Cairo Christopher W, Golan David E
Department of Chemistry, Alberta Ingenuity Centre for Carbohydrate Science, University of Alberta, Edmonton, Alberta, Canada T6G 2G2.
Biopolymers. 2008 May;89(5):409-19. doi: 10.1002/bip.20898.
Cell surface receptors mediate the exchange of information between cells and their environment. In the case of adhesion receptors, the spatial distribution and molecular associations of the receptors are critical to their function. Therefore, understanding the mechanisms regulating the distribution and binding associations of these molecules is necessary to understand their functional regulation. Experiments characterizing the lateral mobility of adhesion receptors have revealed a set of common mechanisms that control receptor function and thus cellular behavior. The T cell provides one of the most dynamic examples of cellular adhesion. An individual T cell makes innumerable intercellular contacts with antigen presenting cells, the vascular endothelium, and many other cell types. We review here the mechanisms that regulate T cell adhesion receptor lateral mobility as a window into the molecular regulation of these systems, and we present a general framework for understanding the principles and mechanisms that are likely to be common among these and other cellular adhesion systems. We suggest that receptor lateral mobility is regulated via four major mechanisms-reorganization, recruitment, dispersion, and anchoring-and we review specific examples of T cell adhesion receptor systems that utilize one or more of these mechanisms.
细胞表面受体介导细胞与其环境之间的信息交换。就黏附受体而言,受体的空间分布和分子关联对其功能至关重要。因此,了解调节这些分子分布和结合关联的机制对于理解其功能调节是必要的。表征黏附受体侧向移动性的实验揭示了一组控制受体功能从而控制细胞行为的共同机制。T细胞提供了细胞黏附最具动态性的例子之一。单个T细胞与抗原呈递细胞、血管内皮以及许多其他细胞类型进行无数次细胞间接触。我们在此回顾调节T细胞黏附受体侧向移动性的机制,以此作为了解这些系统分子调节的窗口,并提出一个通用框架,用于理解这些以及其他细胞黏附系统中可能共有的原理和机制。我们认为受体侧向移动性通过四种主要机制进行调节——重组、募集、分散和锚定——并回顾利用这些机制中的一种或多种的T细胞黏附受体系统的具体例子。