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鼠巨细胞病毒编码的I类主要组织相容性复合体同源物m144对自然杀伤细胞的抑制作用。

Inhibition of NK cells by murine CMV-encoded class I MHC homologue m144.

作者信息

Kubota A, Kubota S, Farrell H E, Davis-Poynter N, Takei F

机构信息

Terry Fox Laboratory, British Columbia Cancer Agency, British Columbia, Canada.

出版信息

Cell Immunol. 1999 Feb 1;191(2):145-51. doi: 10.1006/cimm.1998.1424.

Abstract

Murine cytomegalovirus (CMV)-encoded protein m144 is homologous to class I MHC heavy-chain and is thought to regulate NK-cell-mediated immune responses in vivo. To examine the effects of m144 on NK cytotoxicity in vitro, various cell lines were transfected with wild-type m144 or a chimeric construct in which the cytoplasmic domain of m144 was replaced with green fluorescence protein. Burkitt lymphoma line Raji expressed a significant level of m144 as determined by anti-m144 mAb binding or the green fluorescence of the fusion protein. The level of m144 expression was relatively low compared with that of transfected murine class I MHC Dd. However, m144 on Raji cells partially inhibited antibody-dependent cell-mediated cytotoxicity of IL-2-activated NK cells. NK cells from the CMV-susceptible BALB/c as well as those from the resistant C57BL/6 mice were inhibited by m144. Antibodies against the known murine NK inhibitory receptors Ly-49A, C, G, and I did not affect the inhibitory effect of m144. These results suggest that the murine CMV class I MHC homologue m144 partially inhibits NK cells by interacting with a novel inhibitory receptor.

摘要

小鼠巨细胞病毒(CMV)编码的蛋白m144与I类主要组织相容性复合体(MHC)重链同源,被认为在体内调节自然杀伤细胞(NK细胞)介导的免疫反应。为了在体外检测m144对NK细胞毒性的影响,用野生型m144或一种嵌合构建体转染各种细胞系,该嵌合构建体中m144的胞质结构域被绿色荧光蛋白取代。通过抗m144单克隆抗体结合或融合蛋白的绿色荧光测定,伯基特淋巴瘤细胞系Raji表达显著水平的m144。与转染的小鼠I类MHC Dd相比,m144的表达水平相对较低。然而,Raji细胞上的m144部分抑制了IL-2激活的NK细胞的抗体依赖性细胞介导的细胞毒性。来自CMV易感的BALB/c小鼠以及抗性的C57BL/6小鼠的NK细胞均被m144抑制。针对已知的小鼠NK抑制性受体Ly-49A、C、G和I的抗体不影响m144的抑制作用。这些结果表明,小鼠CMV的I类MHC同源物m144通过与一种新型抑制性受体相互作用来部分抑制NK细胞。

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