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Capping and mitogenesis: A model implicating microfilaments in lymphocyte activation

机译:封端和促进剂:一种暗集淋巴细胞活化中微通丝的模型

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摘要

In lymphocytes cap formation induced by concanavalin A (con A) was found to be concentration dependent on the mitogen in the presence of colchicine, a microtubule disrupting agent. The dose-respone of cap formation under these conditions was similar to mitogen dose-response. In addition, a direct correlation was found between con A capping induced in the presence of colchicine and mitogenic responses with con A alone. Agents such as dibutyryl cyclic AMP, which suppress mitogenic responses, decrease capping. Zinc increases capping when it causes enhancement of mitogenesis and decreases capping when it suppresses mitogenic response. These observations are interpreted on the basis of a model in which binding of con A to surface receptors leads to formation of microfilaments, which might be essential for capping as well as the initiation of DNA synthesis. Thus, the experimental observations in this report lend support to a model implicating the formation of microfilaments as a crucial event in triggering a variety of cellular responses following ligand binding.
机译:在淋巴细胞帽中被诱导诱导(CON A)诱导的胶质形成浓度依赖于莫尔氏菌,溶解剂中的微管破坏剂。这些条件下帽形成的剂量respone类似于丝分裂剂剂量反应。此外,在Con Conclicine和单独的锥形响应存在下诱导的封端之间发现直接相关性。抑制促致致态反应的二丁酰基循环放大器等药剂减少封端。锌会增加封端,导致促进促进剂量并减少介质致致致态响应时降低封端。这些观察结果被解释为基于该模型,其中CON A与表面受体的结合导致形成微丝,这可能是封端的必要条件以及DNA合成的开始。因此,本报告中的实验观察借助于暗集形成微丝的模型作为触发配体结合后触发各种细胞反应的关键事件。

著录项

  • 作者

    K. Murali Krishna Rao;

  • 作者单位
  • 年度 1982
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  • 原文格式 PDF
  • 正文语种 en_us
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