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早期人类T细胞激活事件与表面II类主要组织相容性复合体的结合。

Early human T cell activation events with engagement of surface MHC class II.

作者信息

King R L, Nguyen Q V

机构信息

Department of Pediatrics, State University of New York Health Science Center, Syracuse 13210, USA.

出版信息

J Cell Biochem. 1998 Sep 1;70(3):346-53.

PMID:9706872
Abstract

Major histocompatibility complex (MHC) class II are expressed on most activated human lymphocytes. They direct antigen presentation events in dendritic cells and B cells (collectively called antigen presenting cells), but the role for MHC class II in human T cells is not well understood. To understand the role of surface MHC class II and to identify the molecules involved in signaling, we have defined the early activation sequence in T cells when MHC class II are engaged by a specific antibody. Specifically, we have characterized the involvement of phosphotyrosine kinases, phospholipase C (PLC), and Ca2+ mobilization. With the engagement by either whole anti-class II antibody or its Fab fragments, the enzymatic activity of p56lck and ZAP-70 increased, but there was no increase in p59fyn activity. In addition, the intracellular free Ca2+ increased, which was due to enhanced influx and not to the mobilization of intracytoplasmic Ca2+. These events did not require cross-linking because they were not significantly augmented by the addition of antispecies antibody. The coimmunoprecipitation of tyrosine phosphorylated PLC-gamma1 with surface MHC class II suggested that PLC-gamma1 could be recruited to MHC class II after engagement. These results show the complexities of the early signals transduced by the engagement of surface MHC class II on T cells.

摘要

主要组织相容性复合体(MHC)II类分子在大多数活化的人淋巴细胞上表达。它们指导树突状细胞和B细胞(统称为抗原呈递细胞)中的抗原呈递过程,但MHC II类分子在人T细胞中的作用尚未完全了解。为了了解表面MHC II类分子的作用并确定参与信号传导的分子,我们定义了T细胞中MHC II类分子与特异性抗体结合时的早期激活序列。具体而言,我们已经表征了磷酸酪氨酸激酶、磷脂酶C(PLC)和Ca2+动员的参与情况。当与完整的抗II类抗体或其Fab片段结合时,p56lck和ZAP-70的酶活性增加,但p59fyn活性没有增加。此外,细胞内游离Ca2+增加,这是由于流入增强而非细胞质内Ca2+的动员所致。这些事件不需要交联,因为添加抗种属抗体并没有显著增强它们。酪氨酸磷酸化的PLC-γ1与表面MHC II类分子的共免疫沉淀表明,PLC-γ1在结合后可以被招募到MHC II类分子上。这些结果显示了表面MHC II类分子与T细胞结合所转导的早期信号的复杂性。

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