Interconversion between intestinal stem cell populations in distinct niches

Science. 2011 Dec 9;334(6061):1420-4. doi: 10.1126/science.1213214. Epub 2011 Nov 10.

Abstract

Intestinal epithelial stem cell identity and location have been the subject of substantial research. Cells in the +4 niche are slow-cycling and label-retaining, whereas a different stem cell niche located at the crypt base is occupied by crypt base columnar (CBC) cells. CBCs are distinct from +4 cells, and the relationship between them is unknown, though both give rise to all intestinal epithelial lineages. We demonstrate that Hopx, an atypical homeobox protein, is a specific marker of +4 cells. Hopx-expressing cells give rise to CBCs and all mature intestinal epithelial lineages. Conversely, CBCs can give rise to +4 Hopx-positive cells. These findings demonstrate a bidirectional lineage relationship between active and quiescent stem cells in their niches.

Publication types

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

MeSH terms

  • Animals
  • Cell Cycle
  • Cell Differentiation
  • Cell Lineage
  • Cell Proliferation
  • Cells, Cultured
  • Epithelial Cells / cytology*
  • Homeodomain Proteins / analysis
  • Homeodomain Proteins / genetics
  • Intestinal Mucosa / cytology*
  • Intestinal Mucosa / drug effects
  • Intestine, Small / cytology*
  • Intestine, Small / drug effects
  • Mice
  • Models, Biological
  • Multipotent Stem Cells / cytology*
  • Multipotent Stem Cells / physiology
  • Paneth Cells / cytology
  • Stem Cell Niche*
  • Tamoxifen / pharmacology

Substances

  • Homeodomain Proteins
  • Tamoxifen