Selective proteasome inhibitors: modulators of antigen presentation?

被引:42
作者
Groettrup, M
Schmidtke, G
机构
[1] Research Department, Cantonal Hospital St. Gall, Bldg 09
关键词
D O I
10.1016/S1359-6446(98)01292-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The proteasome is the main nonlysosomal endoprotease in the cytoplasm and nucleus of all eukaryotic cells. It is responsible for the generation of most antigenic peptides as ligands for major histocompatibility complex (MHC) class I proteins. The proteasome hence qualifies as a target for modifying or silencing antigen processing and presentation to cytotoxic T cells, which are important players in transplant rejection and autoimmune disease. The authors summarize recent progress in the understanding of antigen processing by the proteasome and discuss the potential of novel and selective proteasome inhibitors as drugs for suppressing or modifying the cytotoxic immune response.
引用
收藏
页码:63 / 71
页数:9
相关论文
共 92 条
[1]   Potent and selective inhibitors of the proteasome: Dipeptidyl boronic acids [J].
Adams, J ;
Behnke, M ;
Chen, SW ;
Cruickshank, AA ;
Dick, LR ;
Grenier, L ;
Klunder, JM ;
Ma, YT ;
Plamondon, L ;
Stein, RL .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (04) :333-338
[2]  
AHN JY, 1995, FEBS LETT, V366, P37, DOI 10.1016/0014-5793(95)00492-R
[3]   In vivo characterization of the proteasome regulator PA28 [J].
Ahn, K ;
Erlander, M ;
Leturcq, D ;
Peterson, PA ;
Fruh, K ;
Yang, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) :18237-18242
[4]   CDNA CLONING AND INTERFERON-GAMMA DOWN-REGULATION OF PROTEASOMAL SUBUNIT-X AND SUBUNIT-Y [J].
AKIYAMA, KY ;
YOKOTA, KY ;
KAGAWA, S ;
SHIMBARA, N ;
TAMURA, T ;
AKIOKA, H ;
NOTHWANG, HG ;
NODA, C ;
TANAKA, K ;
ICHIHARA, A .
SCIENCE, 1994, 265 (5176) :1231-1234
[5]   An inhibitor of HIV-1 protease modulates proteasome activity, antigen presentation, and T cell responses [J].
André, P ;
Groettrup, M ;
Klenerman, P ;
de Giuli, R ;
Booth, BL ;
Cerundolo, V ;
Bonneville, M ;
Jotereau, F ;
Zinkernagel, RM ;
Lotteau, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13120-13124
[6]  
Antón LC, 1998, J IMMUNOL, V160, P4859
[7]  
Bai AL, 1997, J IMMUNOL, V159, P2139
[8]   PROTEASOME COMPONENTS WITH RECIPROCAL EXPRESSION TO THAT OF THE MHC-ENCODED LMP PROTEINS [J].
BELICH, MP ;
GLYNNE, RJ ;
SENGER, G ;
SHEER, D ;
TROWSDALE, J .
CURRENT BIOLOGY, 1994, 4 (09) :769-776
[9]   INTERFERON-GAMMA STIMULATION MODULATES THE PROTEOLYTIC ACTIVITY AND CLEAVAGE SITE PREFERENCE OF 20S MOUSE PROTEASOMES [J].
BOES, B ;
HENGEL, H ;
RUPPERT, T ;
MULTHAUP, G ;
KOSZINOWSKI, UH ;
KLOETZEL, PM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (03) :901-909
[10]   Covalent modification of the active site threonine of proteasomal beta subunits and the Escherichia coli homolog HslV by a new class of inhibitors [J].
Bogyo, M ;
McMaster, JS ;
Gaczynska, M ;
Tortorella, D ;
Goldberg, AL ;
Ploegh, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) :6629-6634