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MHC I 相关自身肽的起源和可塑性。

Origin and plasticity of MHC I-associated self peptides.

机构信息

Institute for Research in Immunology and Cancer (IRIC), Université de Montréal, Montreal, Canada.

出版信息

Autoimmun Rev. 2012 Jul;11(9):627-35. doi: 10.1016/j.autrev.2011.11.003. Epub 2011 Nov 12.

Abstract

Endogenous peptides presented by MHC I molecules represent the essence of self for CD8 T lymphocytes. These MHC I peptides (MIPs) regulate all key events that occur during the lifetime of CD8 T cells. CD8 T cells are selected on self-MIPs, sustained by self-MIPs, and activated in the presence of self-MIPs. Recently, large-scale mass spectrometry studies have revealed that the self-MIP repertoire is more complex and plastic than previously anticipated. The composition of the self-MIP repertoire varies from one cell type to another and can be perturbed by cell-intrinsic and -extrinsic factors including dysregulation of cellular metabolism and infection. The complexity and plasticity of the self-MIP repertoire represent a major challenge for the maintenance of self tolerance and can have pervasive effects on the global functioning of the immune system.

摘要

内源性肽由 MHC I 分子呈递,代表了 CD8 T 淋巴细胞的自身本质。这些 MHC I 肽(MIP)调节 CD8 T 细胞一生中发生的所有关键事件。CD8 T 细胞在自身 MIP 上被选择,由自身 MIP 维持,并在自身 MIP 存在的情况下被激活。最近,大规模质谱研究表明,自身 MIP 库比以前预期的更复杂和有弹性。自身 MIP 库的组成因细胞类型而异,并且可以受到细胞内在和外在因素的干扰,包括细胞代谢失调和感染。自身 MIP 库的复杂性和弹性是维持自身耐受的主要挑战,并且会对免疫系统的整体功能产生广泛影响。

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