SELECTIVE DEVELOPMENT OF CD4+ T-CELLS IN TRANSGENIC MICE EXPRESSING A CLASS-II MHC-RESTRICTED ANTIGEN RECEPTOR
SELECTIVE DEVELOPMENT OF CD4+ T-CELLS IN TRANSGENIC MICE EXPRESSING A CLASS-II MHC-RESTRICTED ANTIGEN RECEPTOR
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DOI:
10.1038/341746a0
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发表时间:
1989-10-26
期刊:
影响因子:
64.8
通讯作者:
HEDRICK, SM
中科院分区:
文献类型:
--
作者:
KAYE, J;HSU, ML;HEDRICK, SM
T LYMPHOCYTES are predisposed to recognition of foreign protein fragments bound to cell-surface molecules encoded by the major histocompatibility complex (MHC)1, 2. There is now compelling evidence that this specificity is a consequence of a selection process operating on developing T lymphocytes in the thymus3–6. As a result of this positive selection, thymocytes that express antigen receptors with a threshold affinity for self MHC-encoded glycoproteins preferentially emigrate from the thymus and seed peripheral lymphoid organs. The specificity for both foreign antigen and MHC molecules is imparted by theαandβchains of the T-cell antigen receptor (TCR)7, 8. Two other T-cell surface proteins, CD4 and CD8, which bind non-polymorphic regions of class II and class I MHC molecules respectively9, 10, are also involved in these recognition events and play an integral role in thymic selection. In order to elucidate the developmental pathways of class II MHC-rest rioted T cells in relation to these essential accessory molecules, we have produced TCR-transgenic mice expressing a receptor specific for a fragment of pigeon cytochrome c and the Ek(class II MHC) molecule. The transgenic TCR is expressed on virtually all T cells in mice expressingk. The thymuses of these mice contain an abnormally high percentage of mature CD4+CD8−cells. In addition, the peripheral T-cell population is almost exclusively CD4+, demonstrating that the MHC specificity of the TCR determines the phenotype of T cells during selection in the thymus.