The New York Stem Cell Foundation Research Institute, New York, NY, USA.
Methods Mol Biol. 2022;2454:455-471. doi: 10.1007/7651_2021_359.
Microglia, the immune cells of the central nervous system (CNS), play critical roles in CNS homeostasis and disease. Mounting evidence has linked aberrant microglial functions to neurodevelopment, neuroinflammatory and neurodegenerative diseases, underlining the need for novel models to investigate human microglia biology. Here we describe a protocol for generating in vitro patient-specific microglia progenitors and microglia-like cells from induced pluripotent stem cells (iPSCs). Our protocol generates microglia progenitor cells in approximately 35 days, which then can further mature into microglia-like cells within two additional weeks. Microglia differentiation is driven by specific growth factors and cytokines in serum-free conditions, resulting in mesodermal progenitors that grow in a monolayer which releases free-floating microglia progenitors. Isolated progenitors can be used in co-culture systems with other neuronal cells, xenotransplanted to generate chimeric mouse models, or further differentiated into adherent microglia-like cells for functional studies.
小胶质细胞是中枢神经系统(CNS)的免疫细胞,在 CNS 稳态和疾病中发挥着关键作用。越来越多的证据表明,异常的小胶质细胞功能与神经发育、神经炎症和神经退行性疾病有关,这凸显了需要新型模型来研究人类小胶质细胞生物学。在这里,我们描述了一种从诱导多能干细胞(iPSC)生成体外患者特异性小胶质细胞祖细胞和小胶质样细胞的方案。我们的方案大约需要 35 天才能生成小胶质细胞祖细胞,然后再经过两周的时间进一步成熟为小胶质样细胞。小胶质细胞分化是由无血清条件下的特定生长因子和细胞因子驱动的,导致中胚层祖细胞在单层中生长,释放游离的小胶质细胞祖细胞。分离的祖细胞可用于与其他神经元细胞的共培养系统中,异种移植以生成嵌合小鼠模型,或进一步分化为贴壁的小胶质样细胞进行功能研究。