Robert Schuler

Conserved and Divergent Features of Human and Mouse Kidney Organogenesis

TitleConserved and Divergent Features of Human and Mouse Kidney Organogenesis
Publication TypeJournal Article
Year of Publication2018
AuthorsN. O. Lindström, J. A. McMahon, J. Guo, T. Tran, Q. Guo, E. Rutledge, R. K. Parvez, G. Saribekyan, R. E. Schuler, C. Liao, A. D. Kim, A. Abdelhalim, S. W. Ruffins, M. E. Thornton, L. Basking, B. Grubbs, C. Kesselman, and A. P. McMahon
JournalJournal of the American Society of Nephrology
Pages785–805
Abstract

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.

URLhttps://jasn.asnjournals.org/content/29/3/785
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