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受体介导的 T 细胞对抗原提呈细胞来源分子的摄取。

Receptor-mediated T cell absorption of antigen presenting cell-derived molecules.

机构信息

Department of Chemistry and Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.

出版信息

Front Biosci (Landmark Ed). 2011 Jan 1;16(2):411-21. doi: 10.2741/3695.

Abstract

T cells tend to acquire a variety of cell surface molecules derived from antigen presenting cells (APCs). The molecule uptake occurs mainly during direct T/APC contact and is instigated by specific receptor/ligand interactions, such as T cell receptor (TCR) with a cognate peptide/MHC complex (pMHC) or CD28 with B7. The acquired molecules are targeted for internalization and degradation in the lysosome. Nevertheless, those molecules are expressed on the surface of T cells for a period of time. The presentation of APC-derived ligands by T cells exhibited a multitude of immunological effects via antigen-specific T/T interaction upon recognition of the absorbed antigens by contact with other T cells. Ligand uptake also occurs via absorption of membrane vesicles shed from APCs prior to contact (e.g., exosomes and plasma membrane-derived vesicles). As in ligand absorption via direct T/APC interaction, the absorption of pre-formed membrane vesicles is also dependent on specific receptor/ligand interactions. In this review, biological mechanisms underlying the ligand absorption process as well as the biological significance and application of the event will be discussed.

摘要

T 细胞倾向于获取源自抗原呈递细胞 (APC) 的多种细胞表面分子。分子摄取主要发生在直接的 T/APC 接触期间,并由特定的受体/配体相互作用引发,例如 T 细胞受体 (TCR) 与同源肽/MHC 复合物 (pMHC) 或 CD28 与 B7 的相互作用。所获取的分子被靶向用于内吞和溶酶体降解。然而,这些分子在 T 细胞表面表达一段时间。T 细胞呈现 APC 衍生的配体,通过与其他 T 细胞接触识别吸收的抗原,通过抗原特异性 T/T 相互作用表现出多种免疫效应。配体摄取也通过吸收 APC 接触前脱落的膜囊泡(例如外泌体和质膜衍生的囊泡)来发生。与直接的 T/APC 相互作用中的配体吸收一样,预先形成的膜囊泡的吸收也依赖于特定的受体/配体相互作用。在这篇综述中,将讨论配体吸收过程的生物学机制以及该事件的生物学意义和应用。

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