Conserved and Divergent Features of Human and Mouse Kidney Organogenesis

器官发生 肾脏发育 生物 进化生物学 计算生物学 细胞生物学 遗传学 基因 胚胎干细胞
作者
Nils O. Lindström,Jill A. McMahon,Jinjin Guo,Tracy Tran,Qiuyu Guo,Elisabeth A. Rutledge,Riana K. Parvez,Gohar Saribekyan,Robert Schuler,Christopher Liao,Albert D. Kim,Ahmed Abdelhalim,Seth Ruffins,Matthew E. Thornton,Laurence Basking,Brendan H. Grubbs,Carl Kesselman,Andrew P. McMahon
出处
期刊:Journal of The American Society of Nephrology [American Society of Nephrology]
卷期号:29 (3): 785-805 被引量:194
标识
DOI:10.1681/asn.2017080887
摘要

Human kidney function is underpinned by approximately 1,000,000 nephrons, although the number varies substantially, and low nephron number is linked to disease. Human kidney development initiates around 4 weeks of gestation and ends around 34-37 weeks of gestation. Over this period, a reiterative inductive process establishes the nephron complement. Studies have provided insightful anatomic descriptions of human kidney development, but the limited histologic views are not readily accessible to a broad audience. In this first paper in a series providing comprehensive insight into human kidney formation, we examined human kidney development in 135 anonymously donated human kidney specimens. We documented kidney development at a macroscopic and cellular level through histologic analysis, RNA in situ hybridization, immunofluorescence studies, and transcriptional profiling, contrasting human development (4-23 weeks) with mouse development at selected stages (embryonic day 15.5 and postnatal day 2). The high-resolution histologic interactive atlas of human kidney organogenesis generated can be viewed at the GUDMAP database (www.gudmap.org) together with three-dimensional reconstructions of key components of the data herein. At the anatomic level, human and mouse kidney development differ in timing, scale, and global features such as lobe formation and progenitor niche organization. The data also highlight differences in molecular and cellular features, including the expression and cellular distribution of anchor gene markers used to identify key cell types in mouse kidney studies. These data will facilitate and inform in vitro efforts to generate human kidney structures and comparative functional analyses across mammalian species.

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