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T细胞整合素受体功能的调控机制。

Regulatory mechanisms underlying T cell integrin receptor function.

作者信息

Mobley J L, Reynolds P J, Shimizu Y

机构信息

Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109.

出版信息

Semin Immunol. 1993 Aug;5(4):227-36. doi: 10.1006/smim.1993.1027.

Abstract

Adhesion molecules allow lymphocytes to interact with and respond to the extracellular environment. Since these interactions must be essentially transient in nature, the function of lymphocyte adhesion molecules must be precisely regulated. Studies of integrin receptors vividly illustrate the various mechanisms by which the function of these adhesion molecules can be regulated. These include: (1) activation-dependent changes in functional activity; (2) changes in levels of expression due to differentiation events; (3) cell-specific differences in integrin binding; and (4) differential binding to distinct ligands by the same integrin. These mechanisms provide highly precise and specific modes of regulating lymphocyte interactions with a wide variety of potential counter-receptors and ligands.

摘要

黏附分子使淋巴细胞能够与细胞外环境相互作用并对其作出反应。由于这些相互作用本质上必然是短暂的,淋巴细胞黏附分子的功能必须受到精确调控。对整合素受体的研究生动地阐明了调控这些黏附分子功能的各种机制。这些机制包括:(1) 功能活性的激活依赖性变化;(2) 由于分化事件导致的表达水平变化;(3) 整合素结合的细胞特异性差异;以及(4) 同一整合素与不同配体的差异性结合。这些机制提供了高度精确和特异的模式,用于调控淋巴细胞与多种潜在的反受体和配体之间的相互作用。

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