Invasion of distal nephron precursors associates with tubular interconnection during nephrogenesis

J Am Soc Nephrol. 2012 Oct;23(10):1682-90. doi: 10.1681/ASN.2012030283. Epub 2012 Aug 16.

Abstract

Formation of a functional renal network requires the interconnection of two epithelial tubes: the nephron, which arises from kidney mesenchyme, and the collecting system, which originates from the branching ureteric epithelium. How this connection occurs, however, is incompletely understood. Here, we used high-resolution image analysis in conjunction with genetic labeling of epithelia to visualize and characterize this process. Although the focal absence of basal lamina from renal vesicle stages ensures that both epithelial networks are closely apposed, we found that a patent luminal interconnection is not established until S-shaped body stages. Precursor cells of the distal nephron in the interconnection zone exhibit a characteristic morphology consisting of ill-defined epithelial junctional complexes but without expression of mesenchymal markers such as vimentin and Snai2. Live-cell imaging revealed that before luminal interconnection, distal cells break into the lumen of the collecting duct epithelium, suggesting that an invasive behavior is a key step in the interconnection process. Furthermore, loss of distal cell identity, which we induced by activating the Notch pathway, prevented luminal interconnection. Taken together, these data support a model in which establishing the distal identity of nephron precursor cells closest to the nascent collecting duct epithelium leads to an active cell invasion, which in turn contributes to a patent tubular interconnection between the nephron and collecting duct epithelia.

Publication types

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

MeSH terms

  • Animals
  • Cell Movement
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / metabolism
  • Female
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Imaging, Three-Dimensional
  • Kidney / embryology*
  • Kidney / metabolism
  • Kidney Tubules, Distal / embryology
  • Kidney Tubules, Distal / metabolism
  • Male
  • Mice
  • Mice, Transgenic
  • Microscopy, Confocal
  • Nephrons / embryology
  • Nephrons / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Zonula Occludens-1 Protein / metabolism

Substances

  • Homeodomain Proteins
  • Six2 protein, mouse
  • Tjp1 protein, mouse
  • Transcription Factors
  • Zonula Occludens-1 Protein
  • Green Fluorescent Proteins