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鼠巨细胞病毒糖蛋白gp40的腔内部位催化MHC I类分子的滞留。

The luminal part of the murine cytomegalovirus glycoprotein gp40 catalyzes the retention of MHC class I molecules.

作者信息

Ziegler H, Muranyi W, Burgert H G, Kremmer E, Koszinowski U H

机构信息

Max-von-Pettenkofer Institut, Genzentrum, Ludwig-Maximilians-Universität München, Germany.

出版信息

EMBO J. 2000 Mar 1;19(5):870-81. doi: 10.1093/emboj/19.5.870.

DOI:10.1093/emboj/19.5.870
PMID:10698929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC305627/
Abstract

Murine cytomegalovirus (MCMV) interferes with the MHC class I pathway of antigen presentation. The type I transmembrane glycoprotein gp40, encoded by the gene m152, retains major histocompatibility complex (MHC) class I complexes in the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC)/cis-Golgi. These MHC class I complexes are stable, show an extended half-life and do not exchange beta(2)-microglobulin, whereas gp40 reaches an endosomal/lysosomal compartment where it subsequently is degraded. The analysis of regions within the viral protein that are essential for MHC class I retention revealed that a secreted form of gp40, lacking the cytoplasmic tail and the transmembrane region, still has the capacity to retain MHC class I complexes. Continuous expression of gp40 is not required for MHC class I retention. Our data indicate that the retention of MHC class I complexes in the ERGIC/cis-Golgi is triggered by gp40 and does not require the further presence of the viral protein.

摘要

小鼠巨细胞病毒(MCMV)干扰抗原呈递的MHC I类途径。由基因m152编码的I型跨膜糖蛋白gp40将主要组织相容性复合体(MHC)I类复合体保留在内质网(ER)-高尔基体中间区室(ERGIC)/顺式高尔基体中。这些MHC I类复合体是稳定的,具有延长的半衰期,并且不交换β2-微球蛋白,而gp40到达内体/溶酶体区室,随后在那里被降解。对病毒蛋白中对于MHC I类保留至关重要的区域的分析表明,缺乏细胞质尾巴和跨膜区域的分泌形式的gp40仍然具有保留MHC I类复合体的能力。MHC I类保留不需要gp40的持续表达。我们的数据表明,gp40触发了MHC I类复合体在ERGIC/顺式高尔基体中的保留,并且不需要病毒蛋白的进一步存在。

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本文引用的文献

1
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EMBO J. 1999 Feb 15;18(4):1081-91. doi: 10.1093/emboj/18.4.1081.
2
Immune evasion by cytomegalovirus--survival strategies of a highly adapted opportunist.巨细胞病毒的免疫逃逸——一种高度适应性机会病原体的生存策略
Trends Microbiol. 1998 May;6(5):190-7. doi: 10.1016/s0966-842x(98)01255-4.
3
Mechanisms of MHC class I--restricted antigen processing.MHC I类分子限制性抗原加工机制
Annu Rev Immunol. 1998;16:323-58. doi: 10.1146/annurev.immunol.16.1.323.
4
Herpesvirus evasion of the immune system.疱疹病毒对免疫系统的逃避
Curr Top Microbiol Immunol. 1998;232:149-77. doi: 10.1007/978-3-642-72045-1_8.
5
Interference with antigen processing by viruses.病毒对抗原加工的干扰。
Curr Opin Immunol. 1997 Aug;9(4):470-6. doi: 10.1016/s0952-7915(97)80097-0.
6
The human cytomegalovirus US6 glycoprotein inhibits transporter associated with antigen processing-dependent peptide translocation.人类巨细胞病毒US6糖蛋白抑制与抗原加工相关的转运体依赖性肽易位。
Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):6904-9. doi: 10.1073/pnas.94.13.6904.
7
A viral ER-resident glycoprotein inactivates the MHC-encoded peptide transporter.一种病毒内质网驻留糖蛋白可使主要组织相容性复合体(MHC)编码的肽转运体失活。
Immunity. 1997 May;6(5):623-32. doi: 10.1016/s1074-7613(00)80350-7.
8
The ER-luminal domain of the HCMV glycoprotein US6 inhibits peptide translocation by TAP.人巨细胞病毒糖蛋白US6的内质网腔结构域可抑制抗原加工相关转运体(TAP)介导的肽转运。
Immunity. 1997 May;6(5):613-21. doi: 10.1016/s1074-7613(00)80349-0.
9
Transmembrane domain-dependent sorting of proteins to the ER and plasma membrane in yeast.酵母中蛋白质通过跨膜结构域依赖性分选至内质网和质膜
EMBO J. 1997 Apr 15;16(8):1832-41. doi: 10.1093/emboj/16.8.1832.
10
Dissociation of coatomer from membranes is required for brefeldin A-induced transfer of Golgi enzymes to the endoplasmic reticulum.衣被蛋白从膜上解离是布雷菲德菌素A诱导高尔基体酶向内质网转移所必需的。
J Cell Biol. 1997 Apr 21;137(2):319-33. doi: 10.1083/jcb.137.2.319.