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CD22 regulates thymus-independent responses and the lifespan of B cells.

机译:CD22调节胸腺非依赖性反应和B细胞的寿命。

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摘要

The B-lymphocyte-restricted glycoprotein CD22 is expressed on mature IgM+IgD+ B cells, and is capable of binding to ligands on T and B cells. CD22 can interact with both the B-cell antigen receptor (BCR) complex and signalling molecules, including the protein tyrosine phosphatase SHP1 (PTP1C, SHP), a putative negative regulator of BCR signalling. Thus CD22 may facilitate interactions with lymphocytes and regulate the threshold of BCR signalling. To define the in vivo function of CD22, we generated CD22-deficient mice. Here we show that CD22 is required for normal antibody responses to thymus-independent antigens and regulates the lifespan of mature B cells.
机译:B淋巴细胞限制性糖蛋白CD22在成熟的IgM + IgD + B细胞上表达,并能够与T和B细胞上的配体结合。 CD22可以与B细胞抗原受体(BCR)复合体和信号分子相互作用,包括酪氨酸磷酸酶SHP1蛋白(PTP1C,SHP),一种BCR信号的负调节剂。因此,CD22可促进与淋巴细胞的相互作用并调节BCR信号转导的阈值。为了定义CD22的体内功能,我们产生了CD22缺陷的小鼠。在这里,我们显示CD22是正常的对胸腺非依赖性抗原的抗体应答所必需的,并调节成熟B细胞的寿命。

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