Interconversion between intestinal stem cell populations in distinct niches.

Journal:

Science 2011 Dec

Authors:

Takeda N, Jain R, LeBoeuf MR, Wang Q, Lu MM, Epstein JA

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.
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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.[less]

Mesh Headings:

Animals, Cell Cycle, Cell Differentiation, Cell Lineage, Cell Proliferation, Cells, Cultured, Epithelial Cells, Homeodomain Proteins, Intestinal Mucosa, Intestine, Small, Mice, Models, Biological, Multipotent Stem Cells, Paneth Cells, Stem Cell Niche, Tamoxifen