...
首页> 外文期刊>Journal of cell biology >Delivery of newly synthesized tubulin to rapidly growing distal axons of sympathetic neurons in compartmented cultures.
【24h】

Delivery of newly synthesized tubulin to rapidly growing distal axons of sympathetic neurons in compartmented cultures.

机译:将新合成的微管蛋白输送到间隔培养物中快速生长的交感神经元远端轴突。

获取原文

摘要

Growing axons receive a substantial supply of tubulin and other proteins delivered from sites of synthesis in the cell body by slow axonal transport. To investigate the mechanism of tubulin transport most previous studies have used in vitro models in which the transport of microtubules can be visualized during brief periods of growth. To investigate total tubulin transport in neurons displaying substantial growth over longer periods, we used rat sympathetic neurons in compartmented cultures. Tubulin synthesized during pulses of [35S]methionine was separated from other proteins by immunoprecipitation with monoclonal antibodies to alpha and beta tubulin, further separated on SDS-PAGE, and quantified by phosphorimaging. Results showed that 90% of newly synthesized tubulin moved into the distal axons within 2 d. Furthermore, the leading edge of tubulin was transported at a velocity faster than 4 mm/d, more than four times the rate of axon elongation. This velocity did not diminish with distance from the cell body, suggesting that the transport system is capable of distributing newly synthesized tubulin to growth cones throughout the axonal tree. Neither diffusion nor the an mass transport of axonal microtubules can account for the velocity and magnitude of tubulin transport that was observed. Thus, it is likely that most of the newly synthesized tubulin was supplied to the growing axonal tree in subunit form such as a heterodimer or an oligomer considerably smaller than a microtubule.
机译:生长中的轴突通过缓慢的轴突运输从细胞体内的合成位点获得大量的微管蛋白和其他蛋白质。为了研究微管蛋白的运输机制,大多数先前的研究已经使用了体外模型,在该模型中,可以在生长的短时间内看到微管的运输。为了研究在更长时期内显示出实质性增长的神经元中的总微管蛋白转运,我们在间隔培养物中使用了大鼠交感神经元。在[35S]蛋氨酸脉冲过程中合成的微管蛋白通过用针对α和β微管蛋白的单克隆抗体进行免疫沉淀而与其他蛋白质分离,在SDS-PAGE上进一步分离,并通过磷显像定量。结果显示90%的新合成微管蛋白在2天内移入了远端轴突。此外,微管蛋白的前沿以高于4 mm / d的速度运输,是轴突伸长率的四倍以上。这个速度并没有随着与细胞体距离的增加而减小,这表明运输系统能够将新合成的微管蛋白分布到整个轴突树的生长锥上。轴突微管的扩散或大量运输都不能解释观察到的微管蛋白运输的速度和大小。因此,很可能大部分新合成的微管蛋白都以亚单位形式(例如比微管小得多的异二聚体或低聚物)的形式提供给生长中的轴突树。

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