首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Differences in modifications of cytoplasmic free Ca2+ concentration and 86Rb+ influx in human neoplastic B cells by antibodies to mu- relative to delta-Ig heavy chains.
【2h】

Differences in modifications of cytoplasmic free Ca2+ concentration and 86Rb+ influx in human neoplastic B cells by antibodies to mu- relative to delta-Ig heavy chains.

机译:相对于δ-Ig重链的抗体对人肿瘤B细胞中胞质游离Ca2 +浓度和86Rb +内流的修饰差异。

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

Cytoplasmic free Ca2+ concentration and influx of 86Rb+ (K+ analogue) were determined during the first minutes after stimulation of neoplastic human B cells and B cell lines by antibodies to surface Ig. The Ca2+ concentration increased in the great majority of samples (41 of 48). All of four B cell lines also responded, providing formal evidence that accessory cells are not required for this early, surface Ig-mediated event. Antibodies to delta as well as mu, heavy chains (anti-delta and anti-mu) could induce both Ca2+ and 86Rb+ responses. 86Rb+ responders were found within the group of Ca2+ responders, but no quantitative relation was observed between the two responses. In cells expressing both sIgM and sIgD, antibodies to delta heavy chains were more potent than those to mu heavy chains in inducing Ca2+ responses, whereas the opposite pattern was seen with regard to 86Rb+ responses. These results demonstrate that sIgM and sIgD can deliver different biochemical signals to the cell.
机译:在通过表面Ig抗体刺激赘生性人B细胞和B细胞系后的第一分钟内,确定了细胞质的游离Ca2 +浓度和86Rb +(K +类似物)的流入。大多数样品中的Ca2 +浓度增加(48个样品中的41个)。所有四个B细胞系也都做出了反应,从而提供了正式证据,表明这种早期的表面Ig介导的事件不需要辅助细胞。针对δ以及mu,重链的抗体(反delta和anti-mu)可以诱导Ca2 +和86Rb +反应。在Ca2 +响应者组中发现了86Rb +响应者,但在两种响应之间未发现定量关系。在同时表达sIgM和sIgD的细胞中,针对δ重链的抗体在诱导Ca2 +应答方面比针对mu重链的抗体更有效,而对于86Rb +应答,则观察到相反的模式。这些结果表明,sIgM和sIgD可以向细胞传递不同的生化信号。

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