In toto imaging of early enteric nervous system development reveals that gut colonization is tied to proliferation downstream of Ret

Development. 2022 Nov 1;149(21):dev200668. doi: 10.1242/dev.200668. Epub 2022 Oct 31.

Abstract

The enteric nervous system is a vast intrinsic network of neurons and glia within the gastrointestinal tract and is largely derived from enteric neural crest cells (ENCCs) that emigrate into the gut during vertebrate embryonic development. Study of ENCC migration dynamics and their genetic regulators provides great insights into fundamentals of collective cell migration and nervous system formation, and these are pertinent subjects for study due to their relevance to the human congenital disease Hirschsprung disease (HSCR). For the first time, we performed in toto gut imaging and single-cell generation tracing of ENCC migration in wild type and a novel ret heterozygous background zebrafish (retwmr1/+) to gain insight into ENCC dynamics in vivo. We observed that retwmr1/+ zebrafish produced fewer ENCCs localized along the gut, and these ENCCs failed to reach the hindgut, resulting in HSCR-like phenotypes. Specifically, we observed a proliferation-dependent migration mechanism, where cell divisions were associated with inter-cell distances and migration speed. Lastly, we detected a premature neuronal differentiation gene expression signature in retwmr1/+ ENCCs. These results suggest that Ret signaling may regulate maintenance of a stem state in ENCCs.

Keywords: Differentiation; Enteric nervous system; Enteric neural crest; Proliferation; Ret; Zebrafish.

Publication types

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

MeSH terms

  • Animals
  • Cell Division
  • Cell Movement / genetics
  • Cell Proliferation
  • Enteric Nervous System*
  • Hirschsprung Disease* / genetics
  • Hirschsprung Disease* / metabolism
  • Humans
  • Intestines
  • Neural Crest
  • Proto-Oncogene Proteins c-ret / genetics
  • Proto-Oncogene Proteins c-ret / metabolism
  • Zebrafish / genetics

Substances

  • Proto-Oncogene Proteins c-ret
  • RET protein, human