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抑制动力蛋白而非驱动蛋白会导致轴突神经突内神经丝异常局灶性积聚。

Inhibition of dynein but not kinesin induces aberrant focal accumulation of neurofilaments within axonal neurites.

作者信息

Motil Jennifer, Dubey Maya, Chan Walter K-H, Shea Thomas B

机构信息

Center for Cellular Neurobiology and Neurodegeneration Research, Department of Biological Sciences, University of Massachusetts Lowell, One University Avenue, Lowell, MA 01854, USA.

出版信息

Brain Res. 2007 Aug 20;1164:125-31. doi: 10.1016/j.brainres.2006.09.108. Epub 2007 Jul 20.

Abstract

Studies from several laboratories indicate that the microtubule motors kinesin and dynein respectively participate in anterograde and retrograde axonal transport of neurofilaments. Inhibition of dynein function by transfection with a construct expressing dynamitin or intracellular delivery of anti-dynein antibodies accelerates anterograde transport, which has been interpreted to indicate that the opposing action of both motors mediates the normal distribution of neurofilaments along axons. Herein, we demonstrate that, while expression of relatively low levels of exogenous dynamitin indeed accelerated anterograde neurofilament transport along axonal neurites in culture, expression of progressively increasing levels of dynamitin induced focal accumulation of neurofilaments within axonal neurites and eventually caused neurite retraction. Inhibition of kinesin inhibited anterograde transport, but did not induce similar focal accumulations. These findings are consistent with studies indicating that perturbations in dynein activity can contribute to the aberrant accumulations of neurofilaments that accompany ALS/motor neuron disease.

摘要

来自多个实验室的研究表明,微管马达驱动蛋白和动力蛋白分别参与神经丝的顺行和逆行轴突运输。通过转染表达动力蛋白结合蛋白的构建体或在细胞内递送抗动力蛋白抗体来抑制动力蛋白功能,可加速顺行运输,这被解释为表明两种马达的相反作用介导了神经丝沿轴突的正常分布。在此,我们证明,虽然表达相对低水平的外源性动力蛋白结合蛋白确实加速了培养的轴突神经突中神经丝的顺行运输,但随着动力蛋白结合蛋白表达水平的逐渐增加,会诱导神经丝在轴突神经突内局部积聚,并最终导致神经突回缩。抑制驱动蛋白会抑制顺行运输,但不会诱导类似的局部积聚。这些发现与表明动力蛋白活性紊乱可能导致与肌萎缩侧索硬化症/运动神经元疾病相关的神经丝异常积聚的研究一致。

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