Increased expression of fibronectin and the α5β1 integrin in angiogenic cerebral blood vessels of mice subject to hypobaric hypoxia

被引:94
|
作者
Milner, Richard [1 ]
Hung, Stephanie [1 ]
Erokwu, Bernadette [2 ]
Dore-Duffy, Paula [3 ]
LaManna, Joseph C. [2 ]
del Zoppo, Gregory J. [1 ]
机构
[1] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[2] Case Western Reserve Univ, Sch Med, Dept Anat, Cleveland, OH 44106 USA
[3] Wayne State Sch Med, Dept Neurol, Detroit, MI USA
关键词
CNS; angiogenesis; hypoxia; capillary; extracellular matrix (ECM); fibronectin; alpha; 5; beta; 1; integrin; MECA-32;
D O I
10.1016/j.mcn.2008.01.013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The extracellular matrix (ECM) is an important regulator of angiogenesis and vascular remodeling. We showed previously that angiogenic capillaries in the developing CNS express high levels of fibronectin and its receptor alpha 5 beta 1 integrin, and that this expression is developmentally downregulated. As cerebral hypoxia leads to an angiogenic response, we sought to determine whether angiogenic vessels in the adult CNS re-express fibronectin and the alpha 5 beta 1 integrin. Ten-week old mice were subject to hypobaric hypoxia for 0, 4, 7 and 14 days, and fibronectin/integrin expression examined. Fibronectin and the alpha 5 integrin subunit were strongly upregulated on capillaries in the hypoxic CNS, with the effect maximal at the earliest time point examined (4 days). Immunofluorescent studies demonstrated that the alpha 5 integrin was expressed by angiogenic endothelial cells. In light of the defined angiogenic role for fibronectin in other systems, this work suggests that induction of fibronectin-alpha 5 beta 1 integrin expression may be an important molecular switch driving angiogenesis in the hypoxic CNS. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:43 / 52
页数:10
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