Groothuis T, Neefjes J
Division of Tumor Biology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Curr Top Microbiol Immunol. 2005;300:127-48. doi: 10.1007/3-540-28007-3_6.
MHC class I molecules present small intracellular generated fragments to the outside surveying immune system. This is the result of a series of biochemical processes involving biosynthesis, degradation, translocation, intracellular transport, diffusion, and many more. Critical intermediates and end products of this cascade of events are peptides. The peptides are generated by the proteasome, degraded by peptidases unless transported into the ER where another peptidase and MHC class I molecules are waiting. Unless peptides bind to MHC class I molecules, they are released from the ER and enter the cytoplasm by a system resembling the ERAD pathway in many aspects. The cycle of peptides over the ER membrane with the proteasome at the input site and peptidases or MHC class I molecules on the output site are central in the MHC class I antigen presentation pathway and this review.
MHC I类分子将细胞内产生的小片段呈现给外部的监测免疫系统。这是一系列生化过程的结果,这些过程包括生物合成、降解、转运、细胞内运输、扩散等等。这一系列事件的关键中间体和终产物是肽段。肽段由蛋白酶体产生,除非被转运到内质网(ER),否则会被肽酶降解,而内质网中有另一种肽酶和MHC I类分子在等待。除非肽段与MHC I类分子结合,否则它们会从内质网释放,并通过一个在许多方面类似于内质网相关降解(ERAD)途径的系统进入细胞质。在内质网膜上肽段的循环过程中,蛋白酶体位于输入位点,肽酶或MHC I类分子位于输出位点,这在MHC I类抗原呈递途径以及本综述中处于核心地位。