas.2212180120
Jensen AMG, Raska J, Fojtik P, Monti G, Lunding M, Vochyanova S, et al. (2023) The SORL1 p. Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer’s disease. MedRxiv: Doi https://doi.org/10.1101/2023.07.09.23292253
Jiao X, Ventruto V, Trese MT, Shastry BS, Hejtmancik JF (2004) Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5. Am J Hum Genet 75:878–884. https://doi.org/10.1086/425080
Josephs KA, Whitwell JL, Tosakulwong N, Weigand SD, Murray ME, Liesinger AM et al (2015) TAR DNA-binding protein 43 and pathological subtype of Alzheimer’s disease impact clinical features. Ann Neurol 78:697–709. https://doi.org/10.1002/ana.24493
Katsumata Y, Shade LM, Hohman TJ, Schneider JA, Bennett DA, Farfel JM et al (2022) Multiple gene variants linked to Alzheimer’s-type clinical dementia via GWAS are also associated with non-Alzheimer’s neuropathologic entities. Neurobiol Dis 174:105880. https://doi.org/10.1016/j.nbd.2022.105880
Kizhakkedath P, John A, Al-Sawafi BK, Al-Gazali L, Ali BR (2019) Endoplasmic reticulum quality control of LDLR variants associated with familial hypercholesterolemia. FEBS Open Bio 9:1994–2005. https://doi.org/10.1002/2211-5463.12740
Knupp A, Mishra S, Martinez R, Braggin JE, Szabo M, Kinoshita C et al (2020) Depletion of the AD risk gene SORL1 selectively impairs neuronal endosomal traffic independent of amyloidogenic APP processing. Cell Rep 31:107719. https://doi.org/10.1016/j.celrep.2020.107719
Kopanos C, Tsiolkas V, Kouris A, Chapple CE, Albarca Aguilera M, Meyer R et al (2019) VarSome: the human genomic variant search engine. Bioinformatics 35:1978–1980. https://doi.org/10.1093/bioinformatics/bty897
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC et al (2019) Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Abeta, tau, immunity and lipid processing. Nat Genet 51:414–430. https://doi.org/10.1038/s41588-019-0358-2
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C et al (2013) Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease. Nat Genet 45:1452–1458. https://doi.org/10.1038/ng.2802
Lee EG, Tulloch J, Chen S, Leong L, Saxton AD, Kraemer B et al (2020) Redefining transcriptional regulation of the APOE gene and its association with Alzheimer’s disease. PLoS ONE 15:e0227667. https://doi.org/10.1371/journal.pone.0227667
Leverenz JB, Fishel MA, Peskind ER, Montine TJ, Nochlin D, Steinbart E et al (2006) Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype. Arch Neurol 63:370–376. https://doi.org/10.1001/archneur.63.3.370
Li H, Durbin R (2009) Fast and accurate short read alignment with Burrows–Wheeler transform. Bioinformatics 25:1754–1760. https://doi.org/10.1093/bioinformatics/btp324
Li JK, Li Y, Zhang X, Chen CL, Rao YQ, Fei P et al (2018) Spectrum of variants in 389 Chinese probands with familial exudative vitreoretinopathy. Invest Ophthalmol Vis Sci 59:5368–5381. https://doi.org/10.1167/iovs.17-23541
Lippa CF, Fujiwara H, Mann DM, Giasson B, Baba M, Schmidt ML et al (1998) Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer’s disease patients with mutations in presenilin and amyloid precursor protein genes. Am J Pathol 153:1365–1370. https://doi.org/10.1016/s0002-9440(10)65722-7
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A et al (2010) The Genome analysis toolkit: a mapreduce framework for analyzing next-generation DNA sequencing data. Genome Res 20:1297–1303. https://doi.org/10.1101/gr.107524.110
Miguel L, Gervais J, Nicolas G, Lecourtois M (2023) SorLA protective function is restored by improving SorLA protein maturation in a subset of Alzheimer’s disease-associated SORL1 missense variants. J Alzheimers Dis 94:1343–1349. https://doi.org/10.3233/JAD-230211
Mishra S, Knupp A, Szabo MP, Williams CA, Kinoshita C, Hailey DW et al (2022) The Alzheimer’s gene SORL1 is a regulator of endosomal traffic and recycling in human neurons. Cell Mol Life Sci 79:162. https://doi.org/10.1007/s00018-022-04182-9
Montine TJ, Phelps CH, Beach TG, Bigio EH, Cairns NJ, Dickson DW et al (2012) National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach. Acta Neuropathol 123:1–11. https://doi.org/10.1007/s00401-011-0910-3
Nelson PT, Dickson DW, Trojanowski JQ, Jack CR, Boyle PA, Arfanakis K et al (2019) Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report. Brain 142:1503–1527. https://doi.org/10.1093/brain/awz099
Nelson PT, Lee EB, Cykowski MD, Alafuzoff I, Arfanakis K, Attems J et al (2023) LATE-NC staging in routine neuropathologic diagnosis: an update. Acta Neuropathol 145:159–173. https://doi.org/10.1007/s00401-022-02524-2
Pottier C, Hannequin D, Coutant S, Rovelet-Lecrux A, Wallon D, Rousseau S et al (2012) High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease. Mol Psychiatry 17:875–879. https://doi.org/10.1038/mp.2012.15
Raghavan NS, Brickman AM, Andrews H, Manly JJ, Schupf N, Lantigua R et al (2018) Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer’s disease. Ann Clin Transl Neurol 5:832–842. https://doi.org/10.1002/acn3.582
Reitz C (2018) Retromer dysfunction and neurodegenerative disease. Curr Genomics 19:279–288. https://doi.org/10.2174/1389202919666171024122809
Reitz C, Cheng R, Rogaeva E, Lee JH, Tokuhiro S, Zou F et al (2011) Meta-analysis of the association between variants in SORL1 and Alzheimer disease. Arch Neurol 68:99–106. https://doi.org/10.1001/archneurol.2010.346
Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F et al (2007) The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet 39:168–177. https://doi.org/10.1038/ng1943
Rovelet-Lecrux A, Feuillette S, Miguel L, Schramm C, Pernet S, Quenez O et al (2021) Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease. Acta Neuropathol Commun 9:196. https://doi.org/10.1186/s40478-021-01294-4
Rudenko G, Henry L, Henderson K, Ichtchenko K, Brown MS, Goldstein JL et al (2002) Structure of the LDL receptor extracellular domain at endosomal pH. Science 298:2353–2358. https://doi.org/10.1126/science.1078124
Scheltens P, De Strooper B, Kivipelto M, Holstege H, Chetelat G, Teunissen CE et al (2021) Alzheimer’s disease. Lancet 397:1577–1590. https://doi.org/10.1016/S0140-6736(20)32205-4
Schmidt V, Sporbert A, Rohe M, Reimer T, Rehm A, Andersen OM et al (2007) SorLA/LR11 regulates processing of amyloid precursor protein via interaction with adaptors GGA and PACS-1. J Biol Chem 282:32956–32964. https://doi.org/10.1074/jbc.M705073200
Schwenk BM, Hartmann H, Serdaroglu A, Schludi MH, Hornburg D, Meissner F et al (2016) TDP-43 loss of function inhibits endosomal trafficking and alters trophic signaling in neurons. EMBO J 35:2350–2370. https://doi.org/10.15252/embj.201694221
Simoes S, Guo J, Buitrago L, Qureshi YH, Feng X, Kothiya M et al (2021) Alzheimer’s vulnerable brain region relies on a distinct retromer core dedicated to endosomal recycling. Cell Rep 37:110182. https://doi.org/10.1016/j.celrep.2021.110182
Small SA, Kent K, Pierce A, Leung C, Kang MS, Okada H et al (2005) Model-guided microarray implicates the retromer complex in Alzheimer’s disease. Ann Neurol 58:909–919. https://doi.org/10.1002/ana.20667
Smith JK, Mellick GD, Sykes AM (2022) The role of the endolysosomal pathway in alpha-synuclein pathogenesis in Parkinson’s disease. Front Cell Neurosci 16:1081426. https://doi.org/10.3389/fncel.2022.1081426
Sorensen S, Ranheim T, Bakken KS, Leren TP, Kulseth MA (2006) Retention of mutant low density lipoprotein receptor in endoplasmic reticulum (ER) leads to ER stress. J Biol Chem 281:468–476. https://doi.org/10.1074/jbc.M507071200
Thonberg H, Chiang HH, Lilius L, Forsell C, Lindstrom AK, Johansson C et al (2017) Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene. Acta Neuropathol Commun 5:43. https://doi.org/10.1186/s40478-017-0441-9
Tosto G, Reitz C (2013) Genome-wide association studies in Alzheimer’s disease: a review. Curr Neurol Neurosci Rep 13:381. https://doi.org/10.1007/s11910-013-0381-0
Verheijen J, Van den Bossche T, van der Zee J, Engelborghs S, Sanchez-Valle R, Llado A et al (2016) A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease. Acta Neuropathol 132:213–224. https://doi.org/10.1007/s00401-016-1566-9
Willnow TE, Petersen CM, Nykjaer A (2008) VPS10P-domain receptors—regulators of neuronal viability and function. Nat Rev Neurosci 9:899–909
Yamazaki H, Bujo H, Kusunoki J, Seimiya K, Kanaki T, Morisaki N et al (1996) Elements of neural adhesion molecules and a yeast vacuolar protein sorting receptor are present in a novel mammalian low density lipoprotein receptor family member. J Biol Chem 271:24761–24768. https://doi.org/10.1074/jbc.271.40.24761
Yamazaki H, Bujo H, Saito Y (1997) A novel member of the LDL receptor gene family with eleven binding repeats is structurally related to neural adhesion molecules and a yeast vacuolar protein sorting receptor. J Atheroscler Thromb 4:20–26
Zong Y, Zhang B, Gu S, Lee K, Zhou J, Yao G et al (2012) Structural basis of agrin-LRP4-MuSK signaling. Genes Dev 26:247–258. https://doi.org/10.1101/gad.180885.111
Acknowledgements
The authors are grateful to the family whose participation made this work possible. Flow cytometry was performed at the FACS Core Facility, Aarhus University, Denmark. The authors acknowledge AU Health Bioimaging Core Facility for the use of equipment and support of the imaging facility. The authors thank the members of the University of Washington Medicine Center for Precision Diagnostics for technical support, the Geriatric Research, Education, and Clinical Center at the VA Puget Sound Health Care System, and University of Washington's Alzheimer Disease Research Center. We acknowledge Harald Frankowski in the Young lab for preparation of gDNA samples for SORL1 variant sequencing and all members of the Young lab for helpful discussions on this work.
Funding
O.M.A is supported by Novo Nordisk Foundation (#NNF20OC0064162), the Alzheimer’s Association (ADSF-21–831378-C), the EU Joint Programme-Neurodegenerative Disease Research (JPND) Working Group SORLA-FIX under the 2019 ‘‘Personalized Medicine’’ call (funded in part by the Danish Innovation Foundation and the Velux Foundation Denmark), and the Danish Alzheimer’s Research Foundation (recipient of the 2022 Basic Research Science Award). J. E. Y is supported by NIH grants R01 AG062148, K01 AG059841; an Alzheimer’s Association Research Grant 23AARG1022491; a Sponsored Research Agreement from Retromer Therapeutics and a generous gift from the Ellison Foundation (to UW). D. C. is supported by the Alzheimer’s Disease Training Program (ADTP): T32 AG052354-06A1. Clinical and pathological work is supported by the Alzheimer’s Disease Research Center (P30 AG05136).
Author information
Authors and Affiliations
Corresponding authors
Ethics declarations
Conflict of interest
O. M. A. is a consultant for Retromer Therapeutics and has equity. The other authors report no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
401_2023_2670_MOESM1_ESM.tiff
Supplementary file1. Sanger sequencing results for I-2, II-2, II-3, III-6. I-2 is C/C at SORL1 2857. II-2, II-3, III-6 are C/T at SORL1 2857. (TIF 1779 KB)
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Fazeli, E., Child, D.D., Bucks, S.A. et al. A familial missense variant in the Alzheimer’s disease gene SORL1 impairs its maturation and endosomal sorting. Acta Neuropathol 147, 20 (2024). https://doi.org/10.1007/s00401-023-02670-1
Received:
Revised:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00401-023-02670-1