Institute of Laboratory Animal Sciences, Chinese Academy of Medical Sciences, Ministry of Health, Beijing, China.
Comparative Medical Center, Peking Union Medical College, Ministry of Health, Beijing, China.
FASEB J. 2020 Apr;34(4):4918-4933. doi: 10.1096/fj.201902075R. Epub 2020 Feb 18.
Embryonic development of the alveolar sac of the lung is dependent upon multiple signaling pathways to coordinate cell growth, migration, and the formation of the extracellular matrix. Here, we identify GORAB as a regulator of embryonic alveolar sac formation as genetically disrupting the Gorab gene in mice resulted in fatal saccular maturation defects characterized by a thickened lung mesenchyme. This abnormality is not associated with impairments in cellular proliferation and death, but aberrantly increased protein kinase B (AKT) phosphorylation, elevated Vcan transcription, and enhanced migration of mesenchymal fibroblasts. Genetically augmenting PDGFRα, a potent activator of AKT in lung mesenchymal cells, recapitulated the alveolar phenotypes, whereas disrupting PDGFRα partially rescued alveolar phenotypes in Gorab-deficient mice. Overexpressing or suppressing Vcan in primary embryonic lung fibroblasts could, respectively, mimic or attenuate alveolar sac-like phenotypes in a co-culture model. These findings suggest a role of GORAB in negatively regulating AKT phosphorylation, the expression of Vcan, and the migration of lung mesenchyme fibroblasts, and suggest that alveolar sac formation resembles a patterning event that is orchestrated by molecular signaling and the extracellular matrix in the mesenchyme.
肺肺泡囊的胚胎发育依赖于多种信号通路来协调细胞生长、迁移和细胞外基质的形成。在这里,我们确定 GORAB 是胚胎肺泡囊形成的调节剂,因为在小鼠中遗传破坏 Gorab 基因会导致致命的囊泡成熟缺陷,其特征是肺间质增厚。这种异常与细胞增殖和死亡的损伤无关,但异常增加蛋白激酶 B(AKT)磷酸化、Vcan 转录升高和间充质成纤维细胞迁移增强。在肺间质细胞中,遗传增强 PDGFRα(AKT 的有效激活剂)可重现肺泡表型,而在 Gorab 缺陷型小鼠中破坏 PDGFRα 可部分挽救肺泡表型。在原代胚胎肺成纤维细胞中过表达或抑制 Vcan ,可分别在共培养模型中模拟或减弱肺泡囊样表型。这些发现表明 GORAB 在负调控 AKT 磷酸化、Vcan 的表达和肺间质成纤维细胞的迁移中起作用,并表明肺泡囊形成类似于由分子信号和间质中的细胞外基质协调的模式事件。