Tanaka K, Kasahara M
Tokyo Metropolitan Institute of Medical Science, Bunkyo-ku, Japan.
Immunol Rev. 1998 Jun;163:161-76. doi: 10.1111/j.1600-065x.1998.tb01195.x.
Production of antigenic peptides that serve as MHC class I ligands is essential for initiation of cell-mediated immunity. Accumulating evidence indicates that the proteasome, a large multisubunit protein deg radative machine in eukaryotes, functions as a processing enzyme responsible for the generation of MHC class I ligands. This processing system is elaborately regulated by various immunomodulatory cytokines. In particular, interferon-gamma induces the formation of immunoproteasomes and a recently identified proteasomal regulatory factor. PA28, which in concert contribute to efficient production of MHC class I ligands. Many of the MHC-encoded genes including LMP appear to have emerged by an ancient chromosomal duplication, suggesting that modifications and renewal of pre-existing non-immune genes were instrumental in the emergence of adaptive immunity.
作为MHC I类配体的抗原肽的产生对于细胞介导免疫的启动至关重要。越来越多的证据表明,蛋白酶体是真核生物中一种大型多亚基蛋白质降解机器,作为一种加工酶负责生成MHC I类配体。该加工系统受到各种免疫调节细胞因子的精细调控。特别是,干扰素-γ诱导免疫蛋白酶体和最近鉴定出的蛋白酶体调节因子PA28的形成,它们共同促进MHC I类配体的高效产生。包括LMP在内的许多MHC编码基因似乎是通过古老的染色体复制出现的,这表明对先前存在的非免疫基因的修饰和更新在适应性免疫的出现中发挥了作用。