Airway epithelial cell migration and wound repair by ATP-mediated activation of dual oxidase 1

被引:121
|
作者
Wesley, Umadevi V.
Bove, Peter F.
Hristova, Milena
McCarthy, Sean
van der Vliet, Albert
机构
[1] Univ Vermont, Dept Pathol, Burlington, VT 05405 USA
[2] Univ Vermont, Dept Microbiol & Mol Genet, Burlington, VT 05405 USA
关键词
D O I
10.1074/jbc.M606533200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The airway epithelium is continuously subjected to environmental pollutants, airborne pathogens, and allergens and relies on several intrinsic mechanisms to maintain barrier integrity and to promote epithelial repair processes following injury. Here, we report a critical role for dual oxidase 1 (Duox1), a newly identified NADPH oxidase homolog within the tracheobronchial epithelium, in airway epithelial cell migration and repair following injury. Activation of Duox1 during epithelial injury is mediated by cellular release of ATP, which signals through purinergic receptors expressed on the epithelial cell surface. Purinergic receptor stimulation by extracellular ATP is a critical determinant of epithelial cell migration and repair following injury and is associated with activation of extracellular signal-regulated kinases (ERK1/2) and matrix metalloproteinase-9 (MMP-9). Stimulation of these integral features of epithelial cell migration and repair processes was found to require the activation of Duox1. Our findings demonstrate a novel role for Duox1 in the tracheobronchial epithelium, in addition to its proposed role in antimicrobial host defense, by participating in epithelial repair processes to maintain epithelial integrity and barrier function in the face of environmental stress.
引用
收藏
页码:3213 / 3220
页数:8
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