ANTIGEN PROCESSING FOR PRESENTATION BY CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX REQUIRES CLEAVAGE BY CATHEPSIN-E

被引:198
作者
BENNETT, K
LEVINE, T
ELLIS, JS
PEANASKY, RJ
SAMLOFF, IM
KAY, J
CHAIN, BM
机构
[1] UCL, DEPT BIOL, MEDAWAR BLDG, GOWER ST, LONDON WC1 6BT, ENGLAND
[2] VET ADM MED CTR, SEPULVEDA, CA 91343 USA
[3] UNIV S DAKOTA, SCH MED, DEPT BIOCHEM & MOLEC BIOL, VERMILLION, SD 57069 USA
[4] UNIV WALES COLL CARDIFF, DEPT BIOCHEM, CARDIFF CF1 1XL, S GLAM, WALES
基金
英国惠康基金;
关键词
D O I
10.1002/eji.1830220626
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Proteolytic degradation (processing) of antigen by antigen-presenting cells is a major regulatory step in the activation of a T lymphocyte immune response. However, the enzymes responsible for antigen processing remain largely undefined. In this study we show that cathepsin E, and not the ubiquitous lysosomal cathepsin D, is the major aspartic proteinase in a murine antigen-presenting cell line, A20. This enzyme is localized to a non-lysosomal compartment of the endosomal system in these cells. Functional studies using a highly specific inhibitor of cathepsin E show that this enzyme is essential for the processing of ovalbumin by this cell line. Thus, cathepsin E, whose function was hitherto unknown, may play a major role in antigen processing.
引用
收藏
页码:1519 / 1524
页数:6
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