WNT-SHH Antagonism Specifies and Expands Stem Cells prior to Niche Formation

Cell. 2016 Jan 14;164(1-2):156-169. doi: 10.1016/j.cell.2015.11.058.

Abstract

Adult stem cell (SC) maintenance and differentiation are known to depend on signals received from the niche. Here, however, we demonstrate a mechanism for SC specification and regulation that is niche independent. Using immunofluorescence, live imaging, genetics, cell-cycle analyses, in utero lentiviral transduction, and lineage-tracing, we show that in developing hair buds, SCs are born from asymmetric divisions that differentially display WNT and SHH signaling. Displaced WNT(lo) suprabasal daughters become SCs that respond to paracrine SHH and symmetrically expand. By contrast, basal daughters remain WNT(hi). They express but do not respond to SHH and hence maintain slow-cycling, asymmetric divisions. Over time, they become short-lived progenitors, generating differentiating daughters rather than SCs. Thus, in contrast to an established niche that harbors a fixed SC pool whose expelled progeny differentiate, asymmetric divisions first specify and displace early SCs into an environment conducive to expansion and later restrict their numbers by switching asymmetric fates.

Publication types

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

MeSH terms

  • Animals
  • Cell Division
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism
  • Hair Follicle / cytology*
  • Hair Follicle / metabolism
  • Hedgehog Proteins / metabolism*
  • Mice / embryology*
  • Microscopy, Fluorescence
  • SOX9 Transcription Factor / metabolism
  • Stem Cells / cytology*
  • Stem Cells / metabolism*
  • Wnt Signaling Pathway*

Substances

  • Hedgehog Proteins
  • SOX9 Transcription Factor
  • Sox9 protein, mouse