Avian ceca are indispensable for hindgut enteric nervous system development.
Animals
Cell Differentiation
/ genetics
Cell Movement
/ genetics
Chick Embryo
Chickens
/ genetics
Digestive System
/ growth & development
Enteric Nervous System
/ growth & development
Hirschsprung Disease
/ genetics
Humans
Intestines
/ innervation
Neural Crest
/ cytology
Neurons
/ metabolism
RNA
/ genetics
RNA-Seq
Transcriptome
/ genetics
Wnt Proteins
/ genetics
Wnt Signaling Pathway
/ genetics
Ceca
Enteric nervous system
Hindgut
Hirschsprung disease
Neural crest cells
Wnt11
Journal
Development (Cambridge, England)
ISSN: 1477-9129
Titre abrégé: Development
Pays: England
ID NLM: 8701744
Informations de publication
Date de publication:
15 11 2021
15 11 2021
Historique:
received:
25
05
2021
accepted:
22
10
2021
pubmed:
19
11
2021
medline:
12
2
2022
entrez:
18
11
2021
Statut:
ppublish
Résumé
The enteric nervous system (ENS), which is derived from enteric neural crest cells (ENCCs), represents the neuronal innervation of the intestine. Compromised ENCC migration can lead to Hirschsprung disease, which is characterized by an aganglionic distal bowel. During the craniocaudal migration of ENCCs along the gut, we find that their proliferation is greatest as the ENCC wavefront passes through the ceca, a pair of pouches at the midgut-hindgut junction in avian intestine. Removal of the ceca leads to hindgut aganglionosis, suggesting that they are required for ENS development. Comparative transcriptome profiling of the cecal buds compared with the interceca region shows that the non-canonical Wnt signaling pathway is preferentially expressed within the ceca. Specifically, WNT11 is highly expressed, as confirmed by RNA in situ hybridization, leading us to hypothesize that cecal expression of WNT11 is important for ENCC colonization of the hindgut. Organ cultures using embryonic day 6 avian intestine show that WNT11 inhibits enteric neuronal differentiation. These results reveal an essential role for the ceca during hindgut ENS formation and highlight an important function for non-canonical Wnt signaling in regulating ENCC differentiation.
Identifiants
pubmed: 34792104
pii: 273454
doi: 10.1242/dev.199825
pmc: PMC8645208
pii:
doi:
Substances chimiques
Wnt Proteins
0
Wnt11 protein, human
0
RNA
63231-63-0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© 2021. Published by The Company of Biologists Ltd.
Déclaration de conflit d'intérêts
Competing interests The authors declare no competing or financial interests.