Airway epithelial homeostasis and planar cell polarity signaling depend on multiciliated cell differentiation

被引:63
|
作者
Vladar, Eszter K. [1 ]
Nayak, Jayakar V. [2 ]
Milla, Carlos E. [3 ]
Axelrod, Jeffrey D. [1 ]
机构
[1] Stanford Univ, Dept Pathol, Sch Med, 300 Pasteur Dr,R226a Edwards Bldg, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Pediat, Sch Med, Div Pulm Med, Stanford, CA 94305 USA
来源
JCI INSIGHT | 2016年 / 1卷 / 13期
关键词
CYSTIC-FIBROSIS; CILIA; LUNG; CILIOGENESIS; MORPHOGENESIS; EXPRESSION; VANGL2; AMPLIFICATION; INFLAMMATION; ANGIOGENESIS;
D O I
10.1172/jci.insight.88027
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Motile airway cilia that propel contaminants out of the lung are oriented in a common direction by planar cell polarity (PCP) signaling, which localizes PCP protein complexes to opposite cell sides throughout the epithelium to orient cytoskeletal remodeling. In airway epithelia, PCP is determined in a 2-phase process. First, cell-cell communication via PCP complexes polarizes all cells with respect to the proximal-distal tissue axis. Second, during ciliogenesis, multiciliated cells (MCCs) undergo cytoskeletal remodeling to orient their cilia in the proximal direction. The second phase not only directs cilium polarization, but also consolidates polarization across the epithelium. Here, we demonstrate that in airway epithelia, PCP depends on MCC differentiation. PCP mutant epithelia have misaligned cilia, and also display defective barrier function and regeneration, indicating that PCP regulates multiple aspects of airway epithelial homeostasis. In humans, MCCs are often sparse in chronic inflammatory diseases, and these airways exhibit PCP dysfunction. The presence of insufficient MCCs impairs mucociliary clearance in part by disrupting PCP-driven polarization of the epithelium. Consistent with defective PCP, barrier function and regeneration are also disrupted. Pharmacological stimulation of MCC differentiation restores PCP and reverses these defects, suggesting its potential for broad therapeutic benefit in chronic inflammatory disease.
引用
收藏
页数:18
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