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首页> 外文期刊>Angiogenesis >αb-crystallin/HspB5 regulates endothelial-leukocyte interactions by enhancing NF-κB-induced up-regulation of adhesion molecules ICAM-1, VCAM-1 and E-selectin
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αb-crystallin/HspB5 regulates endothelial-leukocyte interactions by enhancing NF-κB-induced up-regulation of adhesion molecules ICAM-1, VCAM-1 and E-selectin

机译:αb-crystallin/ HspB5通过增强NF-κB诱导的粘附分子ICAM-1,VCAM-1和E-选择素的上调来调节内皮-白细胞相互作用

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摘要

αB-crystallin is a small heat shock protein, which has pro-angiogenic properties by increasing survival of endothelial cells and secretion of vascular endothelial growth factor A. Here we demonstrate an additional role of αB-crystallin in regulating vascular function, through enhancing tumor necrosis factor α (TNF-α) induced expression of endothelial adhesion molecules involved in leukocyte recruitment. Ectopic expression of αB-crystallin in endothelial cells increases the level of E-selectin expression in response to TNF-α, and enhances leukocyte-endothelial interaction in vitro. Conversely, TNF-α-induced expression of intercellular adhesion molecule 1, vascular cell adhesion molecule 1 and E-selectin is markedly inhibited in endothelial cells isolated from αB-crystallin-deficient mice. This is associated with elevated levels of IκB in αB-crystallin deficient cells and incomplete degradation upon TNF-α stimulation. Consistent with this, endothelial adhesion molecule expression is reduced in inflamed vessels of αB-crystallin deficient mice, and leukocyte rolling velocity is increased. Our data identify αB-crystallin as a new regulator of leukocyte recruitment, by enhancing pro-inflammatory nuclear factor κ B-signaling and endothelial adhesion molecule expression during endothelial activation.
机译:αB-crystallin是一种小的热休克蛋白,通过增加内皮细胞的存活率和分泌血管内皮生长因子A而具有促血管生成特性。在这里,我们证明了αB-crystallin通过增强肿瘤坏死调节血管功能的其他作用。因子α(TNF-α)诱导参与白细胞募集的内皮粘附分子表达。内皮细胞中αB-晶状蛋白的异位表达增加了对TNF-α响应的E-选择素表达水平,并增强了体外白细胞-内皮相互作用。相反,TNF-α诱导的细胞间粘附分子1,血管细胞粘附分子1和E-选择蛋白的表达在从缺乏αB-晶状体蛋白的小鼠分离的内皮细胞中受到明显抑制。这与αB-晶状体蛋白缺陷细胞中IκB水平升高和TNF-α刺激后降解不完全有关。与此相一致,在αB-晶状体蛋白缺乏的小鼠的发炎的血管中内皮粘附分子的表达降低,并且白细胞滚动速度增加。我们的数据通过在内皮细胞激活过程中增强促炎性核因子κB信号和内皮粘附分子的表达,从而确定αB-晶状体蛋白是白细胞募集的新调节剂。

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