...
首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Species restriction of Herpesvirus saimiri and Herpesvirus ateles: Human lymphocyte transformation correlates with distinct signaling properties of viral oncoproteins
【24h】

Species restriction of Herpesvirus saimiri and Herpesvirus ateles: Human lymphocyte transformation correlates with distinct signaling properties of viral oncoproteins

机译:疱疹病毒saimiri和疱疹病毒属的物种限制:人类淋巴细胞转化与病毒癌蛋白独特的信号传导特性相关

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The potential of Herpesvirus saimiri (HVS) subgroups A, B and C and Herpesvirus ateles (HVA) to transform primary T cells to permanent growth in vitro is restricted by the primate host species and by viral variability represented by distinct viral oncoproteins. We now addressed the relation between the transforming potential of the different viruses and the signaling pathways activated by transiently expressed oncoproteins. Marmoset lymphocytes were transformed by all HVS subgroups as well as HVA, while transformation of human cells was restricted to HVS-C and, unexpectedly, HVA. NF-κB and Src-family kinase (SFK) activity was required for survival of all transformed lymphocytes. Accordingly, NF-κB was induced by oncoproteins of all viruses. In contrast, SFK-related signaling was detectable only for oncoproteins of HVS-C and HVA. Thus, the restricted transformation of human lymphocytes likely correlates with the specific SFK targeting by these oncoproteins. These results will enable further studies into novel SFK effector mechanisms relevant for T-cell proliferation.
机译:灵长类动物宿主物种和以独特的病毒癌蛋白代表的病毒变异性限制了疱疹病毒saimiri(HVS)亚组,B和C亚群和疱疹病毒亚纲(HVA)在体外将原代T细胞转化为永久性生长的潜力。现在,我们解决了不同病毒的转化潜能与瞬时表达的癌蛋白激活的信号通路之间的关系。 H猴淋巴细胞被所有HVS亚组和HVA转化,而人类细胞的转化仅限于HVS-C和意想不到的HVA。所有转化淋巴细胞的存活都需要NF-κB和Src家族激酶(SFK)活性。因此,NF-κB被所有病毒的癌蛋白诱导。相反,SFK相关信号仅可检测到HVS-C和HVA的癌蛋白。因此,人淋巴细胞的受限转化可能与这些癌蛋白靶向特定的SFK有关。这些结果将使得能够进一步研究与T细胞增殖有关的新型SFK效应子机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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