Khoshdel Rad Niloofar, Aghdami Nasser, Moghadasali Reza
Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Department of Developmental Biology, University of Science and Culture, Tehran, Iran.
Front Cell Dev Biol. 2020 Mar 24;8:183. doi: 10.3389/fcell.2020.00183. eCollection 2020.
Development of the metanephric kidney is strongly dependent on complex signaling pathways and cell-cell communication between at least four major progenitor cell populations (ureteric bud, nephron, stromal, and endothelial progenitors) in the nephrogenic zone. In recent years, the improvement of human-PSC-derived kidney organoids has opened new avenues of research on kidney development, physiology, and diseases. Moreover, the kidney organoids provide a three-dimensional (3D) model for the study of cell-cell and cell-matrix interactions in the developing kidney. re-creation of a higher-order and vascularized kidney with all of its complexity is a challenging issue; however, some progress has been made in the past decade. This review focuses on major signaling pathways and transcription factors that have been identified which coordinate cell fate determination required for kidney development. We discuss how an extensive knowledge of these complex biological mechanisms translated into the dish, thus allowed the establishment of 3D human-PSC-derived kidney organoids.
后肾的发育在很大程度上依赖于肾发生区中至少四个主要祖细胞群(输尿管芽、肾单位、基质和内皮祖细胞)之间的复杂信号通路和细胞间通讯。近年来,人多能干细胞衍生的肾类器官的改进为肾脏发育、生理学和疾病的研究开辟了新的途径。此外,肾类器官为研究发育中的肾脏中的细胞间和细胞-基质相互作用提供了一个三维(3D)模型。重新创建一个具有所有复杂性的高阶且血管化的肾脏是一个具有挑战性的问题;然而,在过去十年中已经取得了一些进展。本综述重点关注已确定的协调肾脏发育所需细胞命运决定的主要信号通路和转录因子。我们讨论了如何将对这些复杂生物学机制的广泛了解转化到培养皿中,从而使得三维人多能干细胞衍生的肾类器官得以建立。