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内皮细胞血管内皮钙黏蛋白作为纤维蛋白β15 - 42序列的受体发挥作用。

Endothelial cell VE-cadherin functions as a receptor for the beta15-42 sequence of fibrin.

作者信息

Bach T L, Barsigian C, Yaen C H, Martinez J

机构信息

Cardeza Foundation for Hematologic Research and Division of Hematology, Department of Medicine, Jefferson Medical College of Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

J Biol Chem. 1998 Nov 13;273(46):30719-28. doi: 10.1074/jbc.273.46.30719.

Abstract

The contact of fibrin with the apical surface of human umbilical vein endothelial cells (HUVEC) can induce capillary tube formation via the interaction of fibrin beta15-42 with a putative cell receptor (Chalupowicz, D. G., Chowdhury, Z. A., Bach, T. L., Barsigian, C., and Martinez, J. (1995) J. Cell Biol. 130, 207-215). To characterize this interaction, we studied the binding of the thrombin-cleaved N-terminal disulfide knot of fibrin (NDSK II), a dimeric fragment with exposed beta15-42, to HUVEC in three separate assay systems. Time-course binding of 125I-NDSK II to HUVEC monolayers or suspensions revealed that binding was specific at 50-60%, as determined by the addition of unlabeled NDSK II. Specific binding of 125I-NDSK II to HUVEC was 70% reversible by dilution or by competition, and was found to be divalent cation-independent. Binding plateaued after 10 min at a saturation of 15-20 nM. Scatchard analysis using the LIGAND computer program defined a single population of receptors with a KD of 7.7 +/- 1.6 nM and approximately 21,000 +/- 7000 binding sites/cell. N-terminal disulfide knot derivatives in which beta15-42 was absent (NDSK 325) or unexposed (NDSK, NDSK I) did not show specific binding. Specific binding of 125I-NDSK II could not be inhibited by RGDS or by antibodies to the alphavbeta3 or beta1 integrins, PECAM-1, ICAM-1, or N-cadherin. In contrast, a synthetic beta15-42/ovalbumin conjugate inhibited total 125I-NDSK II binding by 47 +/- 19% (corresponding to 95% of specific 125I-NDSK II bound) and a monoclonal antibody to vascular endothelial cadherin (VE-cadherin) inhibited binding by 35 +/- 8% (corresponding to 70% of specific 125I-NDSK II bound). Another assay was based on the capture of cadherins from HUVEC lysates by a polyclonal pan-cadherin antibody immobilized on plastic dishes. Binding of NDSK II to the captured cadherins was 89 +/- 5% specific, while specific binding of NDSK 325 and NDSK was negligible. An immortalized line of human adipose-derived microvascular endothelial cells, which express N-cadherin but not VE-cadherin, demonstrated no specific binding of NDSK II by the capture assay. These data define a novel interaction of fibrin with VE-cadherin, which is mediated by the fibrin N-terminal beta15-42 sequence, and may contribute to the mechanism through which fibrin induces angiogenesis.

摘要

纤维蛋白与人脐静脉内皮细胞(HUVEC)顶端表面的接触可通过纤维蛋白β15 - 42与一种假定的细胞受体的相互作用诱导毛细血管管形成(Chalupowicz, D. G., Chowdhury, Z. A., Bach, T. L., Barsigian, C., and Martinez, J. (1995) J. Cell Biol. 130, 207 - 215)。为了表征这种相互作用,我们在三个独立的检测系统中研究了纤维蛋白经凝血酶切割的N端二硫键结(NDSK II)(一种具有暴露的β15 - 42的二聚体片段)与HUVEC的结合。125I - NDSK II与HUVEC单层或悬浮液的时间进程结合显示,如通过添加未标记的NDSK II所确定的,结合特异性为50 - 60%。125I - NDSK II与HUVEC的特异性结合通过稀释或竞争有70%可逆,并且发现其不依赖二价阳离子。10分钟后结合达到平台期,饱和度为15 - 20 nM。使用LIGAND计算机程序进行的Scatchard分析确定了单一群体的受体,其解离常数(KD)为7.7±1.6 nM,每个细胞约有21,000±7000个结合位点。不存在β15 - 42(NDSK 325)或未暴露β15 - 42(NDSK、NDSK I)的N端二硫键结衍生物未显示出特异性结合。125I - NDSK II的特异性结合不能被RGDS或抗αvβ3或β1整合素、PECAM - 1、ICAM - 1或N - 钙黏蛋白的抗体抑制。相反,一种合成的β15 - 42/卵清蛋白偶联物抑制了125I - NDSK II的总结合47±19%(相当于结合的特异性125I - NDSK II的95%),并且一种抗血管内皮钙黏蛋白(VE - cadherin)的单克隆抗体抑制结合35±8%(相当于结合的特异性125I - NDSK II的70%)。另一种检测基于通过固定在塑料培养皿上的多克隆泛钙黏蛋白抗体从HUVEC裂解物中捕获钙黏蛋白。NDSK II与捕获的钙黏蛋白的结合特异性为89±5%,而NDSK 325和NDSK的特异性结合可忽略不计。一种表达N - 钙黏蛋白但不表达VE - 钙黏蛋白的人脂肪来源的微血管内皮细胞永生化细胞系,通过捕获检测未显示NDSK II的特异性结合。这些数据确定了纤维蛋白与VE - 钙黏蛋白之间的一种新型相互作用,其由纤维蛋白N端β15 - 42序列介导,并且可能有助于纤维蛋白诱导血管生成的机制。

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