KLF5 Shapes Developing Respiratory Tubules by Inhibiting Actin Asymmetry in Epithelial Cells.

IF 5.9 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qing Li, Yong Liao, Junwei Zeng, Silu Hu, Chunjie Li, Jeffrey A Whitsett, Yi Zheng, Fengming Luo, Chang Xu, Taozhen He, Xinhua Lin, Huajing Wan
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引用次数: 0

Abstract

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 Klf5 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 levels were observed in epithelial cells lining dilated tubules in lungs from patients with congenital pulmonary airway malformation (CPAM). Together, our study demonstrates 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.

KLF5 通过抑制上皮细胞中肌动蛋白的不对称性来塑造发育中的呼吸小管
肾小管的生成依赖于由肌动蛋白细胞骨架的不对称张力驱动的精确的细胞形状变化。肌动蛋白的不对称性是如何被动态控制以协调呼吸管生成所需的上皮细胞形状变化的,目前仍是未知数。在这里,我们揭示了转录因子 KLF5 在调节肌动蛋白不对称性方面的关键作用,它通过 RICH2 平衡 RHOA 和 CDC42 GTPase 的活性,诱导上皮细胞形状的改变。肺上皮细胞中条件性 Klf5 表达或缺失会影响顶端肌动蛋白的组织和顶端极性蛋白在细胞膜中的定位,从而在小鼠肺形态发生过程中破坏呼吸小管的分支和囊状结构。在先天性肺气道畸形(CPAM)患者肺部扩张的肺小管内衬上皮细胞中观察到 KLF5 水平升高。总之,我们的研究表明,KLF5对顶端肌动蛋白组织的动态调控对呼吸小管的发生至关重要,为理解呼吸小管的形态发生提供了一个机理框架。
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来源期刊
CiteScore
11.20
自引率
3.10%
发文量
370
审稿时长
3-8 weeks
期刊介绍: The American Journal of Respiratory Cell and Molecular Biology publishes papers that report significant and original observations in the area of pulmonary biology. The focus of the Journal includes, but is not limited to, cellular, biochemical, molecular, developmental, genetic, and immunologic studies of lung cells and molecules.
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