Nakayama Masafumi
Frontier Research Institute for Interdisciplinary Sciences, Tohoku University , Sendai , Japan.
Front Immunol. 2015 Jan 5;5:672. doi: 10.3389/fimmu.2014.00672. eCollection 2014.
Professional antigen-presenting cells (APCs) such as conventional dendritic cells (DCs) process protein antigens to MHC-bound peptides and then present the peptide-MHC complexes to T cells. In addition to this canonical antigen presentation pathway, recent studies have revealed that DCs and non-APCs can acquire MHC class I (MHCI) and/or MHC class II (MHCII) from neighboring cells through a process of cell-cell contact-dependent membrane transfer called trogocytosis. These MHC-dressed cells subsequently activate or regulate T cells via the preformed antigen peptide-MHC complexes without requiring any further processing. In addition to trogocytosis, intercellular transfer of MHCI and MHCII can be mediated by secretion of membrane vesicles such as exosomes from APCs, generating MHC-dressed cells. This review focuses on the physiological role of antigen presentation by MHCI- or MHCII-dressed cells, and also discusses differences and similarities between trogocytosis and exosome-mediated transfer of MHC.
专业抗原呈递细胞(APC),如传统树突状细胞(DC),将蛋白质抗原加工成与MHC结合的肽,然后将肽-MHC复合物呈递给T细胞。除了这种经典的抗原呈递途径外,最近的研究表明,DC和非APC可以通过一种称为胞啃作用的细胞间接触依赖性膜转移过程,从邻近细胞获取MHC I类(MHCI)和/或MHC II类(MHCII)。这些携带MHC的细胞随后通过预先形成的抗原肽-MHC复合物激活或调节T细胞,而无需任何进一步加工。除了胞啃作用外,MHCI和MHCII的细胞间转移可由APC分泌的膜囊泡(如外泌体)介导,产生携带MHC的细胞。本文综述聚焦于携带MHCI或MHCII的细胞进行抗原呈递的生理作用,并讨论了胞啃作用与外泌体介导的MHC转移之间的异同。