Abstract
The identification of stem/progenitor cells within the retinal neural environment has opened up the possibility of therapy via cellular replacement and/or reprogramming of resident cell populations (1–4). Within the neuro-retinal niche, following injury or in disease states (including inflammation and degeneration), cellular responses affect tissue homeostasis, reduce cell density, disrupt tissue architecture, and produce scar formation. Microglia (resident retinal immune cell tissue macrophage) are key to the maintenance of retinal homeostasis and are implicated in responses that may influence the control and behavior of retinal progenitors (5, 6). Factors to consider in the generation of a transplantable cell resource with good migratory and integrative capacity include their yield, purity, and functional viability. Utilizing human postmortem retina, we have created a research platform to isolate, culture, and characterize adult retinal microglia as well as analyze their effect on retinal progenitors. Here, we describe techniques using magnetic labeled bead cell separation to isolate pure populations of retinal CD133+ precursor cells and CD11b+ microglia from primary adult retinal cell suspensions (RCSs), enabling flow cytometric cell phenotypic and qPCR genotypic analysis, as well as functional analysis by real-time ratiometric calcium imaging.
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Acknowledgments
This work was supported by grants from Guide Dogs for the Blind (Dr Debra Carter) and The Dr Hans and Mrs Gertrude Hirsch Studentship via the National Eye Research Council (NERC), UK (Balini Balasubramaniam). We are grateful to the Bristol Eye bank team, and most of all to the tissue donors and their families.
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Carter, D.A., Balasubramaniam, B., Dick, A.D. (2012). Functional Analysis of Retinal Microglia and Their Effects on Progenitors. In: Weber, B., LANGMANN, T. (eds) Retinal Degeneration. Methods in Molecular Biology, vol 935. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-080-9_19
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DOI: https://doi.org/10.1007/978-1-62703-080-9_19
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