Turner M L
Department of Haematology, Royal Infirmary of Edinburgh.
Biol Rev Camb Philos Soc. 1992 Aug;67(3):359-77. doi: 10.1111/j.1469-185x.1992.tb00729.x.
Cell adhesion molecules are pivotal to the development and maintenance of tissue structure in metazoan organisms. In mammals, several families of proteins are involved in cell-cell and cell-matrix adhesion. The cadherins are homophilic, primary CAMs, involved in the establishment of boundaries between cell collectives early in embryogenesis. The Ig gene superfamily have diversified widely, with homophilic and heterophilic CAMs and antigen recognition molecules amongst the members. The Integrin family play an important role in binding to extracellular matrix, as well as counter-receptors on the surface of other cells. The Selectin family and HCAM are carbohydrate-binding proteins, and play a prominent role in the circulation of lymphocytes and neoplastic cells. CAMs are fundamental to development of tissue structure in metazoan organisms. Cellular differentiation dictates adherence to a specific microenvironment, through the pattern of surface CAM expression. Conversely, CAM binding can affect gene expression within the cell itself. Cell differentiation and cell adhesion are interdependent processes. In the adult, CAM are crucial to tissue maintenance. Cells frequently change their adhesive properties in response to physiological or pathological processes. The integrity of the vascular system is maintained by circulating platelets which are capable of rapid upregulation of cell adhesion and profound changes in metabolism, on contact with subendothelial matrix. Both endothelial cells and neutrophils undergo changes in CAM expression in response to inflammatory mediators, permitting rapid and appropriate recruitment of phagocytes to damaged tissue. Tissue repair is dependent on phenotypic changes in normally static cells, allowing increased motility and replication. The immune system requires constitutive cells to undergo multiple complex adhesion and detachment events over short periods of time, and is capable of discriminating normal self from aberrant-self or non-self, through antigen specific recognition and adhesion molecules. The pathophysiology of processes such as infection and neoplasia are profoundly affected by cellular CAM expression. CAMs and related molecules are fundamental to the development, maintenance and surveillance of tissue structure.
细胞黏附分子对于后生动物组织结构的发育和维持至关重要。在哺乳动物中,有几个蛋白质家族参与细胞间和细胞与基质的黏附。钙黏着蛋白是同源性的主要细胞黏附分子,在胚胎发育早期参与细胞群体之间边界的建立。免疫球蛋白基因超家族种类繁多,其成员包括同源性和异源性细胞黏附分子以及抗原识别分子。整合素家族在与细胞外基质以及其他细胞表面的反受体结合中发挥重要作用。选择素家族和血细胞黏附分子是碳水化合物结合蛋白,在淋巴细胞和肿瘤细胞的循环中起重要作用。细胞黏附分子是后生动物组织结构发育的基础。细胞分化通过表面细胞黏附分子的表达模式决定细胞对特定微环境的黏附。相反,细胞黏附分子的结合可以影响细胞自身的基因表达。细胞分化和细胞黏附是相互依存的过程。在成体中,细胞黏附分子对于组织维持至关重要。细胞经常根据生理或病理过程改变其黏附特性。血管系统的完整性由循环血小板维持,血小板在与内皮下基质接触时能够迅速上调细胞黏附并发生代谢的深刻变化。内皮细胞和中性粒细胞都会因炎症介质而发生细胞黏附分子表达的变化,从而使吞噬细胞能够迅速且适当地募集到受损组织。组织修复依赖于正常静止细胞的表型变化,使其运动性和复制能力增强。免疫系统要求组成细胞在短时间内经历多次复杂的黏附和解离事件,并且能够通过抗原特异性识别和黏附分子区分正常自身与异常自身或非自身。感染和肿瘤形成等过程的病理生理学受到细胞细胞黏附分子表达的深刻影响。细胞黏附分子及相关分子对于组织结构的发育、维持和监测至关重要。