PUBLICATION

Impact of enteric neuronal loss on intestinal cell composition

Authors
Kakiailatu, N.J.M., Zhang, W., Kuil, L.E., Windster, J.D., Bindels, E., Zink, J.T.M., Vermeulen, M., de Graaf, B.M., Sahadew, D., van den Bosch, T.P.P., Huijgen, D., Sloots, C.E.J., Wijnen, R.M.H., Hofstra, R.M.W., de Pater, E., Melotte, V., Alves, M.M.
ID
ZDB-PUB-260501-16
Date
2026
Source
iScience   29: 115491 (Journal)
Registered Authors
Alves, Maria, de Graaf, Bianca, de Pater, Emma, Kakiailatu, Naomi, Kuil, Laura, Windster, Jonathan
Keywords
Integrative aspects of cell biology, Model organism, Transcriptomics
Datasets
GEO:GSE271622, GEO:GSE225510
MeSH Terms
none
PubMed
42063560 Full text @ iScience
Abstract
Hirschsprung disease (HSCR) is a congenital disorder characterized by the absence of an enteric nervous system (ENS) in the distal gut. While the ENS is critical for normal gut function, its broader role in maintaining intestinal homeostasis remains underexplored. Using single-cell RNA sequencing, we investigated the impact of ENS loss on gut composition in wildtype and ret mutant (HSCR model) zebrafish. Significant alterations were identified, including increases in immune cells and shifts in epithelial and extracellular matrix (ECM)-producing cell populations. Immune dysregulation was highlighted by impaired TNF-α signaling via NF-κB, while epithelial changes pointed to disrupted energy homeostasis with downregulated fatty acid metabolism and cell cycle pathways. The ECM-producing cells showed enriched fibrotic markers. Alterations of the intestinal composition were validated in human HSCR tissues, underscoring the clinical relevance of the study. These changes can underlie the development of secondary complications and be potentially used to improve patient outcomes.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping