Exogenous L-arginine increases intestinal stem cell function through CD90+ stromal cells producing mTORC1-induced Wnt2b

Commun Biol. 2020 Oct 23;3(1):611. doi: 10.1038/s42003-020-01347-9.

Abstract

The renewal and repair of intestinal epithelium depend on the self-renewal of intestinal stem cells (ISCs) under physiological and pathological conditions. Although previous work has established that exogenous nutrients regulate adult stem cell activity, little is known about the regulatory effect of L-arginine on ISCs. In this study we utilize mice and small intestinal (SI) organoid models to clarify the role of L-arginine on epithelial differentiation of ISCs. We show that L-arginine increases expansion of ISCs in mice. Furthermore, CD90+ intestinal stromal cells augment stem-cell function in response to L-arginine in co-culture experiments. Mechanistically, we find that L-arginine stimulates Wnt2b secretion by CD90+ stromal cells through the mammalian target of rapamycin complex 1 (mTORC1) and that blocking Wnt2b production prevents L-arginine-induced ISC expansion. Finally, we show that L-arginine treatment protects the gut in response to injury. Our findings highlight an important role for CD90+ stromal cells in L-arginine-stimulated ISC expansion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginine / pharmacology*
  • Cell Differentiation / drug effects
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / drug effects*
  • Intestine, Small / cytology
  • Intestine, Small / drug effects
  • Male
  • Mechanistic Target of Rapamycin Complex 1 / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Organoids / drug effects
  • Organoids / metabolism
  • Stem Cells / drug effects*
  • Stem Cells / metabolism
  • Stromal Cells / drug effects*
  • Stromal Cells / metabolism
  • Thy-1 Antigens / metabolism
  • Wnt Proteins / metabolism

Substances

  • Thy-1 Antigens
  • Wnt Proteins
  • Wnt2b protein, mouse
  • Arginine
  • Mechanistic Target of Rapamycin Complex 1