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-结晶/ Hspb5通过增强NF-κB诱导的粘附分子ICAM-1,VCAM-1和E-SELETIN的诱导NF-κB诱导的上调诱导内皮 - 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-结晶是一种小的热休克蛋白,通过增加内皮细胞的存活和血管内皮生长因子A的分泌具有促血管生成特性。在这里,我们通过增强肿瘤坏死,证明了αb结晶素在调节血管功能方面的额外作用因子α(TNF-α)诱导白细胞募集中涉及内皮粘附分子的表达。内皮细胞中αB-结晶素的异位表达增加了响应于TNF-α的E-SELECTIN表达水平,并增强体外白细胞 - 内皮相互作用。相反,在从αB晶体缺陷小鼠分离的内皮细胞中显着抑制TNF-α诱导的细胞间粘附分子1,血管细胞粘附分子1和E-SELIEN的表达。这与αB结晶缺陷细胞中的IκB水平升高,并且在TNF-α刺激时不完全降解。符合此,在αB晶体缺陷小鼠的发炎血管中,内皮粘附分子表达减少,并且白细胞轧制速度增加。我们的数据通过增强内皮活化期间的促炎核因子κB信号和内皮粘附分子表达,鉴定αb-crystallin作为白细胞募集的新调节剂。

著录项

  • 来源
    《Angiogenesis》 |2013年第4期|共9页
  • 作者单位

    Rudbeck Laboratory Department of Immunology Genetics and Pathology Uppsala University 751 85;

    Rudbeck Laboratory Department of Immunology Genetics and Pathology Uppsala University 751 85;

    Department of Medical Cell Biology Uppsala University 751 23 Uppsala Sweden;

    Institute of Anatomy and Cell Biology University of Ulm Albert-Einstein-Allee 11 89081 Ulm;

    Department of Medical Cell Biology Uppsala University 751 23 Uppsala Sweden;

    Rudbeck Laboratory Department of Immunology Genetics and Pathology Uppsala University 751 85;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 心脏、血管(循环系)疾病;
  • 关键词

    αB-crystallin; Chaperone; E-selectin; ICAM-1; NF-κB; VCAM-1;

    机译:αB-结晶;伴侣;e-Selectin;ICAM-1;NF-κB;VCAM-1;

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