Conserved and Divergent Molecular and Anatomic Features of Human and Mouse Nephron Patterning

J Am Soc Nephrol. 2018 Mar;29(3):825-840. doi: 10.1681/ASN.2017091036. Epub 2018 Feb 15.

Abstract

The nephron is the functional unit of the kidney, but the mechanism of nephron formation during human development is unclear. We conducted a detailed analysis of nephron development in humans and mice by immunolabeling, and we compared human and mouse nephron patterning to describe conserved and divergent features. We created protein localization maps that highlight the emerging patterns along the proximal-distal axis of the developing nephron and benchmark expectations for localization of functionally important transcription factors, which revealed unanticipated cellular diversity. Moreover, we identified a novel nephron subdomain marked by Wnt4 expression that we fate-mapped to the proximal mature nephron. Significant conservation was observed between human and mouse patterning. We also determined the time at which markers for mature nephron cell types first emerge-critical data for the renal organoid field. These findings have conceptual implications for the evolutionary processes driving the diversity of mammalian organ systems. Furthermore, these findings provide practical insights beyond those gained with mouse and rat models that will guide in vitro efforts to harness the developmental programs necessary to build human kidney structures.

Keywords: human genetics; kidney development; nephron.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins
  • Cell Differentiation*
  • Cell Lineage
  • Gene Expression Profiling
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Humans
  • Immunohistochemistry
  • Lymphoid Enhancer-Binding Factor 1 / genetics
  • Lymphoid Enhancer-Binding Factor 1 / metabolism
  • Mice
  • Nephrons / embryology*
  • Nephrons / metabolism*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Stem Cells / metabolism
  • Stem Cells / physiology*
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Wnt4 Protein / metabolism

Substances

  • Apoptosis Regulatory Proteins
  • CITED1 protein, human
  • Cited1 protein, mouse
  • Homeodomain Proteins
  • LEF1 protein, human
  • Lef1 protein, mouse
  • Lymphoid Enhancer-Binding Factor 1
  • Nerve Tissue Proteins
  • Nuclear Proteins
  • SIX2 protein, human
  • Six2 protein, mouse
  • Trans-Activators
  • Transcription Factors
  • WNT4 protein, human
  • Wnt4 Protein
  • Wnt4 protein, mouse