ISL1 regulates lung branching morphogenesis via Shh signaling pathway
Ruiqi Huang, Chujing Zhang, Yuting Zheng, Wei Zhang, Huarong Huang, Mengsheng Qiu, Jianying Li, Feixue Li
Abstract
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 ShhCre lungs. There was no difference in apoptosis between the wild-type ( Shh Cre ) and Isl1 ShhCre 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 ShhCre 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 that 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.