蛋白质水解
抗原
抗原呈递
细胞生物学
蛋白酵素
生物
抗原提呈细胞
溶酶体
抗原处理
免疫系统
化学
免疫学
生物化学
T细胞
酶
作者
Lélia Delamarre,Margit Pack,Henry Chang,Ira Mellman,E. Sergio Trombetta
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2005-03-11
卷期号:307 (5715): 1630-1634
被引量:714
标识
DOI:10.1126/science.1108003
摘要
Antigen-presenting cells (APCs) internalize antigens and present antigen-derived peptides to T cells. Although APCs have been thought to exhibit a well-developed capacity for lysosomal proteolysis, here we found that they can exhibit two distinct strategies upon antigen encounter. Whereas macrophages contained high levels of lysosomal proteases and rapidly degraded internalized proteins, dendritic cells (DCs) and B lymphocytes were protease-poor, resulting in a limited capacity for lysosomal degradation. Consistent with these findings, DCs in vivo degraded internalized antigens slowly and thus retained antigen in lymphoid organs for extended periods. Limited lysosomal proteolysis also favored antigen presentation. These results help explain why DCs are able to efficiently accumulate, process, and disseminate antigens and microbes systemically for purposes of tolerance and immunity.
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