Dasgupta J D, Watkins S, Slayter H, Yunis E J
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
J Immunol. 1988 Oct 15;141(8):2577-80.
The present investigations show that class I HLA are internalized by macrophage/monocyte type cells. Anti-class I antibody-binding assays show that about 30% of class I Ag present on cell surface are endocytosed within 1 h. Electronmicroscopic investigations reveal that, like other well established receptor molecules, internalization of HLA is mediated by coated pits and coated vesicles. The endocytosed Ag are transferred from endosomes to trans-Golgi reticulum and trans-Golgi cisternae, suggesting recycling of these Ag back to the cell surface. In the presence of phorbol ester tetradecanoyl phorbol acetate, there is a modest increase in the rate of internalization. These results are consistent with the hypothesis that class I Ag on monocytes/macrophages behave like receptor molecules. Malignant transformation of monocytic cells apparently causes the loss of this property of class I Ag.
目前的研究表明,I类HLA被巨噬细胞/单核细胞类型的细胞内化。抗I类抗体结合试验表明,细胞表面约30%的I类抗原在1小时内被内吞。电子显微镜研究显示,与其他已明确的受体分子一样,HLA的内化是由被膜小窝和被膜小泡介导的。内吞的抗原从内体转移到反式高尔基体网状结构和反式高尔基体潴泡,提示这些抗原循环回到细胞表面。在佛波酯十四酰佛波醇乙酸酯存在的情况下,内化速率有适度增加。这些结果与单核细胞/巨噬细胞上的I类抗原表现得像受体分子这一假说相一致。单核细胞的恶性转化显然导致I类抗原这一特性的丧失。