首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Requirement of SH2-containing Protein Tyrosine Phosphatases SHP-1 and SHP-2 for Paired Immunoglobulin-like Receptor B (PIR-B)–mediated Inhibitory Signal
【2h】

Requirement of SH2-containing Protein Tyrosine Phosphatases SHP-1 and SHP-2 for Paired Immunoglobulin-like Receptor B (PIR-B)–mediated Inhibitory Signal

机译:含SH2的蛋白酪氨酸磷酸酶SHP-1和SHP-2对成对的免疫球蛋白样受体B(PIR-B)介导的抑制信号的要求

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Paired immunoglobulin-like receptor B (PIR-B) (p91) molecule has been proposed to function as an inhibitory receptor in B cells and myeloid lineage cells. We demonstrate here that the cytoplasmic region of PIR-B is capable of inhibiting B cell activation. Mutational analysis of five cytoplasmic tyrosines indicate that tyrosine 771 in the motif VxYxxL plays the most crucial role in mediating the inhibitory signal. PIR-B–mediated inhibition was markedly reduced in the SH2-containing protein tyrosine phosphatases SHP-1 and SHP-2 double-deficient DT40 B cells, whereas this inhibition was unaffected in the inositol polyphosphate 5′-phosphatase SHIP-deficient cells. These data demonstrate that PIR-B can negatively regulate B cell receptor activation and that this PIR-B–mediated inhibition requires redundant functions of SHP-1 and SHP-2.
机译:已提出成对的免疫球蛋白样受体B(PIR-B)(p91)分子在B细胞和髓系细胞中起抑制性受体的作用。我们在这里证明,PIR-B的胞质区域能够抑制B细胞活化。对五个胞质酪氨酸的突变分析表明,基序VxYxxL中的酪氨酸771在介导抑制信号中起着至关重要的作用。在含有SH2的蛋白酪氨酸磷酸酶SHP-1和SHP-2双缺陷DT40 B细胞中,PIR-B介导的抑制作用显着降低,而在肌醇多磷酸5'-磷酸酶SHIP缺陷细胞中,这种抑制作用不受影响。这些数据表明,PIR-B可以负调控B细胞受体的活化,并且这种PIR-B介导的抑制作用需要SHP-1和SHP-2的冗余功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号