Li Qing, Liao Yong, Zeng Junwei, Hu Silu, Li Chunjie, Whitsett Jeffrey A, Zheng Yi, Luo Fengming, Xu Chang, He Taozhen, Lin Xinhua, Wan Huajing
State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, China.
State Key Laboratory of Genetic Engineering, School of Life Sciences, Greater Bay Area Institute of Precision Medicine (Guangzhou), Zhongshan Hospital, Fudan University, Shanghai, China.
Am J Respir Cell Mol Biol. 2025 Jun;72(6):663-677. doi: 10.1165/rcmb.2024-0140OC.
Tubulogenesis depends on precise cell shape changes driven by asymmetric tension from the actin cytoskeleton. How actin asymmetry is dynamically controlled to coordinate epithelial cell shape changes required for respiratory tubulogenesis remains unknown. Herein, we unveiled a critical role for the transcription factor KLF5, regulating actin asymmetry, inducing epithelial cell shape changes by balancing RHOA and CDC42 GTPase activity via RICH2. Conditional expression or deletion in pulmonary epithelial cells affected apical actin organization and the positioning of apical polarity proteins in cell membranes, disrupting branching and sacculation of respiratory tubules during mouse lung morphogenesis. Increased KLF5 concentrations were observed in epithelial cells lining dilated tubules in lungs from patients with congenital pulmonary airway malformation. Together, our results demonstrate that dynamic regulation of apical actin organization by KLF5 is essential for respiratory tubulogenesis, providing a mechanistic framework for comprehending the morphogenesis of respiratory tubules.
肾小管发生依赖于由肌动蛋白细胞骨架产生的不对称张力驱动的精确细胞形状变化。肌动蛋白不对称性是如何动态调控以协调呼吸性肾小管发生所需的上皮细胞形状变化仍不清楚。在此,我们揭示了转录因子KLF5的关键作用,其调节肌动蛋白不对称性,通过RICH2平衡RHOA和CDC42 GTP酶活性来诱导上皮细胞形状变化。肺上皮细胞中的条件性表达或缺失影响顶端肌动蛋白组织以及顶端极性蛋白在细胞膜中的定位,破坏小鼠肺形态发生过程中呼吸性小管的分支和囊泡形成。在先天性肺气道畸形患者肺部扩张小管内衬的上皮细胞中观察到KLF5浓度增加。总之,我们的结果表明KLF5对顶端肌动蛋白组织的动态调控对呼吸性肾小管发生至关重要,为理解呼吸性小管的形态发生提供了一个机制框架。