RMA/S CELLS PRESENT ENDOGENOUSLY SYNTHESIZED CYTOSOLIC PROTEINS TO CLASS-I RESTRICTED CYTOTOXIC LYMPHOCYTES-T

被引:136
|
作者
ESQUIVEL, F
YEWDELL, J
BENNINK, J
机构
[1] Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 1992年 / 175卷 / 01期
关键词
D O I
10.1084/jem.175.1.163
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
RMA/S is a mutant cell line with decreased cell surface expression of major histocompatibility complex class I molecules that has been reported to be deficient in presenting endogenously synthesized influenza virus nucleoprotein (NP) to cytotoxic T lymphocytes (CTL). In the present study we show that RMA/S cells can present vesicular stomatitis virus nucleocapsid protein, and, under some conditions, NP, to K(b)- and D(b)-restricted CTL, respectively. Antigen presentation results from processing of cytosolic pools of endogenously synthesized proteins, and not the binding to cell surface class I molecules of antigenic peptides present in the virus inoculum or released from infected cells. Antigen processing of RMA/S differs, however, from processing by wild-type cells in requiring greater amounts of antigen, longer times to assemble or transport class I-peptide complexes, and in being more sensitive to blocking by anti-CD8 antibody. Thus, the antigen processing deficit in RMA/S cells is of a partial rather than absolute nature.
引用
收藏
页码:163 / 168
页数:6
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