Chronic lung allograft rejection and airway microvasculature: Is HIF-1 the missing link?

被引:17
|
作者
Wilkes, David S. [1 ,2 ,3 ]
机构
[1] Indiana Univ Sch Med, Ctr Immunobiol, Dept Med, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Ctr Immunobiol, Dept Microbiol, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Ctr Immunobiol, Dept Immunol, Indianapolis, IN 46202 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2011年 / 121卷 / 06期
关键词
OBLITERATIVE BRONCHIOLITIS; TRANSPLANTATION; HYPOXIA; TRANSITION; FIBROSIS; CELLS;
D O I
10.1172/JCI58329
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
Chronic lung allograft rejection, known as obliterative bronchiolitis (OB), is the leading cause of death in lung transplant patients. Although OB pathogenesis is not fully understood, in this issue of the JCI, Jiang and colleagues report that tissue hypoxia resulting in dysfunctional airway microvasculature precedes the airway fibrosis characteristic of OB. In addition, a relative deficiency of allograft endothelial cell-derived HIF-1 alpha contributes to this process. Data showing that overexpressing HIF-1 alpha restores the microvascular airway normoxia and prevents airway fibrosis highlight a novel role for vascular biology in OB pathogenesis.
引用
收藏
页码:2155 / 2157
页数:3
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