Naderlinger Elisabeth, Murphy Cormac, Feifel Elisabeth, Jennings Paul, Gstraunthaler Gerhard, Wilmes Anja
Department of Chemistry and Pharmaceutical Sciences, Division of Molecular and Computational Toxicology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Division of Physiology, Medical University Innsbruck, Innsbruck, Austria.
Methods Mol Biol. 2025;2924:45-57. doi: 10.1007/978-1-0716-4530-7_4.
Within the glomerulus, podocytes are highly specialized visceral epithelial cells, that are part of the glomerular filtration barrier. Human podocyte cell culture is rather challenging for primary or immortalized cells, due to the non-proliferative state of the cells. In addition, de-differentiation is often observed rapidly. Hence, iPSC-derived podocytes offer an exciting alternative to culture podocyte-like cells from different donors over a prolonged time. Here we report an improved protocol of a simple and rapid one-step differentiation that drives iPSC into podocyte-like cells in 10 days and offers the possibility to transfer the podocyte-like cells into another plate format once.
在肾小球内,足细胞是高度特化的脏层上皮细胞,是肾小球滤过屏障的一部分。由于细胞的非增殖状态,人足细胞的原代或永生化细胞培养颇具挑战性。此外,常常很快就会观察到细胞去分化。因此,诱导多能干细胞(iPSC)衍生的足细胞为长时间培养来自不同供体的足细胞样细胞提供了令人兴奋的替代方法。在此,我们报告了一种改进的方案,该方案采用简单快速的一步分化法,可在10天内将iPSC诱导为足细胞样细胞,并提供了将足细胞样细胞转移到另一种平板形式的可能性。