Heme oxygenase-1 protects against vascular constriction and proliferation

被引:0
|
作者
Henricus J. Duckers
Manfred Boehm
Andrea L. True
Shaw-Fang Yet
Hong San
James L. Park
R. Clinton Webb
Mu-En Lee
Gary J. Nabel
Elizabeth G. Nabel
机构
[1] Vascular Biology Branch,Department of Physiology
[2] National Heart,Cardiovascular Division
[3] Lung,undefined
[4] and Blood Institute,undefined
[5] Vaccine Research Center,undefined
[6] National Institutes of Health,undefined
[7] Medical College of Georgia,undefined
[8] Brigham and Women's Hospital,undefined
[9] Harvard Medical School,undefined
来源
Nature Medicine | 2001年 / 7卷
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摘要
Heme oxygenase (HO-1, encoded by Hmox1) is an inducible protein activated in systemic inflammatory conditions by oxidant stress. Vascular injury is characterized by a local reparative process with inflammatory components, indicating a potential protective role for HO-1 in arterial wound repair. Here we report that HO-1 directly reduces vasoconstriction and inhibits cell proliferation during vascular injury. Expression of HO-1 in arteries stimulated vascular relaxation, mediated by guanylate cyclase and cGMP, independent of nitric oxide. The unexpected effects of HO-1 on vascular smooth muscle cell growth were mediated by cell-cycle arrest involving p21Cip1. HO-1 reduced the proliferative response to vascular injury in vivo; expression of HO-1 in pig arteries inhibited lesion formation and Hmox1−/− mice produced hyperplastic arteries compared with controls. Induction of the HO-1 pathway moderates the severity of vascular injury by at least two adaptive mechanisms independent of nitric oxide, and is a potential therapeutic target for diseases of the vasculature.
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页码:693 / 698
页数:5
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