Natarajan K, Li H, Mariuzza R A, Margulies D H
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-1892, USA.
Rev Immunogenet. 1999;1(1):32-46.
MHC class I molecules (MHC-I) are cell surface recognition elements expressed on virtually all somatic cells. These molecules sample peptides generated within the cell and signal the cell's physiological state to effector cells of the immune system, both T lymphocytes and natural killer (NK) cells. In addition, molecules structurally related to MHC-I, collectively known as MHC-Ib, are more specialized and, in some cases, interact with more limited subsets of lymphoid cells. Using the recently determined structure of the classical MHC-I molecule, H-2Dd, as a paradigm for structure and function, we review other MHC-I and MHC-Ib molecules, with an emphasis on how the same basic structural fold is employed by classical MHC-I molecules to bind specific peptides and T cell receptors, and is exploited by the MHC-Ib molecules in more stringent molecular interactions. It is instructive that structurally related molecules have evolved to perform a number of unique and distinct functions in immune and non-immune recognition.
MHC I类分子(MHC-I)是几乎在所有体细胞上表达的细胞表面识别元件。这些分子对细胞内产生的肽进行取样,并将细胞的生理状态信号传递给免疫系统的效应细胞,即T淋巴细胞和自然杀伤(NK)细胞。此外,与MHC-I结构相关的分子,统称为MHC-Ib,更为特殊,在某些情况下,与更有限的淋巴细胞亚群相互作用。以最近确定的经典MHC-I分子H-2Dd的结构作为结构和功能的范例,我们综述了其他MHC-I和MHC-Ib分子,重点关注经典MHC-I分子如何利用相同的基本结构折叠来结合特定的肽和T细胞受体,以及MHC-Ib分子如何在更严格的分子相互作用中加以利用。具有指导意义的是,结构相关的分子已经进化到在免疫和非免疫识别中执行许多独特和不同的功能。