细胞迁移
细胞生物学
免疫系统
炎症性肠病
T细胞
炎症
高内皮静脉
运动性
生物
四斯潘宁
免疫学
结肠炎
趋化因子
抗原
整合素
细胞
癌症研究
医学
疾病
病理
遗传学
作者
Einat Zelman-Toister,Eszter Bakos,Sivan Cohen,Ehud Zigmond,Elias Shezen,Valentin Grabovsky,Adi Sagiv,Gili Hart,Nathali Kaushansky,A Ben-Nun,Nitsan Maharshak,Arnoud Sonnenberg,R. Alon,Shirly Becker-Herman,Idit Shachar
标识
DOI:10.1097/mib.0000000000000621
摘要
The continuous recirculation of mature lymphocytes and their entry into the peripheral lymph nodes are crucial for the development of an immune response to foreign antigens. Occasionally, the entry and the subsequent response of T lymphocytes in these sites lead to severe inflammation and pathological conditions. Here, we characterized the tetraspanin molecule, CD151, as a regulator of T cell motility in health and in models of inflammatory bowel disease. CD151 formed a cell surface complex with VLA-4 and LFA-1 integrins, and its activation led to enhanced migration of T cells. Picomolar levels of CCL2 that were previously shown to inhibit T-cell migration to lymph nodes suppressed CD151 expression and dissociated CD151-integrin complexes in T lymphocytes, resulting in attenuated migration toward T-cell attractant chemokines. To directly inhibit CD151 function, a truncated CD151 peptide fragment mimicking of the CD151 extracellular loop was designed. CD151 extracellular loop inhibited T-cell migration in vitro and in vivo and attenuated the development of dextrane sulfate sodium-induced colitis. Thus, CD151 is a key orchestrator of T cell motility; interference with its proper function results in attenuated progression of inflammatory bowel disease.
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