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轴突的活力和线粒体功能依赖于交感神经元中的局部蛋白质合成。

Axon viability and mitochondrial function are dependent on local protein synthesis in sympathetic neurons.

作者信息

Hillefors Mi, Gioio Anthony E, Mameza Marie G, Kaplan Barry B

机构信息

Laboratory of Molecular Biology, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892-1381, USA.

出版信息

Cell Mol Neurobiol. 2007 Sep;27(6):701-16. doi: 10.1007/s10571-007-9148-y. Epub 2007 Jul 6.

Abstract

(1) Axons contain numerous mRNAs and a local protein synthetic system that can be regulated independently of the cell body. (2) In this study, cultured primary sympathetic neurons were employed, to assess the effect of local protein synthesis blockade on axon viability and mitochondrial function. (3) Inhibition of local protein synthesis reduced newly synthesized axonal proteins by 65% and resulted in axon retraction after 6 h. Acute inhibition of local protein synthesis also resulted in a significant decrease in the membrane potential of axonal mitochondria. Likewise, blockade of local protein transport into the mitochondria by transfection of the axons with Hsp90 C-terminal domain decreased the mitochondrial membrane potential by 65%. Moreover, inhibition of the local protein synthetic system also reduced the ability of mitochondria to restore axonal levels of ATP after KCl-induced depolarization. (4) Taken together, these results indicate that the local protein synthetic system plays an important role in mitochondrial function and the maintenance of the axon.

摘要

(1)轴突含有大量信使核糖核酸(mRNAs)和一个可独立于细胞体进行调控的局部蛋白质合成系统。(2)在本研究中,使用原代培养的交感神经元来评估局部蛋白质合成阻断对轴突活力和线粒体功能的影响。(3)局部蛋白质合成的抑制使新合成的轴突蛋白减少了65%,并在6小时后导致轴突回缩。局部蛋白质合成的急性抑制还导致轴突线粒体膜电位显著下降。同样,通过用热休克蛋白90(Hsp90)C末端结构域转染轴突来阻断局部蛋白质向线粒体的转运,使线粒体膜电位降低了65%。此外,局部蛋白质合成系统的抑制还降低了线粒体在氯化钾(KCl)诱导的去极化后恢复轴突三磷酸腺苷(ATP)水平的能力。(4)综上所述,这些结果表明局部蛋白质合成系统在维持线粒体功能和轴突方面发挥着重要作用。

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