Induction of innate immune memory via microRNA targeting of chromatin remodelling factors

Abstract

Prolonged exposure to microbial products such as lipopolysaccharide can induce a form of innate immune memory that blunts subsequent responses to unrelated pathogens, known as lipopolysaccharide tolerance. Sepsis is a dysregulated systemic immune response to disseminated infection that has a high mortality rate. In some patients, sepsis results in a period of immunosuppression (known as ‘immunoparalysis’)¹ characterized by reduced inflammatory cytokine output², increased secondary infection³ and an increased risk of organ failure and mortality⁴. Lipopolysaccharide tolerance recapitulates several key features of sepsis-associated immunosuppression⁵. Although various epigenetic changes have previously been observed in tolerized macrophages^6,7,8, the molecular basis of tolerance, immunoparalysis and other forms of innate immune memory has remained unclear. Here we perform a screen for tolerance-associated microRNAs and identify miR-221 and miR-222 as regulators of the functional reprogramming of macrophages during lipopolysaccharide tolerization. Prolonged stimulation with lipopolysaccharide in mice leads to increased expression of miR-221 and mir-222, both of which regulate brahma-related gene 1 (Brg1, also known as Smarca4). This increased expression causes the transcriptional silencing of a subset of inflammatory genes that depend on chromatin remodelling mediated by SWI/SNF (switch/sucrose non-fermentable) and STAT (signal transducer and activator of transcription), which in turn promotes tolerance. In patients with sepsis, increased expression of miR-221 and miR-222 correlates with immunoparalysis and increased organ damage. Our results show that specific microRNAs can regulate macrophage tolerization and may serve as biomarkers of immunoparalysis and poor prognosis in patients with sepsis.

Main

Lipopolysaccharide (LPS) tolerance is an immunosuppressive form of innate immune memory that can be modelled in vitro by prolonged treatment of bone-marrow-derived macrophages (BMDMs) with LPS (Extended Data Fig. 1a). As a result of this functional reprogramming of macrophages, a majority of LPS-induced genes are transcriptionally silenced (that is, tolerized) and are not expressed upon re-stimulation^7,9 (Extended Data Fig. 1b). Using this in vitro model (Extended Data Fig. 1c–e) we identified microRNAs (miRNAs) with expression patterns that correlate with tolerance (Fig. 1a). We validated these findings using qPCR (Extended Data Fig. 1f, g) and found that several miRNAs are differentially expressed during tolerance but not during an acute LPS response. Levels of miR-222, in particular, increased late during the LPS response (Extended Data Fig. 1g) and correlated with tolerance induction (Fig. 1b). miR-222 was also upregulated to a lesser extent with prolonged stimulation with tumour necrosis factor (TNF) or interleukin-1β (IL-1β) (Extended Data Fig. 1h), which has been shown to weakly induce innate immune tolerance^10,11. Pre-treatment of BMDMs with interferon gamma (IFNγ), which inhibits LPS tolerance⁸, prevented LPS-induced upregulation of miR-222 (Extended Data Fig. 1i). Although miR-221 is processed from the same primary transcript as miR-222¹², mature levels of miR-221 and of miR-222 do not always correlate (Extended Data Fig. 2a–c). Given that miR-221 is not responsive to LPS (Extended Data Fig. 2a) or IFNγ (Extended Data Fig. 2d) in BMDMs, we focused on miR-222 in BMDM experiments.

Fig. 1: miR-222 is upregulated in tolerized BMDMs and suppresses inflammatory gene expression.

a, miRNA expression in BMDMs from two mice (labelled A or B) by microarray. b, Overlay of qPCR measurement of levels of miR-222 in naive BMDMs (right axis, n = 4 biologically independent samples) and cytokine release after re-stimulation of BMDMs as in Extended Data Fig. 1c (left axis, n = 3 biologically independent samples) to show the correlation of miR-222 expression kinetics with immunosuppression. c, LPS-induced cytokine production after mimic transfection (n = 5 biologically independent samples). d–f, BMDMs (d, f) or immortalized BMDMs (e) were transduced with antagonist constructs. d, Cytokine production after stimulation of naive cells (n = 4 biologically independent samples). e, Re-stimulation of cells with fixed LPS doses after varying pre-treatment time (n = 3 independent experiments). f, Re-stimulation of cells with varying LPS doses after fixed pre-treatment time (n = 6 biologically independent samples). For all graphs, centre value represents mean, and error bars are s.e.m. P values calculated by Student’s t-test (paired, two-sided).

Source Data

BMDMs were transfected with an miR-222 mimic and stimulated with LPS to determine whether miR-222 induced reprogramming independently of other tolerogenic factors (Extended Data Fig. 2e). Overexpression of miR-222 inhibited expression of several inflammatory mediators at the protein (Fig. 1c), mRNA (Extended Data Fig. 2f), and primary transcript level (Extended Data Fig. 2g). Conversely, antagonization of miR-222 resulted in increased inflammatory gene expression, even during a naive LPS response. This effect was relatively mild early after stimulation (data not shown), probably owing to low basal levels of miR-222 expression, but increased in magnitude at later time points (Fig. 1d). To test the effect of miR-222 on tolerance, BMDMs were transduced with an miR-222 antagonist and tolerized in vitro. Antagonization of miR-222 reduced the duration and magnitude of suppression of LPS-response genes (Fig. 1e). In some cases, tolerized cells with antagonized miR-222 produced as much IL-6 or IL-12p40 in response to LPS as did non-tolerized cells (Fig. 1f).

In contrast to other genes, Tnf was suppressed at the mRNA level but not at the primary transcript level (Extended Data Fig. 2f, g), which suggests that miR-222 regulates Tnf through a mechanism that is distinct from that of other tolerized genes. Indeed, the untranslated region (UTR) of Tnf has a predicted binding site for miR-222 (Extended Data Fig. 3a). Luciferase reporter assays (Extended Data Fig. 3b) and CRISPR deletions of the predicted binding site (Extended Data Fig. 3c–g) confirmed that Tnf is a target of miR-222. However, the post-transcriptional effects of miR-222 on TNF expression do not contribute to the effects of miR-222 on other genes, as shown by the fact that TNF neutralization did not recapitulate the effects of miR-222 overexpression (Extended Data Fig. 3h, i).

Intact Tnf transcription suggested miR-222 does not alter Toll-like receptor 4 (TLR4) signalling. Indeed, miR-222 overexpression did not affect LPS-induced IκBα degradation (Extended Data Fig. 4a–c). We therefore filtered computational predictions for miR-222 targets that were expressed in macrophages, did not affect TLR4 signalling and decreased in expression late in the LPS response (between 8 and 24 h of LPS stimulation; Extended Data Table 1). This approach identified Brg1 as the target most likely to mediate the transcriptional effects of miR-222 during LPS tolerance. BRG1, a catalytic subunit of the SWI/SNF (BAF) complex, evicts polycomb repressive complexes in an ATP-dependent manner, promoting chromatin accessibility and enabling transcription factor recruitment to specific binding sites¹³. Notably, BRG1 is recruited to the promoters of late LPS-response genes, which require SWI/SNF activity for their transcription¹⁴.

The predicted miR-222–Brg1 binding site is evolutionarily conserved (Extended Data Fig. 4d), and RNA levels of Brg1 and miR-222 during the LPS response were inversely correlated (Extended Data Fig. 4e). Artificial modulation of miR-222 caused an inverse effect on Brg1 mRNA and protein levels (Extended Data Fig. 4f–h). To confirm that this was due to direct targeting, we cloned the Brg1 UTR into a luciferase reporter. miR-222 suppressed luciferase activity resulting from co-transfection in a dose-dependent manner only if the miR-222-binding site in the Brg1 UTR was intact (Extended Data Fig. 4i). We compared the effects of miR-222 overexpression on genes previously identified as being SWI/SNF-dependent in macrophages¹⁵. Overexpression of miR-222 preferentially suppressed expression of SWI/SNF-dependent genes (Fig. 2a and Extended Data Fig. 4j). Furthermore, BRG1 recruitment to inflammatory gene promoters was reduced after miR-222 overexpression (Fig. 2b). Histone H3 acetylation, which occurs downstream¹⁴ of BRG1 activity, was also reduced (Extended Data Fig. 4k). By contrast, histone H4 acetylation at these promoters, which occurs before BRG1 recruitment^16,17, was unaffected (Extended Data Fig. 4l). Finally, CRISPR–Cas9 disruption of the miR-222-binding site in the Brg1 UTR in RAW cells (Extended Data Fig. 4m) prevented miR-222-mediated suppression of some SWI/SNF-dependent genes (Extended Data Fig. 4n).

Fig. 2: miR-222 suppresses BRG1- and STAT-dependent inflammatory gene expression.

a, Comparison of miR-222 mimic transfection and theeffect of Brg1 and Brm (also known as Smarca2) knockdown¹⁵ on LPS-induced gene expression. b, ChIP in immortalized BMDMs transduced with overexpression constructs (n = 3 independent experiments; P values from Students t-test for paired values, two-sided). c, d, Schematic of treatments (c) and genes (d) analysed in e–i. Exp., expression; KO, knockout; T, tolerized. e, f, Dot plot of RNA sequencing expression values (normalized to maximal expression per gene) for wild-type (WT) and mir-221 mir-222 knockout cells (KO), top five predicted³⁴ transcription factor motifs, and statistically over-represented Gene Ontology (GO) terms (determined by PANTHER) for indicated gene groups (n = 103 gene expression values per group). Gene Ontology terms unique to de-repressed genes are highlighted in red. FKPM, fragments per kilobase per million mapped reads; TF, transcription factor. g, h, Transcription factor occupancy (g) and histone modification (h) at promoters, quantified from published ChIP–seq datasets^{20,21,22,23,24,25}. Irf8^m/m is a homozyogous mutant with the hypomorphic Irf8^R294C allele. TSS, transcription start site. i, ChIP for STAT2 occupancy in peritoneal macrophages. Values normalized to maximal binding detected for each ChIP (wild type, mir-221 mir-222 knockout n = 4 biologically independent samples; Stat1 Stat2 knockout, n = 2 biologically independent samples. P values were calculated only for wild-type versus mir-221 mir-222 knockout comparisons, by Student’s t-test, two-sided, heteroscedastic). j, Model of effect of miR-221 and miR-222 on chromatin at affected gene promoters. For all bar graphs and dot plots, centre represents mean and error bars (if present) represent s.e.m.

Source Data

To characterize the biological role of miR-222, we generated a mouse knockout model. However, miR-221 and miR-222 are encoded in the same transcript, are induced by LPS in certain cell types (Extended Data Fig. 2b, c), have similar seed sequences (Extended Data Fig. 5a), have substantial overlap in predicted mRNA targets (Extended Data Fig. 5b) and are both predicted to bind to the same target site in the Brg1 UTR (Extended Data Fig. 5c). Furthermore, as with miR-222, overexpression of miR-221 downregulates levels of Brg1 (Extended Data Fig. 5d) and has downstream effects on inflammatory gene expression (Extended Data Fig. 5e). Therefore, we targeted both miRNAs for deletion¹⁸ (Extended Data Fig. 5f–h). We then used qPCR and RNA sequencing to characterize the LPS response in mir-221 mir-222 knockout macrophages (Fig. 2c). Although the increase in Brg1 expression in peritoneal macrophages from knockout mice was modest compared to in vitro experiments, mir-221 mir-222 knockout cells expressed higher levels of many Brg1-dependent genes, as well as Tnf (Extended Data Fig. 5i, j). Some Brg1-dependent genes were more affected by mir-221 mir-222 knockout than others (compare Il6 and Nos2 in Extended Data Fig. 5j), which suggests differential sensitivity to changes in levels of BRG1.

To better understand the mechanisms of altered gene expression in cells that lack miR-221 and miR-222 (Extended Data Fig. 5k), we analysed the promoters of affected genes to identify common regulatory features. Although we obtained similar results in multiple analyses of subsets of affected genes (Extended Data Fig. 6a–f), we limited our main analysis to LPS genes that are most suppressed in tolerized wild-type cells (358 genes out of 1,036 genes in total that are responsive to LPS; Fig. 2d). Roughly half of these 358 genes were expressed at higher levels in tolerized knockout cells compared to tolerized wild-type cells (‘de-repressed’ genes, Fig. 2e), and roughly half were unaffected (‘unaffected’ genes, Fig. 2f). The promoters of de-repressed genes were enriched for the binding motifs of interferon regulatory factors (IRFs) as well as STAT1 and STAT2 (Fig. 2e), whereas those of unaffected genes were enriched for E2F and EGR family motifs (Fig. 2f). An analysis of predicted downstream functions of the de-repressed gene subset found an enrichment for IFN-response genes (Fig. 2e), and LPS-induced expression of many of these genes is reduced in Ifnar1 knockout cells¹⁹. This implies that many of these genes are a part of the late LPS response, transcribed as a result of STAT activation by autocrine and/or paracrine signalling by IFN generated from the initial LPS stimulation.

To determine whether the predicted binding motifs were used during the LPS response, we analysed transcription factor occupancy using previously published chromatin immunoprecipitation followed by sequencing (ChIP–seq) data^20,21,22,23. IRF1 and IRF8 were found to be selectively pre-associated with promoters of de-repressed genes (Fig. 2g and Extended Data Fig. 6g). However, STAT1 and STAT2 were recruited specifically to the promoters of de-repressed genes only after LPS stimulation (Fig. 2g). Other transcription factors, such as NF-κB, were not differentially recruited (Extended Data Fig. 6h). Furthermore, in cells with a deletion or mutation of Irf1 or Irf8, respectively²⁴, cytokine-induced H3K27 (histone H3, lysine 27) acetylation—a marker of active transcription—was diminished at the promoters of de-repressed genes, whereas deletion of Stat1²⁵ almost completely abolished cytokine-induced H3K27 acetylation at these genes (Fig. 2h). Consistent with this analysis, STAT2 recruitment was significantly higher at the promoters of de-repressed genes in tolerized mir-221 mir-222 knockout cells after re-stimulation, compared to wild-type cells (Fig. 2i). Furthermore, levels of Stat1 mRNA are higher in mir-221 mir-222 knockout cells and in cells in which Brg1 is overexpressed (Extended Data Fig. 7i, j) than they are in wild-type cells. Therefore, miR-221 and miR-222 perturb SWI/SNF promoter recruitment, which leads to the repression of STAT activity at inflammatory gene promoters. As BRG1 and STAT transcription factors work cooperatively only at certain gene promoters to enable IFN- and cytokine-induced gene transcription^26,27, miR-221 and miR-222 may limit expression of specific genes (Fig. 2i).

Next, we examined miR-221 and miR-222 activity using a model of sterile inflammatory shock induced by a high-dose LPS injection. In this system, changes that decrease inflammation increase survival: therefore, we used this model mainly to determine whether the anti-inflammatory effects of miR-221 and miR-222 we observe in vitro also occur in vivo. After LPS injection, levels of miR-221 and miR-222 in circulating immune cells were elevated (Fig. 3a). To determine whether this is physiologically relevant, LPS tolerance was induced in wild-type and mir-221 mir-222 knockout littermates by administering two sublethal doses of LPS before a lethal LPS dose: this regimen induces sufficient tolerance to prevent lethality in wild-type mice (Extended Data Fig. 7a, b). Although mir-221 mir-222 knockout mice were also protected from lethality, the mir-221 mir-222 knockout mice exhibited more symptoms of septic shock (Extended Data Fig. 7c), which indicates decreased anti-inflammatory effects in the knockouts. To test whether miR-221 and miR-222 contribute to survival under more extreme conditions, we used a model of septic shock in which tolerance is only partially protective against lethality (Extended Data Fig. 7d, e). In this model, absence of miR-221 and miR-222 decreased the median survival time (from 36.5 h to 20.5 h) as well as the likelihood of septic shock survival over a 72-h period (Fig. 3b).

Fig. 3: miR-221 and miR-222 protect against inflammatory septic shock but increase susceptibility to live infection in mice.

a, miRNA levels in blood buffy coat 24 h after LPS injection (n = 7 mice for dose 0, 7 mice for dose 8 mg per kg and 9 mice for dose 12 mg per kg). b, Survival of littermates that were untreated or tolerized before lethal LPS injection, as in Extended Data Fig.. c, d, Bacterial dissemination (c, n = 6 wild-type and 8 knockout mice) and host survival (d) after intraperitoneal injection with S. Typhimurium. e, Model of miR-221 and miR-222 effect on the immune response and host survival during the course of sepsis. For a, c, P values were determined by Student’s t-test (paired, two-sided). P values for b, d, log-rank (Mantel–Cox) test (performed only for n > 3). For all dot plots, centre line represents mean; error bars represent s.e.m.

Source Data

Although LPS-induced septic shock is used to study acute inflammation in vivo, this model does not recapitulate sepsis in patients or necessarily predict the effect of inflammatory regulators on patient outcome. Therefore, to study the role of miR-221 and miR-222 in a model that better reflects the systemic innate response to pathogen challenge, we used a Salmonella enterica subsp. enterica serovar Typhimurium (S. Typhimurium) infection model. First, we performed in vitro assays using green fluorescent protein (GFP)-expressing S. Typhimurium to infect BMDMs. BMDMs from mir-221 mir-222 knockout mice exhibited increased GFP per cell soon after infection (Extended Data Fig. 7f–h). At later time points, this difference was not observed (Extended Data Fig. 7h), which suggests that—despite increased phagocytosis—mir-221 mir-222 knockout cells are more efficient at suppressing intracellular replication and/or survival. We confirmed this finding by lysing BMDMs and comparing bacterial colony-forming unit (CFU) recovery at early and late time points after infection (Extended Data Fig. 7i). To test miR-221 and miR-222 effects in vivo, wild-type and knockout mice were injected intraperitoneally with the same strain of S. Typhimurium. Two days after infection, fewer bacterial CFUs were recovered from the liver and spleen of mir-221 mir-222 knockout mice (Fig. 3c). In addition, mir-221 mir-222 knockout mice exhibited increased survival time (Fig. 3d), suggesting that the loss of miR-221 and miR-222 confers resistance to bacterial replication and/or dissemination. These findings suggest that miR-221 and miR-222 broadly suppress inflammation and innate immune function. During the early stages of sepsis expression of miR-221 and miR-222 may be protective, by limiting the excessive inflammatory cytokine production that contributes to septic shock. Conversely, miR-221 and miR-222 appear to contribute to immunoparalysis, and increased miR-221 and miR-222 expression may enhance lethality during the later stages of sepsis (Fig. 3e).

Because it is unclear which models most accurately resemble conditions in patients, we next examined miR-221 and miR-222 expression in human disease. Consistent with results from mouse cells, miR-221 and miR-222 are both upregulated in response to prolonged LPS stimulation of a human monocyte-like cell line, whereas only miR-222 is upregulated by LPS in this cell line after phorbol 12-myristate 13-acetate (PMA)-induced differentiation to a macrophage-like cell type (Extended Data Fig. 8a, b). Next we analysed miR-221 and miR-222 expression in three patient cohorts. In the first cohort (Extended Data Fig. 8c), we quantified miR-221 and miR-222 levels in peripheral blood mononuclear cells from ten sequential patients from an intensive care unit, who met sepsis criteria²⁸ within 4 h of admission to the intensive care unit. Compared to peripheral blood mononuclear cells from healthy donors, miR-221 and miR-222—but not several other inflammation-associated miRNAs—were significantly higher in samples from patients in the intensive care unit (Fig. 4a). Levels of miR-221 and miR-222 expression were then examined in a second cohort of patients, all of whom had acute decompensated liver disease and clinical suspicion of infection (Extended Data Fig. 8d). Patients with organ failure, as defined by the chronic liver failure–sequential organ failure assessment, had significantly higher levels of miR-222 than patients without such failure (Fig. 4b). Levels of miR-221 correlated with those of miR-222 (Extended Data Fig. 8f), but were not increased to statistically significant levels (Fig. 4c). Levels of miR-222 in this cohort inversely correlated with levels of BRG1 expression (Fig. 4d). In a set of matched peripheral blood mononuclear cell and serum samples, levels of miR-222 and TNF were also inversely correlated (Fig. 4e). Finally, the inverse correlation between miR-222 and BRG1 was also observed in CD14⁺ monocytes sorted from the peripheral blood mononuclear cell population of a third clinical cohort (Fig. 4f and Extended Data Fig. 8e), confirming changes in levels of miR-222 and BRG1 in myeloid cells.

Fig. 4: miR-222 correlates with immunosuppression and severe sepsis in patients.

a, miRNA expression in peripheral blood mononuclear cells from healthy donors (H) or patients (P) from the intensive care unit with sepsis (n = 10 per group). P values, two-sided Mann–Whitney U test. b, c, Expression in peripheral blood mononuclear cells from a cohort of patients with chronic liver disease, stratified for bacterial infection (n = 20 patients negative (−), 10 positive (+)) and inflammation-related organ failure (acute-on-chronic liver failure; n = 15 patients per group). P values, two-sided Mann–Whitney U test. Bact., cells from patients with bacterial infection; organ, cells from patients with organ failure. d, f, Correlation of RNA levels in peripheral blood mononuclear cells (d, n = 28 patients) or CD14⁺ monocytes of patients with multiple organ failure (f, n = 10 patients). Spearman’s rho (ρ) and P values from bivariate non-parametric regression analysis. e, Correlation of serum TNF and miR-222 expression in peripheral blood mononuclear cells (PBMC) from four patients with signs of infection. Two patients had organ failure according to the EASL CLIF-C criteria for acute-on-chronic liver failure. In box and whisker plots, median is shown as centre line; box, 25th to 75th percentiles; whiskers, minimum to maximum values. NS, not significant.

Source Data

Unlike generalized inflammatory markers, miR-222 elevation correlates specifically with severe sepsis. miR-222 levels do not correlate with inflammatory markers such as C-reactive protein or white blood cell count, but showed a significant correlation with organ-damage markers, including creatinine and the model for end-stage liver disease score (Extended Data Fig. 8g–j). miR-222 expression may be a useful biomarker for detecting patients who are undergoing septicaemia-induced immunoparalysis and are, therefore, predisposed to organ failure and mortality.

In summary, our data establish a model in which miR-221 and miR-222 restrict chromatin remodelling and silence transcription to enforce innate immune tolerance. After prolonged innate immune signalling, increased expression of miR-221 and miR-222 reduces expression of BRG1, which leads to changes in SWI/SNF complex levels or composition that result in the selective expression of only those LPS-response genes with the most favourable chromatin states. The fact that substantial changes in gene expression result from modest miR-221- and miR-222-dependent changes in BRG1 expression is consistent with previous reports that the mutation or deletion of a single allele of the SWI/SNF subunit is sufficient to confer strong phenotypic effects^29,30. Hence, by fine-tuning the levels of BRG1, miR-221 and miR-222 can prevent prolonged expression of STAT-dependent inflammatory genes in macrophages, thereby leading to tolerance or innate immunoparalysis (Extended Data Fig. 9). By contrast, robust activation of STAT1—for example, by co-stimulation with IFNγ—can block⁸ or even reverse^31,32 LPS tolerance and innate immunoparalysis. Consistent with such a role for STAT1, treatment with IFNγ has been shown to improve outcomes in sepsis³³.

Although LPS tolerance promotes survival in mouse models of sterile shock, patients with sepsis probably succumb to primary or secondary¹ infections owing to immunosuppression as a result of functional reprogramming of myeloid cells. Thus, the same innate immunoparalysis that is protective in the mouse LPS-shock model would be responsible for organ damage and mortality in human patients with sepsis. We identify miR-221 and miR-222 as mediators of tolerance and show that miR-221 and miR-222 expression may distinguish patients with organ failure who are at high risk of mortality from those patients with infection alone. Thus, the monitoring of miR-221 and miR-222, or related bio-markers, may help clinicians to stratify patients with sepsis into groups on the basis of whether they would benefit from pro-inflammatory immunotherapies or classical anti-inflammatory treatments.

Methods

Cell culture

RAW 264.7 cells (ATCC TIB-7) were cultured in DMEM supplemented with 10% fetal bovine serum. 293FT cells (Invitrogen R7007) and L-929 cells (ATCC CCL-1) were cultured in DMEM supplemented with 10% fetal bovine serum. Cells were purchased from vendor and tested for mycoplasma contamination before use (no further authentication of line identity was performed). L-cell conditioned medium (LCM) was generated by filter-sterilizing the supernatant of L-929 cells that were allowed to grow for one week in culture. Primary BMDMs were generated by isolation and culture of mouse bone marrow in complete RPMI supplemented with 20% LCM for up to 12 days. Immortalization of BMDMs was performed as previously described³⁵ by inoculation with the J2 retrovirus. For cell stimulations, 10 ng/ml LPS (Sigma L8274), 10 ng/ml recombinant human TNF (R&D Systems 210-TA), 100 ng/ml recombinant mouse IL-1β (R&D Systems 401-ML-005), 100 ng/ml recombinant mouse IFNγ (BD Pharmingen 554587), 10 pg/ml recombinant mouse IL-10 (eBioScience 88-7104-ST), 10 μM dexamethasone (Sigma D402) and 0.01 μM oestrogen (Sigma E2758) were used unless otherwise indicated. For tolerization experiments, BMDMs were stimulated with 10 ng/ml LPS for 15 h (or as indicated), washed 5 times with 1× PBS, then allowed to rest for 2 h in LPS-free complete medium supplemented with 20% LCM. BMDMs were then stimulated with 1 μg/ml LPS for 4 h (for qPCR) or 12 h (for enzyme-linked immunosorbent assay (ELISA)), or as indicated.

miRNA microarray

Samples were treated as described, rinsed with 1× PBS, lysed in TRIzol and sent to a commercial microRNA array profiling service (Exiqon). As part of the service, samples were labelled using the miRCURY Hy3/Hy5 Power labelling kit and hybridized on the miRCURY LNA array (v.11.0 hsa, mmu and rno). All capture probes for the control spike-in oligonucleotides produced signals in the expected range. The quantified background-corrected signals were normalized using the global Lowess (locally weighted scatterplot smoothing) regression algorithm, and a list of differentially expressed miRNAs was returned.

miRNA mimic and antagonist oligonucleotides

Pre-miR miRNA precursors (Ambion AM17100) and anti-miR miRNA inhibitors (Ambion AM17000) were transfected into BMDMs to modulate miRNA function in short-term experiments. Part numbers for oligonucleotides are as follows: for overexpression experiments, pre-miR negative control #1 (Invitrogen AM17110), miR-222-3p (PM11376), miR-221-3p (PM10337); for antagonization experiments, anti-miR miRNA negative control #1 (Ambion AM17010), miR-222-3p (AM11376), miR-221-3p (AM10337). To optimize transfection conditions, the FAM dye-labelled pre-miR negative control #1 (Invitrogen AM17121) oligonucleotide was used. Transfection of 50,000 BMDMs per well of a 12-well plate with 6 μl lipofectamine and 0.1 nmol oligonucleotide diluted in 200 μl of Opti-MEM (total) was found to provide transfection of >80% of cells (as measured by flow cytometry), and these conditions were used for all further experiments in BMDMs. Medium was replaced with complete RPMI containing 20% LCM after 4 h to minimize cytotoxicity. Cells were allowed to recover for 24–48 h before stimulation.

Production of virus and BMDM transduction

Plasmids for miRNA overexpression (GeneCopoeia CmiR0001-MR01, MmiR3289-MR01, or MmiR3434-MR01) or antagonization (GeneCopoeia CmiR-AN0001-a.m.03 or HmiR-AN0399-a.m.03) were transfected into 293FT cells with the Lenti-Pac HIV Expression Packaging Kit (GeneCopoeia HPK-LVTR-20) or Lenti-Pac FIV Expression Packaging Kit (GeneCopoeia FPK-LVTR-20) to generate viral particles. BMDMs were inoculated by spin infection in 6-well plates in the presence of 6 μg/ml polybrene (Sigma H9268). Following spin inoculation, viral supernatant was immediately replaced with complete RPMI supplemented with 20% LCM. Cells were allowed to recover overnight. For primary BMDMs, plating for inoculation was generally performed on day five of differentiation. The first spin infection was performed on day six, second spin infection (if necessary) was performed on day seven, and plating for experiments was performed on day eight.

ELISA

BMDMs were plated at 50,000 cells per well, and cytokine concentrations in cell supernatants were measured using the BD OptEIA Mouse IL-6 ELISA Set (BD 555240), BD OptEIA Mouse IL-12 (p40) ELISA Set (BD 555165), or BD OptEIA Mouse TNF (Mono/Mono) ELISA Set (BD 555268) according to the manufacturer’s instructions.

RNA extraction, reverse transcription and qPCR

Total RNA was extracted from samples using TRIzol reagent (Invitrogen 15596018). For reverse transcription and detection of miRNAs, the Universal cDNA Synthesis Kit (Exiqon 203301) and locked nucleic acid primers (Exiqon) were used. For other genes, approximately 1 μg of RNA was reverse transcribed with SuperScript III (Invitrogen 18080085). qPCR was then performed with VeriQuest Fast SYBR (Affymetrix 75675). The amplified transcripts were quantified using the comparative C_t method.

Computational prediction of miRNA-binding sites

miR-222-binding sites were predicted using the PITA algorithm³⁶ (http://genie.weizmann.ac.il/pubs/mir07/mir07_prediction.html) or MicroCosm Targets program (which utilizes the miRanda algorithm) as indicated in the text. MicroCosm Targets Version 5 was used to search for targets for mmu-miR-222³⁷. UTRs and miRNA sequences were manually input to the PITA algorithm, and default search settings were used. All predictions were re-verified with their respective programs on 5 December 2013.

Construction of reporter vectors and luciferase reporter assays

The Brg1 UTR was amplified from IMAGE clone 30533489 (Open Biosystems MMM1013-9498346) and cloned into the pMIR-Report (Ambion AM5795) multiple cloning site using HindIII and SpeI restriction sites. The Tnf UTR was amplified from cDNA generated from BMDMs stimulated with LPS for 1 h, and inserted into the pMIR-Report vector as performed for the Brg1 UTR. Reporter plasmids were transfected into 293FT cells along with a Renilla luciferase reporter (used to normalize for transfection efficiency). After 24 h, Firefly and Renilla luciferase activity was quantified using the Dual-Luciferase Reporter Assay (Promega E1980).

CRISPR

The CRISPR design tool (http://crispr.mit.edu) was used to design guide RNAs for cloning into the PX458 (Addgene 48138) and PX459 (Addgene 48139) dual Cas9 and single-guide RNA expression plasmids³⁸ to generate plasmids to target identified miR-222-binding sites for deletion. Cells were transiently transfected with empty vector or targeting vectors. After 24 h, transfected cells were selected using 48 h of puromycin treatment (PX459) or by sorting for GFP positive (PX458) cells. Limiting dilution was performed to isolate clonal cell lines. Clones were screened for appropriate deletion by PCR. Deletion of targeted regions was confirmed by sequencing when necessary. Gene expression was compared between lines with successful deletion, unsuccessful deletion and lines generated by transfection with expression plasmids that lacked a Cas9-targeting sequence.

For deletion of the miR-222-binding site in the Tnf UTR, the following guide sequences were used: combination 1, TCAGCGTTATTAAGACAATT GGG and ATTACAGTCACGGCTCCCGT GGG; combination 2, TTGTCTTAATAACGCTGATT TGG and ATTTCTCTCAATGACCCGTA GGG. For deletion of the miR-222-binding site in the Brg1 UTR, the following guide sequences were used: GGAGTAGCCCTTAGCAGTGA TGG and ACCAGATGTAGTTTCGAACT TGG.

Intracellular staining for flow cytometry

Cells were rinsed and fixed for 15–30 min at room temperature in 4% paraformaldehyde. Cells were rinsed and permeabilized by resuspension in 5% saponin for 10–20 min at room temperature. Either anti-IκBα (L35A5, Cell Signaling 4814), anti-Brg1 (H88, Santa Cruz sc-10768), or rabbit monoclonal antibody IgG isotype control (Cell Signaling 3900) was added, and cells were incubated for an additional 20 min at room temperature. Cells were rinsed and re-suspended in saponin with 1:300 dilution of fluorochrome-conjugated secondary antibody (Alexa Fluor 488 donkey anti-rabbit IgG, Invitrogen A21206; Alexa Fluor 546 goat anti-rabbit IgG, Invitrogen A11010; or Alexa Fluor 546 donkey anti-mouse IgG, Invitrogen A10036). After incubation at room temperature for 20 min, cells were rinsed, re-suspended in PBS and analysed on a BD LSRII flow cytometer.

Chromatin immunoprecipitation

Cells from a 15-cm plate were fixed by incubation in 1% formaldehyde for 5 min, rinsed and lysed by incubation for 5 min on ice in buffer L1 (50 mM Tris at pH 9, 2 mM EDTA, 0.1% NP-40, 10% glycerol, with protease inhibitors). Nuclei were spun down and re-suspended in 500 μl buffer L2 (50 mM Tris at pH 8, 0.1% sodium dodecyl sulphate and 5 mM EDTA). Sonication was performed in a Bioruptor, using 10 cycles of 30 s each. Immunoprecipitation was performed using 20 μl magnetic protein A beads and 5 μg anti-acetyl-histone H4 (Lys5; Millipore 07-327), 2 μg anti-BRG1 (H-88; Santa Cruz sc-10768), or 5 μg anti-acetyl-histone H3 (Millipore 06-599) per 50 μl of chromatin in a 500 μl volume. After overnight rotation at 4 °C, supernatant was isolated. DNA was recovered from the supernatant by adding 20 μl of 5 M NaCl, 50 μl of 10% SDS and 5 μl of proteinase K, shaking for 2 h at 60 °C (unbound fraction). Beads were washed 3× in high salt buffer (20 mM Tris at pH 8.0, 0.1% SDS, 1% NP-40, 2 mM EDTA, and 0.5 M NaCl), and 3× in Tris–EDTA. DNA was eluted from beads by re-suspending beads in 100 μl elution buffer and shaking for 2 h at 60 °C (bound fraction). Bound and unbound fractions were heated to 95 °C for 10 min. DNA was purified from fractions using the Qiagen PCR Purification Kit (28104). To check for promoter binding, qPCR was performed using DNA from the bound and unbound fractions. Bound:unbound ratios were normalized to alpha-crystallin ratios, as this should represent a silent gene.

Amaxa nucleofection

BMDMs were nucleofected with 2 μg of plasmid DNA using the Amaxa Mouse Macrophage Nucleofector Kit (VPA-1009), in conjunction with the Amaxa Nucleofector II Device, according to the manufacturer-optimized protocol.

Salmonella enterica serovar Typhimurium infection

For these experiments, a GFP-expressing Salmonella enterica serovar Typhimurium strain (SL1344) was used. S. Typhimurium cultures were grown in LB medium supplemented with 100 μg/ml carbenicillin and 30 μg/ml streptomycin. Overnight cultures were diluted and allowed to grow for an additional hour before use, to ensure bacteria were in log-growth phase. OD_{600 nm} readings were correlated to previously determined CFU values and used to quantify number of bacteria present in culture. BMDMs were infected by inoculation of DMEM growth medium (containing only streptomycin) with bacteria at a multiplicity of infection of 50. Plates were spun at 800 r.c.f. for 5 min at 4 °C. BMDMs were incubated for 30 min at 37 °C. Cells were washed 3 times, and then incubated in medium containing gentamycin (100 μg/ml for incubations of 2 h or less, 12 μg/ml for longer incubations). BMDMs were subsequently analysed for GFP content by flow cytometry, or lysed in water to enable plating of lysate dilutions on LB agar plates containing carbenicillin to determine bacterial CFU counts.

Mice

For BMDM generation, female C57Bl/6J mice of 7–10 weeks of age were used, unless otherwise noted. For tolerance and septic shock experiments, male C57Bl/6J mice of 6–10 weeks of age were used. LPS (Escherichia coli O55:B5; Sigma L2880) and d-(+)-galactosamine hydrochloride (Sigma G0500) were re-suspended in sterile PBS and filter-sterilized before intraperitoneal injection. For in vivo infection experiments, mice were given intraperitoneal injections of 1 × 10⁷ CFUs per kg of a GFP-expressing Salmonella enterica serovar Typhimurium strain (SL1344) suspended in PBS. Mice were maintained under specific-pathogen-free conditions in animal facilities at Columbia University Medical Center. All animal experiments were carried out with the approval of the Columbia University Institutional Animal Care and Use Committee, and in compliance with regulations and guidelines set forth by Columbia University.

Generation of knockout mice

mir-221 mir-222 knockout mice were generated at the Columbia University Transgenic Mouse facility. In brief, KV1 (129B6 hybrid) ES cells were electroporated with the linearized targeting construct discussed in Extended Data Fig. 6. After positive and negative selection, clonal cell lines were screened by PCR for proper integration of the construct. Positive lines were expanded, blastocyst injection was performed and germline transmission was confirmed. mir-221 mir-222 knockout mice were backcrossed to the C57Bl/6 background 5–8 times before experimental use.

Peritoneal macrophage isolation

Five millilitres of cold PBS was injected into the peritoneal cavity of euthanized mice. The peritoneum was gently massaged. Fluid was collected and the process was repeated. Cell suspension was spun down and cells were plated at 500,000 cells per well in 12-well plates. Macrophages were allowed to adhere overnight. Non-adherent cells were rinsed off with PBS washes.

Thioglycollate elicitation of peritoneal macrophages

Three per cent thioglycollate was sterilized and aged for at least two months. One millilitre of thioglycolate preparation was injected into the peritoneal cavity of each mouse five days before the isolation of macrophages (as described in ‘Peritoneal macrophage isolation’).

Monocyte isolation

Bones were isolated from wild-type C57Bl6/J mice. Marrow was retrieved by crushing. Monocytes were purified using the EasySep Mouse Monocyte Isolation Kit.

RNA sequencing

RNA sequencing was performed by the JP Sulzberger Columbia Genome Center. Poly-A pull-down was used to enrich mRNAs from total RNA samples (200 ng–1 μg per sample, RIN > 8 required). Libraries were prepared using the Illumina TruSeq RNA prep kit. Libraries were then sequenced using Illumina HiSeq2000. Multiplexed and pooled samples were sequenced to a depth of 24–34 × 10⁶ reads per sample as 100-bp single-end reads. RTA (Illumina) was used for base calling, and bcl2fastq (version 1.8.4) was used for converting BCL to fastq format, coupled with adaptor trimming. Reads were mapped to a reference genome (mouse: UCSC/mm9) using Tophat (version 2.1.0) with 4 mismatches (–read-mismatches = 4) and 10 maximum multiple hits (–max-multihits = 10). To tackle the mapping issue of reads that are from exon–exon junctions, Tophat infers novel exon–exon junctions ab initio and combines them with junctions from known mRNA sequences (refgenes) as the reference annotation. The relative abundance (also known as the expression level) of genes and splice isoforms were estimated using cufflinks (version 2.0.2) with default settings.

ChIP–seq analysis

Track data of genes of interest were loaded into Galaxy³⁹ (http://usegalaxy.org) using the UCSC table browser and mouse mm10 genome. Using Galaxy, previously published ChIP–seq data^{20,21,22,23,24,25} was then aligned to the mouse mm10 genome using the HISAT program (Galaxy version 2.03) with default settings. BamCoverage (Galaxy version 2.3.6.0) was then used to generate a coverage bigwig file, using default settings to scale to the size of the mm9 mouse genome. ComputeMatrix (Galaxy version 2.3.6.0) and plotHeatmap (Galaxy version 2.3.6.0) were then used to compare transcription factor occupancy at gene promoters, using the transcription start site as the reference point.

Dataset references

ChIP–seq data that were analysed were from the European Nucleotide Archive accession ERA319838 (IRF5), and from the following Gene Expression Omnibus accessions: GSE56123²⁰ (IRF1, IRF8, STAT1, STAT2); GSE67343²¹ (IRF3); GSE36104²² (IRF2, IRF4, NF-κB subunits); GSE62697²³ (IRF7); GSE77886²⁴ (IRF mutants); and GSE38379²⁵ (STAT1 knockout).

Patient sample selection and processing

We selected 10 consecutive patients, newly admitted to a medical or surgical intensive care unit (ICU), who had systemic inflammatory response syndrome and a known or suspected infection⁴⁰. Patients were excluded from the study if they had an ICU admission or bacteraemia within the previous 30 days. After obtaining informed consent from the patient or a surrogate, whole blood was drawn within 4 h of ICU admission. Peripheral blood mononuclear cells were isolated from whole blood of healthy human volunteers or buffy coat isolates from patients from the ICU meeting sepsis criteria, by centrifugation on a Ficoll cushion. RNA was isolated with the miRNeasy micro kit (Qiagen 217084) and reverse transcribed as in ‘RNA extraction, reverse transcription and qPCR’. Experiments were performed with approval of the Institutional Review Board at Columbia University and in accordance with regulations and guidelines set forth by the university. The results of these experiments are shown in Fig. 4a.

Patient sample selection and processing

Additional patient cohorts were obtained from hospitalized patients with acute decompensation of chronic liver disease and suspected bacterial infection. Baseline characteristics and outcome of patients with decompensated liver disease in the absence or presence of multiple organ failure syndrome (according to the EASL CLIF-C criteria for acute-on-chronic liver failure⁴¹) are given in Extended Data Fig. 8. Clinical scores—such as model for end-stage liver disease scores, bacterial culture count, protein analysis, blood count and serum levels of C-reactive protein and creatinine—were obtained from routine laboratory analysis. The determination of serum concentration of TNF was performed by ELISA. The results of these experiments are shown in Fig. 4b–f.

The isolation and characterization of human immune cells and the use of clinical data was approved by the internal review board (ethics committee of the Jena University Hospital, no. 3683-02/3). The study conformed to the ethical guidelines of the 1975 Declaration of Helsinki, and patients granted written informed consent before inclusion.

Statistics and sample collection

Student’s t-tests were performed using the T.TEST function in Microsoft Excel. All other statistical tests were performed using Prism software. Unless otherwise stated, two-sided tests were performed. For samples using cell lines and cells isolated from inbred mice, the Student’s t-test was often used. The distributional requirements for the test are assumptions. This means that—for instance—under the assumption of normal-distributed residuals, the t-test is an exact test. However, given a non-normal distribution of cell line data the test is not exact, but is instead approximative. For patient samples, nonparametric tests were used to avoid the assumption of a normal distribution. In all figures, error bars represent s.e.m. unless otherwise indicated. Standard deviations and s.e.m. values were calculated for each group of data and used to estimate variation (s.e.m. values are shown as error bars in most experiments). Variation generally appears similar between groups being compared. All experiments were replicated in the laboratory at least two times. Unless otherwise indicated, in experiments using primary cells n represents the number of experiments performed with separate cell isolations; in experiments using immortalized cells or cell lines, n represents the number of experiments performed using separate cell populations. Systematic randomization and blinding were not performed. Samples were excluded from the analysis if they were identified as outliers using the Grubbs’ test (also known as the extreme studentized deviate method).

For mouse LPS-shock studies, an appropriate sample size was estimated on the basis of an outcome variable of survival time, measured in hours. An estimate was based on using a one-tailed Student’s t-test to determine statistical significance. Control mice were expected to succumb within 62 h. Knockout mice were expected to become moribund 52 h after LPS injection at the latest. Therefore, the minimal effect size was estimated to be 10 h. On the basis of the literature and experiments previously performed by our laboratory, we anticipated a standard deviation of 10 h. Taking into account a power of 80% and alpha of 0.05, we calculated a sample size of 10 mice per genotype.

Reporting summary

Further information on experimental design is available in the Nature Research Reporting Summary linked to this paper.

Data accessibility

RNA sequencing data that support the findings of this study have been deposited in Gene Expression Omnibus (https://www.ncbi.nlm.nih.gov/geo/) with the accession code GSE89918. All other data are available from the corresponding author upon reasonable request.

Extended data figures and tables

Extended Data Fig. 1 In vitro modelling of tolerance and miR-222 induction upon prolonged LPS stimulation.

a, Schematic of experiments performed in b. b, Expression of LPS-response genes in control BMDMs that have undergone the given treatments. Four major expression patterns of LPS-response genes in response to tolerization were noted (n = 5 biologically independent samples). c, Schematic of experiments performed in d. d, Cytokine production—measured by ELISA—by BMDMs re-stimulated with LPS overnight after pre-treatment with LPS for the given periods of time. Time points chosen for miRNA microarray analysis have bars shaded in grey (n = 3 biologically independent samples). e, Schematic of strategy for experiments performed in Fig. 1. f, Comparison of microarray (x axis) and qPCR (y axis) measurements of LPS-induced upregulation of miRNAs. A linear regression showing the correlation between the two methods is plotted (n = 16 miRNAs tested). g, qPCR verification of LPS-induced change in expression of nine miRNAs (n = 3 biologically independent samples). h, Expression of miR-222 after stimulation of BMDMs by anti-inflammatory and tolerance-inducing factors for the given lengths of time (n = 5 biologically independent samples; Dex, dexamethasone). i, Expression of miR-222 in response to LPS alone, or LPS after pre-treatment of BMDMs with IFNγ (n = 4 biologically independent samples). For all bar and line graphs, mean ± s.e.m. is plotted. *P < 0.05, **P < 0.01, determined by two-sided Student’s t-test for paired values.

Extended Data Fig. 2 Differential regulation of miR-222 and miR-221 and association of miR-222 with in vitro tolerance.

a–c, Expression of miR-221 and miR-222 in response to LPS stimulation of BMDMs (a, n = 4 biologically independent samples), peritoneal macrophages (b, n = 3 biologically independent samples for miR-222 and n = 4 biologically independent samples for miR-221) or monocytes isolated from the bone marrow (c, n = 3 biologically independent samples), as determined by qPCR. d, LPS-induced miR-221 and miR-222 expression in BMDMs with or without IFNγ pre-treatment, as determined by qPCR (n = 2 biologically independent samples). e, Schematic of experiments performed in f, g and Fig. 1c. f, g, LPS-induced gene expression at the mRNA (f) or primary transcript (g) level after miR-222 mimic transfection (n = 5 biologically independent samples). For all bar and line graphs, mean ± s.e.m. is plotted. *P < 0.05, **P < 0.01, determined by two-sided Student’s t-test for paired values.

Extended Data Fig. 3 Tnf is a direct target of miR-222, but suppression of Tnf does not account for miR-222-mediated transcriptional silencing of late LPS-response genes.

a, Sequence and prediction scores of an miR-222-binding site in the Tnf UTR. b, Activity of a luciferase reporter construct in which the luciferase coding sequence is followed by either the complete Tnf UTR, or a UTR in which the predicted miR-222-binding site has been mutated to the sequence shown in a (n = 6 independent experiments). c, CRISPR–Cas9 targeting strategy to delete predicted binding sites. CDS, coding sequence. d, Clones of RAW cells were screened for successful deletion of the miR-222-binding site by PCR across the targeted region of the UTR, using genomic DNA from the given clonal line as a template. Screening for Tnf UTR deletion is shown. Experiment was repeated twice with similar results. e, Successful deletion of the miR-222-binding site in RAW cell clones was confirmed by sequencing genomic DNA of the given cell line. miR-222-binding site in the Tnf UTR is highlighted in yellow. f, LPS-induced Tnf expression in control and CRISPR–Cas9-targeted RAW cells (n = 4 independent experiments). g, Average effect of miR-222 mimic transfection on LPS-induced Tnf mRNA levels in either control mouse embryonic fibroblasts or mouse embryonic fibroblasts that have undergone CRISPR targeting and clonal selection for deletion of the miR-222-binding site. Average of the effects from the three clonal lines (n = 3 independent experiments) is shown. h, Wild-type BMDMs were transfected with a control or miR-222 mimic oligonucleotide. Twenty-four hours later, cells were pre-treated with an isotype control (IgG) or TNF-neutralizing (anti-TNF) antibody for two hours, and stimulated with 10 ng ml⁻¹ LPS. Expression of the given genes was measured by qPCR (n = 4 biologically independent samples). i, Efficacy of TNF neutralization was confirmed by treating cells with IgG or anti-TNF as above, followed by stimulation with 100 ng ml⁻¹ recombinant mouse TNF (n = 3 biologically independent samples). Gene upregulation was not detected (ND) in two out of three samples treated with anti-TNF. For all bar graphs, mean ± s.e.m. is plotted. *P < 0.05, **P < 0.01, determined by two-sided Student’s t-test for paired values.

Extended Data Fig. 4 Evidence of miR-222 targeting of Brg1.

a, Example of gating used to exclude dead cells from flow cytometry analyses in c, g and Extended Data Fig. 6i. b, Example of gating used to distinguish cells with high versus low levels of IκBα, as analysed in c. c, Effect of miRNA overexpression (by viral transduction) on LPS-induced IκBα degradation in immortalized BMDMs, measured by flow cytometry (n = 4 independent experiments). d, Sequence and prediction scores of an miR-222-binding site in the Brg1 UTR. e, miR-222 and Brg1 mRNA levels in LPS-stimulated BMDMs (n = 3 biologically independent samples). f, Brg1 mRNA levels in resting BMDMs 24 h after transfection (n = 4 biologically independent samples). g, Effect of miRNA overexpression or antagonization (by viral transduction) on BRG1 levels in immortalized BMDMs, observed by flow cytometry. Representative of four independent experiments with similar results, quantified in h. h, Flow cytometry analysis of BRG1 protein levels in transduced immortalized BMDMs (n = 4 independent experiments). i, Activity of a luciferase reporter construct in which the luciferase coding sequence is followed by either the complete Brg1 UTR, or a UTR in which the predicted miR-222-binding site has been mutated to the sequence shown in d (n = 3 independent experiments). j, Quantification of the average effect of miR-222 mimic transfection on Brg1-dependent and Brg1-independent LPS-response genes (n = 3 biologically independent samples). Two-sided Student’s t-test for heteroscedastic values used to compare ratios (ratio of miR-222 overexpression to control) at peak LPS-induced expression times for Brg1-dependent versus Brg1-independent genes. k, l, ChIP for histone H3 acetylation (k) or histone H4 acetylation (l) after LPS stimulation of immortalized BMDMs transduced with overexpression constructs (k and l tested in same n = 3 independent experiments). m, Successful deletion of the miR-222-binding site in the Brg1 UTR in RAW cell clones was confirmed by sequencing genomic DNA of the given cell line. miR-222-binding site is highlighted in yellow. n, Effect of miR-222 overexpression (by oligonucleotide transfection) on LPS-induced gene expression in either a RAW cell line in which the Brg1–miR-222 binding site was deleted by CRISPR targeting (as shown in Extended Data Fig. 3c) or a cell line in which the binding site was not targeted for deletion (n = 5 independent experiments). For all bar graphs, mean ± s.e.m. is plotted. *P < 0.05, **P < 0.01, determined by two-sided Student’s t-test for paired values.

Extended Data Fig. 5 Comparison of miR-221 and miR-222, and effects of miR-221 and miR-222 deletion on the transcriptional response to LPS.

a, Alignment of the mature miR-221 and miR-222 sequences. The miRNA seed sequence is highlighted in yellow. b, Venn diagram displaying overlap between MicroCosm target predictions for mmu-miR-221 and mmu-miR-222. c, Alignment and computational scores of miR-221 sequence with predicted Brg1 UTR target site. Alignment of miR-222 sequence with the site is also shown. d, Brg1 expression in BMDMs transfected with the given oligonucleotide (n = 3 biologically independent samples). e, LPS-induced cytokine production in BMDMs transfected with given miRNA mimics, as measured by ELISA (n = 5 biologically independent samples). f, Schematic of the miR-221 and miR-222 locus after targeting with a construct designed to generate both complete and conditional mir-221 mir-222 knockout mice. g, Schematic of the miR-221 and miR-222 locus after breeding targeted mice (f) with EIIa-Cre mice, which results in complete deletion of miR-221 and miR-222. h, miRNA expression in BMDMs from littermates with a wild-type or mir-221 mir-222 knockout allele (n = 5 biologically independent samples). i, LPS-induced gene expression in naive or tolerized peritoneal macrophages isolated from wild-type or mir-221 mir-222 knockout littermates (n = 7 biologically independent samples). j, Heat map comparing the effect of Brg1 and Brm knockdown¹⁵ and mir-222 knockout on gene expression. Colours represent values of the given ratios; red indicates increased expression, white indicates no change and blue indicates decreased expression. k, Heat map of LPS-induced gene expression in wild-type and mir-221 mir-222 knockout macrophages. For all bar graphs, mean ± s.e.m. is plotted. *P < 0.05, **P < 0.01, determined by two-sided Student’s t-test for paired (d, e) or heteroscedastic (i) values.

Extended Data Fig. 6 Gene Ontology and ChIP–seq analysis shows that genes affected by mir-221 mir-222 knockout have differential gene functions and transcription-factor binding at promoters.

a–f, Enriched GO terms (a–c) and transcription-factor binding at promoters (d–f) of genes that are expressed at higher (twofold or higher) or lower (0.5-fold or lower) levels in mir-221 mir-222 knockout macrophages after no stimulation (a, d, n = 647 genes higher, 565 genes lower), LPS stimulation (b, e, n = 143 genes higher, 121 genes lower) or LPS tolerization followed by re-stimulation (c, f, n = 123 genes higher,48 genes lower). PANTHER was used to identify GO terms. The top four terms for each category are shown; GO terms that are unique to either higher- or lower-expression gene subsets are highlighted. g, h, IRF and NF-κB subunit occupancy at gene promoters; gene subsets analysed are described in Fig. 2h. For transcription factor analyses, previously published ChIP–seq data were used^{20,21,22,23,24,25}. i, RNA levels of genes in wild-type or mir-221 mir-222 knockout peritoneal macrophages, quantified by a single RNA sequencing experiment. j, qPCR for gene expression in wild-type BMDMs after Amaxa-based nucleofection of given overexpression construct (n = 3 biologically independent samples). For all bar graphs, centre value represents the mean and errors bars (if applicable) represent s.e.m.

Extended Data Fig. 7 mir-221 mir-222 knockout mice have an altered LPS response and knockout macrophages exhibit enhanced Salmonella uptake and clearance in vitro.

a, Schematic of experiments performed in b, c. b, Survival of naive or tolerized mice injected with high doses of LPS. c, Wild-type or mir-222 knockout littermates were tolerized to LPS before lethal LPS injection. The change in body temperature after final LPS injection was monitored for 24 h. d, Schematic of experiments performed in e. e, Survival of naive or tolerized mice injected with LPS and d-galactosamine. f, BMDMs from wild-type or mir-221 mir-222 knockout mice were spin-infected with a GFP-expressing strain of S. Typhimurium. Fluorescence was analysed by microscopy 60 min after infection. Representative of two independent experiments with similar results. g, BMDMs from wild-type or mir-221 mir-222 knockout mice were spin-infected with a GFP-expressing strain of S. Typhimurium. Fluorescence was analysed by flow cytometry 30 min post-infection. Representative of three independent experiments with similar results. h, Average fluorescence of infected BMDMs after early (left) or late (right) time points after infection (n = 4 biologically independent wild-type samples, 3 biologically independent knockout samples). i, Survival of S. Typhimurium after in vitro infection of BMDMs, determined by comparing CFUs after lysis of BMDMs at early and late time points of infection (n = 5 biologically independent wild-type samples, 4 biologically independent knockout samples). For all bar and line graphs, mean ± s.e.m. is plotted. *P < 0.05, **P < 0.01, determined by two-sided Student’s t-test for heteroscedastic values.

Extended Data Fig. 8 miR-221 and miR-222 are upregulated in human cells and patients with sepsis.

a, b, LPS-induced miRNA expression in undifferentiated (a) or phorbol 12-myristate 13-acetate-differentiated (b) human U937 cells (n = 3 independent experiments). c, Patient characteristics for data shown in Fig. 4a. APACHE, acute physiology and chronic health evaluation; SAPS, simplified acute physiology score. Categorical variables are given as n (percentage in parentheses) and continuous variables as median (interquartile range in parentheses). d, e, Baseline characteristics of patients with decompensated liver disease in the absence or presence of multiple organ failure syndrome (according to the EASL CLIF-C criteria for acute-on-chronic liver failure). Data in d correspond to peripheral blood mononuclear cell analyses (Fig. 4b–d). Median with interquartiles or frequencies and percentages are shown. P values from Mann–Whitney U test or Fisher’s exact test as appropriate (two-sided). *, comparing any infection to no infection; **, 4 out of 30 (13%) and 1 out of 10 (10%) patients were lost to follow-up within 30 days. Data in e correspond to monocyte analyses (Fig. 4f). Median with interquartiles or frequencies and percentages are shown. P values from Mann–Whitney U test or Fisher’s exact test as appropriate (two-sided). *, comparing any infection to no infection; **, 1 out of 10 (10%) patients was lost to follow-up within 30 days. f, Correlation between miR-221 and miR-222 levels in patients characterized in d (n = 30 patients). Bivariate nonparametric correlation analysis (Spearman’s rho) was used to identify correlations between variables and P values. g–j, Linear correlation of miR-222 expression and C-reactive protein (g), white blood cell count (h), creatinine levels (i) or model for end-stage liver disease score (j) in samples from the patient cohort described in d (n = 30 patients). Bivariate nonparametric correlation analysis (Spearman’s rho) was used to identify correlations between variables and P values. For line graphs, mean ± s.e.m. is plotted.

Extended Data Fig. 9 Model of the effect of miR-222 on LPS-induced macrophage tolerance.

a, Before an acute LPS stimulation, chromatin at BRG1-dependent gene promoters prevents binding of remodelling-dependent transcription factors and RNA polymerase. b, After an acute LPS stimulation, transcription factors such as STAT1 and STAT2 are recruited to gene promoters and stabilize BRG1 binding. c, d, BRG1 activity leads to chromatin remodelling (c), which enables recruitment of additional transcription factors, such as NF-κB, to the unwound DNA (d). This enables polymerase recruitment and licensing, which leads to gene transcription. e, After an initial LPS response, chromatin is ‘reset’ to an inhibitory state by negative regulators of chromatin accessibility. f, Upon LPS re-stimulation, transcription factors must again be recruited to gene promoters. However, miR-222 limits the level of BRG1. g, Lack of available BRG1 prevents chromatin remodelling at many gene promoters, and prevents downstream transcription factor recruitment. This prevents gene transcription from occurring in most cells.

Extended Data Table 1 Identification of targets of miR-222

Source Data

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