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
Translational Cancer Medicine Program, University of Helsinki, 00014 Helsinki, Finland.
HiLIFE-Helsinki Institute of Life Science, University of Helsinki, 00014 Helsinki, Finland.
iScience. 2024 Oct 24;27(12):111246. doi: 10.1016/j.isci.2024.111246. eCollection 2024 Dec 20.
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.
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。