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间充质胶质细胞源性神经营养因子促进肠道肠嗜铬细胞分化。

Mesenchymal GDNF promotes intestinal enterochromaffin cell differentiation.

作者信息

Lemmetyinen Toni T, Viitala Emma W, Wartiovaara Linnea, Päivinen Pekka, Virtanen Heikki T, Pentinmikko Nalle, Katajisto Pekka, Mäkelä Tomi P, Wang Timothy C, Andressoo Jaan-Olle, Ollila Saara

机构信息

Translational Cancer Medicine Program, University of Helsinki, 00014 Helsinki, Finland.

HiLIFE-Helsinki Institute of Life Science, University of Helsinki, 00014 Helsinki, Finland.

出版信息

iScience. 2024 Oct 24;27(12):111246. doi: 10.1016/j.isci.2024.111246. eCollection 2024 Dec 20.

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 , 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 . Moreover, expression of the 5-HT receptor 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.

摘要

肠内分泌细胞(EECs)在沿肠隐窝 - 绒毛轴迁移时分化并成熟,形成功能不同的群体,但微环境信号如何影响这一过程却知之甚少。在这里,我们发现神经胶质细胞系源性神经营养因子(GDNF)在肠上皮下肌成纤维细胞(SEMFs)中表达,而GDNF受体RET在一部分EECs中表达,提示存在GDNF介导的调控。事实上,在小鼠类器官培养实验中,GDNF - RET信号传导诱导了包括编码5 - 羟色胺(5 - HT,血清素)生物合成限速酶的基因在内的EEC基因表达增加,并增加了5 - HT⁺肠嗜铬细胞(ECs)的频率。此外,5 - HT受体的表达在Lgr5⁺肠道干细胞(ISCs)中富集,且5 - HT降低了ISC的克隆形成能力。总之,我们的结果表明GDNF - RET信号传导调节EEC分化,并提示5 - HT作为调节Lgr5⁺ ISC活性的潜在微环境因子,对肠道再生具有潜在影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6364/11616604/9588201f033a/fx1.jpg

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