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MHC class II antigen presentation

Reactome ID: R-HSA-2132295

中文名称

MHC II 类抗原呈递

通路描述

抗原呈递细胞(如 B 细胞、树突状细胞和单核/巨噬细胞)在其表面表达主要组织相容性复合体 II 类分子(MHC II),并将外源性抗原肽呈递给 CD4+ T 辅助细胞。CD4+ T 细胞在免疫保护中起核心作用。在激活后,它们刺激 B 细胞分化为产生抗体的 B 细胞前体,并启动适应性免疫反应。MHC II 类分子是跨膜糖蛋白异二聚体,由α和β亚基组成。新合成的 MHC II 类分子在内质网中呈递时,与一种称为不变链(Ii)的伴侣蛋白结合。Ii 的结合防止新生 MHC 分子在 ER 中过早结合自抗原,并引导 MHC 分子进入吞噬细胞器。在内质网酸性环境中,Ii 以步骤方式降解,最终释放 MHC II 类肽结合槽,以便装载抗原肽。外源性抗原通过受体介导的内吞作用、吞噬作用或胞饮作用被 APC 摄入 MHC II 类阳性细胞的吞噬细胞器,在这些酸性环境中由多种酸性蛋白酶降解,生成 MHC II 类表位。抗原肽随后装载到 MHC II 类配体结合槽中。形成的 MHC II 类肽复合物随后移动到细胞表面,CD4+ T 细胞对其进行扫描以进行特异性识别(Berger & Roche 2009, Zhou & Blum 2004, Watts 2004, Landsverk et al. 2009)。
英文描述
MHC class II antigen presentation Antigen presenting cells (APCs) such as B cells, dendritic cells (DCs) and monocytes/macrophages express major histocompatibility complex class II molecules (MHC II) at their surface and present exogenous antigenic peptides to CD4+ T helper cells. CD4+ T cells play a central role in immune protection. On their activation they stimulate differentiation of B cells into antibody-producing B-cell blasts and initiate adaptive immune responses. MHC class II molecules are transmembrane glycoprotein heterodimers of alpha and beta subunits. Newly synthesized MHC II molecules present in the endoplasmic reticulum bind to a chaperone protein called invariant (Ii) chain. The binding of Ii prevents the premature binding of self antigens to the nascent MHC molecules in the ER and also guides MHC molecules to endocytic compartments. In the acidic endosomal environment, Ii is degraded in a stepwise manner, ultimately to free the class II peptide-binding groove for loading of antigenic peptides. Exogenous antigens are internalized by the APC by receptor mediated endocytosis, phagocytosis or pinocytosis into endocytic compartments of MHC class II positive cells, where engulfed antigens are degraded in a low pH environment by multiple acidic proteases, generating MHC class II epitopes. Antigenic peptides are then loaded into the class II ligand-binding groove. The resulting class II peptide complexes then move to the cell surface, where they are scanned by CD4+ T cells for specific recognition (Berger & Roche 2009, Zhou & Blum 2004, Watts 2004, Landsverk et al. 2009).

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