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内吞作用机制与抗原呈递的细胞生物学

Endocytosis mechanisms and the cell biology of antigen presentation.

作者信息

Burgdorf Sven, Kurts Christian

机构信息

Institute of Molecular Medicine and Experimental Immunology (IMMEI), Friedrich-Wilhelms-Universität, Bonn, Germany.

出版信息

Curr Opin Immunol. 2008 Feb;20(1):89-95. doi: 10.1016/j.coi.2007.12.002. Epub 2008 Jan 30.

Abstract

Recent evidence revealed that presentation of soluble antigens is governed by the endocytosis mechanisms that determine the intracellular routing of the endocytosed antigens. Soluble antigens intended for classical exogenous MHC-II-restricted presentation are internalized into lysosomes. Soluble antigens destined for crosspresentation are taken up by distinct endocytosis mechanisms and are conveyed into stable early endosomes. Particulate antigens enter phagosomes, in which both MHC-I-restricted and MHC-II-restricted presentation is initiated. In this review, we discuss the mechanistical differences in presentation of soluble and particulate antigen, the correlation of various endocytic receptors with antigen routing and presentation, the differential expression of these receptors in antigen-presenting cell subsets with respect to their ability to crosspresent, and implications on the molecular mechanisms controlling cross-presentation.

摘要

最近的证据表明,可溶性抗原的呈递受内吞作用机制的调控,这些机制决定了内吞抗原在细胞内的转运途径。用于经典外源性MHC-II限制性呈递的可溶性抗原被内化到溶酶体中。用于交叉呈递的可溶性抗原通过不同的内吞作用机制被摄取,并被转运到稳定的早期内体中。颗粒性抗原进入吞噬体,在其中启动MHC-I限制性和MHC-II限制性呈递。在本综述中,我们讨论了可溶性和颗粒性抗原呈递的机制差异、各种内吞受体与抗原转运和呈递的相关性、这些受体在抗原呈递细胞亚群中关于其交叉呈递能力的差异表达,以及对控制交叉呈递的分子机制的影响。

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