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自然杀伤细胞克隆识别MHC I类分子时的肽特异性

Peptide specificity in the recognition of MHC class I by natural killer cell clones.

作者信息

Malnati M S, Peruzzi M, Parker K C, Biddison W E, Ciccone E, Moretta A, Long E O

机构信息

Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Rockville, MD 20852.

出版信息

Science. 1995 Feb 17;267(5200):1016-8. doi: 10.1126/science.7863326.

Abstract

Recognition by natural killer (NK) cells of major histocompatibility complex (MHC) class I molecules on target cells inhibits NK-mediated lysis. Here, inhibition of NK clones by HLA-B2705 molecules mutated at single amino acids in the peptide binding site varied among HLA-B2705-specific NK clones. In addition, a subset of such NK clones was inhibited by only one of several self peptides loaded onto HLA-B*2705 molecules expressed in peptide transporter-deficient cells, showing that recognition was peptide-specific. These data demonstrate that specific self peptides, complexed with MHC class I, provide protection from NK-mediated lysis.

摘要

自然杀伤(NK)细胞对靶细胞上主要组织相容性复合体(MHC)I类分子的识别会抑制NK介导的细胞裂解。在此,肽结合位点单个氨基酸发生突变的HLA - B2705分子对NK克隆的抑制作用在HLA - B2705特异性NK克隆中存在差异。此外,此类NK克隆的一个亚群仅被加载到肽转运缺陷细胞中表达的HLA - B*2705分子上的几种自身肽中的一种所抑制,这表明识别具有肽特异性。这些数据证明,与MHC I类分子复合的特定自身肽可提供免受NK介导细胞裂解的保护。

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