首页> 外文期刊>Journal of the American Heart Association Cardiovascular and Cerebrovascular Disease >Tumor Necrosis Factor–Related Apoptosis‐Inducing Ligand (TRAIL) Promotes Angiogenesis and Ischemia‐Induced Neovascularization Via NADPH Oxidase 4 (NOX4) and Nitric Oxide–Dependent Mechanisms
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Tumor Necrosis Factor–Related Apoptosis‐Inducing Ligand (TRAIL) Promotes Angiogenesis and Ischemia‐Induced Neovascularization Via NADPH Oxidase 4 (NOX4) and Nitric Oxide–Dependent Mechanisms

机译:肿瘤坏死因子相关的凋亡诱导配体(TRAIL)通过NADPH氧化酶4(NOX4)和一氧化氮依赖性机制促进血管生成和缺血诱导的新血管形成。

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Background Tumor necrosis factor–related apoptosis‐inducing ligand (TRAIL) has the ability to inhibit angiogenesis by inducing endothelial cell death, as well as being able to promote pro‐angiogenic activity in vitro. These seemingly opposite effects make its role in ischemic disease unclear. Using Trail?/? and wildtype mice, we sought to determine the role of TRAIL in angiogenesis and neovascularization following hindlimb ischemia.
机译:背景肿瘤坏死因子相关的凋亡诱导配体(TRAIL)具有通过诱导内皮细胞死亡来抑制血管生成的能力,并能够在体外促进促血管生成活性。这些看似相反的作用尚不清楚其在缺血性疾病中的作用。使用Trail ?/?和野生型小鼠,我们试图确定TRAIL在后肢缺血后在血管生成和新血管形成中的作用。

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