Mesenchymal GDNF promotes intestinal enterochromaffin cell differentiation

Enteroendocrine cells (EECs) differentiate and mature to form functionally distinct populations upon migration along the intestinal crypt-villus axis, but how niche signals affect this process is poorly understood. Here, we identify expression of Glial cell line-derived neurotrophic factor (GDNF) in the intestinal subepithelial myofibroblasts (SEMFs), while the GDNF receptor RET was expressed in a subset of EECs, suggesting GDNF-mediated regulation. Indeed, GDNF-RET signaling induced increased expression of EEC genes including <i>Tph1</i>, encoding for the rate-limiting enzyme for 5-hydroxytryptamine (5-HT, serotonin) biosynthesis, and increased the frequency of 5-HT+ enterochromaffin cells (ECs) in mouse organoid culture experiments and <i>in vivo</i>. Moreover, expression of the 5-HT receptor <i>Htr4</i> was enriched in Lgr5+ intestinal stem cells (ISCs) and 5-HT reduced the ISC clonogenicity. In summary, our results show that GDNF-RET signaling regulate EEC differentiation, and suggest 5-HT as a potential niche factor regulating Lgr5+ ISC activity, with potential implications in intestinal regeneration.

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Publication Details

Journal
iScience
Published
2024-10-24
DOI
https://doi.org/10.1016/j.isci.2024.111246
Citations
1
Primary Topic
Congenital gastrointestinal and neural anomalies
Type
article
Field-Weighted Citation Impact
0.57

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article

Mesenchymal GDNF promotes intestinal enterochromaffin cell differentiation

Pekka Katajisto, Linnea Wartiovaara, Tomi P. Mäkelä, Toni T Lemmetyinen et al.
1 citations
iScience
Congenital gastrointestinal and neural anomalies
0.57
article

Mesenchymal GDNF promotes intestinal enterochromaffin cell differentiation

Pekka Katajisto, Linnea Wartiovaara, Tomi P. Mäkelä, Toni T Lemmetyinen, Saara Ollila, Pekka Päivinen, Nalle Pentinmikko, Heikki Virtanen, Jaan‐Olle Andressoo, Emma W Viitala, Timothy C. Wang
article en
1 citations

Abstract

Enteroendocrine cells (EECs) differentiate and mature to form functionally distinct populations upon migration along the intestinal crypt-villus axis, but how niche signals affect this process is poorly understood. Here, we identify expression of Glial cell line-derived neurotrophic factor (GDNF) in the intestinal subepithelial myofibroblasts (SEMFs), while the GDNF receptor RET was expressed in a subset of EECs, suggesting GDNF-mediated regulation. Indeed, GDNF-RET signaling induced increased expression of EEC genes including <i>Tph1</i>, encoding for the rate-limiting enzyme for 5-hydroxytryptamine (5-HT, serotonin) biosynthesis, and increased the frequency of 5-HT+ enterochromaffin cells (ECs) in mouse organoid culture experiments and <i>in vivo</i>. Moreover, expression of the 5-HT receptor <i>Htr4</i> was enriched in Lgr5+ intestinal stem cells (ISCs) and 5-HT reduced the ISC clonogenicity. In summary, our results show that GDNF-RET signaling regulate EEC differentiation, and suggest 5-HT as a potential niche factor regulating Lgr5+ ISC activity, with potential implications in intestinal regeneration.

iScienceVol. 27(12)
University of Helsinki (FI), Columbia University Irving Medical Center (US), Helsinki Institute of Physics (FI), The Francis Crick Institute (GB), Karolinska Institutet (SE), Helsinki Institute for Information Technology (FI), Cancer Society of Finland (FI)
Academy of Finland, Suomen Kulttuurirahasto, Sigrid Juséliuksen Säätiö, Instrumentariumin Tiedesäätiö
Zero hunger
Openalex Percentile: Top 28%
Congenital gastrointestinal and neural anomalies
0.57
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