Cycling Lgr5+ stem cells fuel the rapid turnover of the adult intestinal epithelium. The existence of quiescent Lgr5+ cells has been reported, while an alternative quiescent stem cell population is believed to reside at crypt position +4. Here, we generated a novel Ki67RFP knock‐in allele that identifies dividing cells. Using Lgr5‐GFP;Ki67RFP mice, we isolated crypt stem and progenitor cells with distinct Wnt signaling levels and cell cycle features and generated their molecular signature using microarrays. Stem cell potential of these populations was further characterized using the intestinal organoid culture. We found that Lgr5high stem cells are continuously in cell cycle, while a fraction of Lgr5low progenitors that reside predominantly at +4 position exit the cell cycle. Unlike fast dividing CBCs, Lgr5low Ki67− cells have lost their ability to initiate organoid cultures, are enriched in secretory differentiation factors, and resemble the Dll1 secretory precursors and the label‐retaining cells of Winton and colleagues. Our findings support the cycling stem cell hypothesis and highlight the cell cycle heterogeneity of early progenitors during lineage commitment.
A Ki67‐RFP knock‐in allele highlights the heterogeneity of Lgr5+ stem‐ and progenitor cells based on in vivo cell cycle profiles.
Ki67‐RFP allele allows identification and visualization of proliferating cells in vivo.
Lgr5high intestinal stem cells are continuously in the cell cycle.
Quiescent Lgr5low “+4” cells are secretory precursors.
The EMBO Journal (2014) 33: 2057–2068
- Received January 25, 2014.
- Revision received June 18, 2014.
- Accepted July 10, 2014.
- © 2014 The Authors. Published under the terms of the CC BY NC ND 4.0 license
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