Thomas Sunil, Kumar Rajeev S, Brumeanu Teodor-D
Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029, USA.
Arch Immunol Ther Exp (Warsz). 2004 Jul-Aug;52(4):215-24.
The plasma membrane of T cells is made up of a combination of phospholipids and proteins organized as glycolipoprotein microdomains termed lipid rafts. The structural assembly of lipid rafts was investigated by various physical and biochemical assays. Depending on the differentiation status of T cells, the lipid rafts seclude various protein receptors instrumental for the early T cell signaling, cytoskeleton reorganization, protein and membrane trafficking, and the entry of infectious organisms into the cells. This review article summarizes recent information on the assembly of lipid rafts in plasma membrane of T cells and their signaling output in mature and thymic precursors towards cell growth and differentiation, and possible modalities by which the function of lipid rafts can be altered by drugs and T cell ligands. The concept of using lipid rafts as a target for pharmaceutical compounds and biological T cell ligands to ultimately alter the T cell function is discussed.
T 细胞的质膜由磷脂和蛋白质组合而成,这些成分组织成称为脂筏的糖脂蛋白微结构域。通过各种物理和生化分析方法对脂筏的结构组装进行了研究。根据 T 细胞的分化状态,脂筏隔离了各种对早期 T 细胞信号传导、细胞骨架重组、蛋白质和膜运输以及感染性生物体进入细胞起重要作用的蛋白质受体。这篇综述文章总结了关于 T 细胞质膜中脂筏组装及其在成熟 T 细胞和胸腺前体细胞中对细胞生长和分化的信号输出的最新信息,以及药物和 T 细胞配体改变脂筏功能的可能方式。文中还讨论了将脂筏作为药物化合物和生物 T 细胞配体的靶点以最终改变 T 细胞功能的概念。