Structural compartmentalization of MHC class II signaling function.
Structural compartmentalization of MHC class II signaling function.
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MHC II 类信号传导功能的结构划分。
DOI:
10.1016/0167-5699(93)90184-m
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发表时间:
1993
期刊:
影响因子:
--
通讯作者:
Cambier,JC
中科院分区:
文献类型:
--
作者:
Wade,WF;Davoust,J;Salamero,J;Andre,P;Watts,TH;Cambier,JC
Major histocompatibility complex (MHC) class II molecules are critical restricting elements in the generation of thymus-dependent immune responses. Recent studies indicate that in addition to providing a composite epitope for recognition by T-ceU antigen receptors, MHC class II molecules function in signal transduction through interaction with other celhdar proteins. Mutational analyses indicate that structural information necessary for these functions is compartmentalized in different aspects of the molecular complex. Here, William Wade and colleagues review the structual basis of this MHC class II function as defined in the I-Act and-[3 chains.Generation of antibody (Ab) responses to protein antigens (Ag) requires the physical interaction of Ag presenting cells (APC) and T cells. The B cell is an efficient APC because of its ability to concentrate Ag via its Ag-specific receptors and its expression of various accessory ligands which stimulate T cells. The specificity of the interaction between T and B lymphocytes is determined by peptide fragments of Ag bound to B-cell major histocompatibility complex (MHC) class II molecules and the T-cell Ag-specific receptor (TCR). Agspecific interaction mediated by MHC class II and TCR can lead to the activation and proliferation of