Zhejiang Key Laboratory of Organ Development and Regeneration, Institute of Developmental and Regenerative Biology, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, People's Republic of China.
Zhejiang Key Laboratory of Organ Development and Regeneration, Institute of Developmental and Regenerative Biology, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, People's Republic of China.
J Biol Chem. 2023 Aug;299(8):105034. doi: 10.1016/j.jbc.2023.105034. Epub 2023 Jul 11.
Lung branching morphogenesis relies on a complex coordination of multiple signaling pathways and transcription factors. Here, we found that ablation of the LIM homeodomain transcription factor Islet1 (Isl1) in lung epithelium resulted in defective branching morphogenesis and incomplete formation of five lobes. A reduction in mesenchymal cell proliferation was observed in Isl1 lungs. There was no difference in apoptosis between the wild-type (Shh) and Isl1 embryos. RNA-Seq and in situ hybridization analysis showed that Shh, Ptch1, Sox9, Irx1, Irx2, Tbx2, and Tbx3 were downregulated in the lungs of Isl1 embryos. ChIP assay implied the Shh gene served as a direct target of ISL1, since the transcription factor ISL1 could bind to the Shh epithelial enhancer sequence (MACS1). Also, activation of the Hedgehog pathway via ectopic gene expression rescued the defects caused by Isl1 ablation, confirming the genetic integration of Hedgehog signaling. In conclusion, our works suggest that epithelial Isl1 regulates lung branching morphogenesis through administrating the Shh signaling mediated epithelial-mesenchymal communications.
肺分支形态发生依赖于多种信号通路和转录因子的复杂协调。在这里,我们发现肺上皮细胞中 LIM 同源结构域转录因子 Islet1(Isl1)的缺失导致分支形态发生缺陷和五个叶不完全形成。在 Isl1 肺中观察到间充质细胞增殖减少。野生型(Shh)和 Isl1 胚胎之间的凋亡没有差异。RNA-Seq 和原位杂交分析表明,Shh、Ptch1、Sox9、Irx1、Irx2、Tbx2 和 Tbx3 在 Isl1 胚胎的肺中下调。ChIP 分析表明 Shh 基因是 ISL1 的直接靶标,因为转录因子 ISL1 可以结合 Shh 上皮增强子序列(MACS1)。此外,通过异位基因表达激活 Hedgehog 信号通路可挽救由 Isl1 缺失引起的缺陷,证实 Hedgehog 信号的遗传整合。总之,我们的工作表明上皮细胞 Isl1 通过调节 Shh 信号介导的上皮-间充质通讯来调节肺分支形态发生。