Lrig1 drives cryptogenesis and restrains proliferation during colon development

Am J Physiol Gastrointest Liver Physiol. 2023 Dec 1;325(6):G570-G581. doi: 10.1152/ajpgi.00094.2023. Epub 2023 Oct 24.

Abstract

Growth and specification of the mouse intestine occurs in utero and concludes after birth. Although numerous studies have examined this developmental process in the small intestine, far less is known about the cellular and molecular cues required for colon development. In this study, we examine the morphological events leading to crypt formation, epithelial cell differentiation, proliferation, and the emergence and expression of a stem and progenitor cell marker Lrig1. Through multicolor lineage tracing, we show Lrig1-expressing cells are present at birth and behave as stem cells to establish clonal crypts within 3 wk of life. In addition, we use an inducible knockout mouse to eliminate Lrig1 and show Lrig1 restrains proliferation within a critical developmental time window, without impacting colonic epithelial cell differentiation. Our study illustrates morphological changes during crypt development and the importance of Lrig1 in the developing colon.NEW & NOTEWORTHY Our studies define the importance of studying Lrig1 in colon development. We address a critical gap in the intestinal development literature and provide new information about the molecular cues that guide colon development. Using a novel, inducible knockout of Lrig1, we show Lrig1 is required for appropriate colon epithelial growth and illustrate the importance of Lrig1-expressing cells in the establishment of colonic crypts.

Keywords: Lrig1; colon; development; stem cells.

Publication types

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

MeSH terms

  • Animals
  • Cell Proliferation
  • Colon / metabolism
  • Colonic Neoplasms* / metabolism
  • Intestinal Mucosa / metabolism
  • Intestine, Small / metabolism
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Knockout
  • Nerve Tissue Proteins* / metabolism

Substances

  • Nerve Tissue Proteins
  • Lrig1 protein, mouse
  • Membrane Glycoproteins