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The comings and goings of MHC class I molecules herald a new dawn in cross-presentation

机译:MHC I类分子的来往预示着交叉展示的新曙光

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MHC class I (MHC-I) molecules are the centerpieces of cross-presentation. They are loaded with peptides derived from exogenous sources and displayed on the plasma membrane to communicate with CD8 T cells, relaying a message of tolerance or attack. The study of cross-presentation has been focused on the relative contributions of the vacuolar versus cytosolic pathways of antigen processing and the location where MHC-I molecules are loaded. While vacuolar processing generates peptides loaded onto vacuolar MHC-I molecules, how and where exogenous peptides generated by the proteasome and transported by TAP meet MHC-I molecules for loading has been a matter of debate. The source and trafficking of MHC-I molecules in dendritic cells have largely been ignored under the expectation that these molecules came from the Endoplasmic reticulum (ER) or the plasma membrane. New studies reveal a concentrated pool of MHC-I molecules in the endocytic recycling compartment (ERC). These pools are rapidly mobilized to phagosomes carrying microbial antigens, and in a signaldependent manner under the control of Toll-like receptors. The phagosome becomes a dynamic hub receiving traffic from multiple sources, the ER-Golgi intermediate compartment for delivering the peptideloading machinery and the ERC for deploying MHC-I molecules that alert CD8 T cells of infection.
机译:MHC I类(MHC-1)分子是交叉展示的核心。它们装载有来自外源性来源的肽,并显示在质膜上,可与CD8 T细胞进行通讯,传达耐受性或攻击性信息。交叉呈递的研究集中于液泡相对于抗原加工的胞质途径的相对贡献以及装载MHC-1分子的位置。虽然液泡加工产生了加载到液泡MHC-1分子上的肽,但是由蛋白酶体产生并由TAP转运的外源肽如何以及在何处与MHC-1分子结合以进行加载一直是一个争论的问题。在预期这些分子来自内质网(ER)或质膜的情况下,树突状细胞中MHC-1分子的来源和运输已被大大忽略。新的研究表明,内吞循环室(ERC)中有MHC-1分子的浓缩池。这些库在Toll样受体的控制下以信号依赖的方式迅速动员到携带微生物抗原的吞噬体。吞噬体成为一个动态枢纽,从多个来源接收流量,其中ER-Golgi中间隔室用于输送多肽加载机器,而ERC则用于部署MHC-1分子以警告CD8 T细胞感染。

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