Peterson M, Miller J
Department of Molecular Genetics and Cell Biology, University of Chicago, Illinois 60637.
Nature. 1992 Jun 18;357(6379):596-8. doi: 10.1038/357596a0.
During biosynthesis, class II molecules of the major histocompatibility complex are associated with a nonpolymorphic protein called invariant chain, Ii, which facilitates folding of class II molecules and their exit from the endoplasmic reticulum, interferes with their association with peptide and directs their post-Golgi transport (refs 7-9). If Ii blocks class II loading with endogenous antigens in the endoplasmic reticulum and/or directs class II molecules to the exogenous antigen-loading compartment, then the co-expression of Ii should enhance the ability of class II molecules to present exogenous antigens to T cells. But data supporting a role for Ii in class II-restricted antigen presentation are controversial. Here we show that Ii can facilitate exogenous antigen presentation for a subset of antigens. Although all known functions of Ii have been ascribed to the principal form of Ii, p31, we find that in most cases antigen presentation is facilitated only by the alternatively spliced, minor form of Ii, p41.
在生物合成过程中,主要组织相容性复合体的II类分子与一种名为恒定链(Ii)的非多态性蛋白质相关联,该蛋白质促进II类分子的折叠及其从内质网的输出,干扰它们与肽的结合,并指导它们在高尔基体后的运输(参考文献7 - 9)。如果Ii在内质网中阻止II类分子加载内源性抗原和/或指导II类分子进入外源性抗原加载区室,那么Ii的共表达应该增强II类分子向外周血T细胞呈递外源性抗原的能力。但是支持Ii在II类限制性抗原呈递中起作用的数据存在争议。在这里,我们表明Ii可以促进一部分抗原的外源性抗原呈递。尽管Ii的所有已知功能都归因于Ii的主要形式p31,但我们发现,在大多数情况下,抗原呈递仅由Ii的可变剪接的次要形式p41促进。