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αvβ3整合素在单核细胞迁移中的作用。

A role for the alphavbeta3 integrin in the transmigration of monocytes.

作者信息

Weerasinghe D, McHugh K P, Ross F P, Brown E J, Gisler R H, Imhof B A

机构信息

Basel Institute for Immunology, CH-4005 Basel, Switzerland.

出版信息

J Cell Biol. 1998 Jul 27;142(2):595-607. doi: 10.1083/jcb.142.2.595.

DOI:10.1083/jcb.142.2.595
PMID:9679155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2133044/
Abstract

The beta2 integrins and intercellular adhesion molecule-1 (ICAM-1) are important for monocyte migration through inflammatory endothelium. Here we demonstrate that the integrin alphavbeta3 is also a key player in this process. In an in vitro transendothelial migration assay, monocytes lacking beta3 integrins revealed weak migratory ability, whereas monocytes expressing beta3 integrins engaged in stronger migration. This migration could be partially blocked by antibodies against the integrin chains alphaL, beta2, alphav, or IAP, a protein functionally associated with alphavbeta3 integrin. Transfection of beta3 integrin chain cDNA into monocytes lacking beta3 integrins resulted in expression of the alphavbeta3 integrin and conferred on these cells an enhanced ability to transmigrate through cell monolayers expressing ICAM-1. These monocytes also engaged in alphaLbeta2-dependent locomotion on recombinant ICAM-1 which was enhanced by alphavbeta3 integrin occupancy. Antibodies against IAP were able to revert this alphavbeta3 integrin-dependent cell locomotion to control levels. Finally, adhesion assays revealed that occupancy of alphavbeta3 integrin could decrease monocyte binding to ICAM-1. In conclusion, we show that alphavbeta3 integrin modulates alphaLbeta2 integrin-dependent monocyte adhesion to and migration on ICAM-1. This could represent a novel mechanism to promote monocyte motility on vascular ICAM-1 and initiate subsequent transendothelial migration.

摘要

β2整合素和细胞间黏附分子-1(ICAM-1)对于单核细胞通过炎症内皮的迁移很重要。在此我们证明整合素αvβ3在这一过程中也是关键参与者。在体外跨内皮迁移试验中,缺乏β3整合素的单核细胞显示出较弱的迁移能力,而表达β3整合素的单核细胞迁移能力更强。这种迁移可被针对整合素链αL、β2、αv或IAP(一种与αvβ3整合素功能相关的蛋白质)的抗体部分阻断。将β3整合素链cDNA转染到缺乏β3整合素的单核细胞中,导致αvβ3整合素表达,并赋予这些细胞增强的穿过表达ICAM-1的细胞单层的迁移能力。这些单核细胞在重组ICAM-1上也进行αLβ2依赖性运动,αvβ3整合素占据可增强这种运动。针对IAP的抗体能够将这种αvβ3整合素依赖性细胞运动恢复到对照水平。最后,黏附试验显示αvβ3整合素的占据可减少单核细胞与ICAM-1的结合。总之,我们表明αvβ3整合素调节αLβ2整合素依赖性单核细胞对ICAM-1的黏附和在ICAM-1上的迁移。这可能代表一种促进单核细胞在血管ICAM-1上运动并启动随后跨内皮迁移的新机制。

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