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CD1d 呈递溶血磷脂并被人类自然杀伤 T 细胞受体识别。

Lysophospholipid presentation by CD1d and recognition by a human Natural Killer T-cell receptor.

机构信息

Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.

出版信息

EMBO J. 2012 Apr 18;31(8):2047-59. doi: 10.1038/emboj.2012.54. Epub 2012 Mar 6.

Abstract

Invariant Natural Killer T (iNKT) cells use highly restricted αβ T cell receptors (TCRs) to probe the repertoire of lipids presented by CD1d molecules. Here, we describe our studies of lysophosphatidylcholine (LPC) presentation by human CD1d and its recognition by a native, LPC-specific iNKT TCR. Human CD1d presenting LPC adopts an altered conformation from that of CD1d presenting glycolipid antigens, with a shifted α1 helix resulting in an open A' pocket. Binding of the iNKT TCR requires a 7-Å displacement of the LPC headgroup but stabilizes the CD1d-LPC complex in a closed conformation. The iNKT TCR CDR loop footprint on CD1d-LPC is anchored by the conserved positioning of the CDR3α loop, whereas the remaining CDR loops are shifted, due in part to amino-acid differences in the CDR3β and Jβ segment used by this iNKT TCR. These findings provide insight into how lysophospholipids are presented by human CD1d molecules and how this complex is recognized by some, but not all, human iNKT cells.

摘要

天然不变自然杀伤 T(iNKT)细胞使用高度受限的αβ T 细胞受体(TCR)来探测 CD1d 分子呈递的脂质谱。在这里,我们描述了我们对人 CD1d 呈递溶血磷脂酰胆碱(LPC)及其与天然、LPC 特异性 iNKT TCR 识别的研究。人 CD1d 呈递 LPC 采用与呈递糖脂抗原不同的构象,α1 螺旋移位导致开放的 A'口袋。iNKT TCR 的结合需要 LPC 头部基团 7Å 的位移,但稳定了封闭构象的 CD1d-LPC 复合物。iNKT TCR CDR 环在 CD1d-LPC 上的足迹由 CDR3α 环的保守定位锚定,而其余 CDR 环发生位移,部分原因是该 iNKT TCR 使用的 CDR3β 和 Jβ 片段的氨基酸差异。这些发现提供了关于人 CD1d 分子如何呈递溶血磷脂以及该复合物如何被一些(但不是全部)人 iNKT 细胞识别的见解。

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