Anderson H A, Hiltbold E M, Roche P A
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Nat Immunol. 2000 Aug;1(2):156-62. doi: 10.1038/77842.
The plasma membranes of eukaryotic cells are not uniform and possess distinct cholesterol- and sphingolipid-rich raft microdomains that are enriched in proteins known to be essential for cellular function. Lipid raft microdomains are important for T cell receptor (TCR)-mediated activation of T cells. However, the importance of lipid rafts on antigen presenting cells (APCs) and their role in major histocompatibility (MHC) class II-restricted antigen presentation has not been examined. MHC class II molecules were found to be constitutively present in plasma membrane lipid rafts in B cells. Disruption of these microdomains dramatically inhibited antigen presentation at limiting concentrations of antigen. The inhibitory effect of raft disruption on antigen presentation could be overcome by loading the APCs with exceptionally high doses of antigen, showing that raft association concentrates MHC class II molecules into microdomains that allow efficient antigen presentation at low ligand densities.
真核细胞的质膜并非均匀一致,而是拥有独特的富含胆固醇和鞘脂的脂筏微结构域,这些微结构域富含对细胞功能至关重要的蛋白质。脂筏微结构域对于T细胞受体(TCR)介导的T细胞活化很重要。然而,脂筏在抗原呈递细胞(APC)上的重要性及其在主要组织相容性复合体(MHC)II类限制性抗原呈递中的作用尚未得到研究。发现MHC II类分子在B细胞质膜脂筏中组成性存在。这些微结构域的破坏在抗原浓度有限时显著抑制抗原呈递。通过用极高剂量的抗原加载APC,可以克服脂筏破坏对抗原呈递的抑制作用,这表明脂筏关联将MHC II类分子浓缩到微结构域中,从而在低配体密度下实现高效的抗原呈递。