Cycling Stem Cells Are Radioresistant and Regenerate the Intestine

Cell Rep. 2020 Jul 28;32(4):107952. doi: 10.1016/j.celrep.2020.107952.


A certain number of epithelial cells in intestinal crypts are DNA damage resistant and contribute to regeneration. However, the cellular mechanism underlying intestinal regeneration remains unclear. Using lineage tracing, we show that cells marked by an Msi1 reporter (Msi1+) are right above Lgr5high cells in intestinal crypts and exhibit DNA damage resistance. Single-cell RNA sequencing reveals that the Msi1+ cells are heterogeneous with the majority being intestinal stem cells (ISCs). The DNA damage-resistant subpopulation of Msi1+ cells is characterized by low-to-negative Lgr5 expression and is more rapidly cycling than Lgr5high radiosensitive crypt base columnar stem cells (CBCs). This enables an efficient repopulation of the intestinal epithelium at early stage when Lgr5high cells are not emerging. Furthermore, relative to CBCs, Msi1+ cells preferentially produce Paneth cells during homeostasis and upon radiation repair. Together, we demonstrate that the DNA damage-resistant Msi1+ cells are cycling ISCs that maintain and regenerate the intestinal epithelium.

Keywords: DNA damage response; Msi1; epithelial regeneration; intestinal stem cells.

Publication types

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

MeSH terms

  • Animals
  • Cell Lineage / genetics
  • Female
  • Homeostasis
  • Intestinal Mucosa / metabolism*
  • Intestinal Mucosa / radiation effects
  • Intestines / physiology*
  • Intestines / radiation effects
  • Male
  • Mice
  • Nerve Tissue Proteins / metabolism
  • Nerve Tissue Proteins / physiology
  • Paneth Cells / metabolism
  • RNA-Binding Proteins / metabolism
  • RNA-Binding Proteins / physiology
  • Radiation Tolerance
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Regeneration / genetics
  • Sequence Analysis, RNA / methods
  • Single-Cell Analysis / methods
  • Stem Cells / metabolism*


  • Lgr5 protein, mouse
  • Msi1h protein, mouse
  • Nerve Tissue Proteins
  • RNA-Binding Proteins
  • Receptors, G-Protein-Coupled