Mukherjee Rinee, Chaturvedi Pratibha, Lee-Chan Edwin, Singh Bhagirath
Department of Microbiology and Immunology and Robarts Research Institute, University of Western Ontario, London, Ontario, Canada N6A 5C1.
Mol Immunol. 2008 Apr;45(8):2166-76. doi: 10.1016/j.molimm.2007.12.016. Epub 2008 Feb 15.
We have previously shown that exogenous CLIP (class II associated invariant chain peptide) downregulated MHC class II expression on antigen presenting cells (APC) and modulated T cell mediated immune responses. The present study was undertaken to investigate the mechanism of uptake of exogenously added CLIP peptide by APC. We found that exogenous CLIP is rapidly internalized by APC and it co-localize with MHC class II in intracellular compartments including early-, late-endosomes and lysosomes. We suggest that exogenous CLIP acts as an in vivo regulator of immune response by internalization and passage through the intracellular compartments where it interferes in peptide loading and recycling of MHC class II molecules to the APC surface. Therefore, exogenous CLIP regulates immune responses by modulation of antigen presentation by the APC.
我们之前已经表明,外源性CLIP(II类相关恒定链肽)下调抗原呈递细胞(APC)上的MHC II类表达,并调节T细胞介导的免疫反应。本研究旨在探讨APC对外源性添加的CLIP肽的摄取机制。我们发现外源性CLIP被APC迅速内化,并与MHC II类在包括早期、晚期内体和溶酶体在内的细胞内区室中共定位。我们认为外源性CLIP通过内化并穿过细胞内区室来充当免疫反应的体内调节剂,在这些区室中它干扰MHC II类分子的肽装载和循环至APC表面。因此,外源性CLIP通过调节APC的抗原呈递来调节免疫反应。