Stoothoff Will, Jones Phillip B, Spires-Jones Tara L, Joyner Daniel, Chhabra Ekta, Bercury Kathryn, Fan Zhanyun, Xie Hong, Bacskai Brian, Edd Jon, Irimia Daniel, Hyman Bradley T
MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts 02129, USA.
J Neurochem. 2009 Oct;111(2):417-27. doi: 10.1111/j.1471-4159.2009.06316.x. Epub 2009 Aug 3.
Tau protein is present in six different splice forms in the human brain and interacts with microtubules via either 3 or 4 microtubule binding repeats. An increased ratio of 3 repeat to 4 repeat isoforms is associated with neurodegeneration in inherited forms of frontotemporal dementia. Tau over-expression diminishes axonal transport in several systems, but differential effects of 3 repeat and 4 repeat isoforms have not been studied. We examined the effects of tau on mitochondrial transport and found that both 3 repeat and 4 repeat tau change normal mitochondrial distribution within the cell body and reduce mitochondrial localization to axons; 4 repeat tau has a greater effect than 3 repeat tau. Further, we observed that the 3 repeat and 4 repeat tau cause different alterations in retrograde and anterograde transport dynamics with 3 repeat tau having a slightly stronger effect on axon transport dynamics. Our results indicate that tau-induced changes in axonal transport may be an underlying theme in neurodegenerative diseases associated with isoform specific changes in tau's interaction with microtubules.
Tau蛋白在人类大脑中以六种不同的剪接形式存在,并通过3个或4个微管结合重复序列与微管相互作用。3重复异构体与4重复异构体的比例增加与遗传性额颞叶痴呆的神经退行性变有关。Tau蛋白的过度表达会减少多个系统中的轴突运输,但尚未研究3重复和4重复异构体的差异作用。我们研究了tau对线粒体运输的影响,发现3重复和4重复tau都会改变细胞体内正常的线粒体分布,并减少线粒体在轴突中的定位;4重复tau的影响比3重复tau更大。此外,我们观察到3重复和4重复tau会导致逆行和顺行运输动力学的不同改变,3重复tau对轴突运输动力学的影响稍强。我们的结果表明,tau诱导的轴突运输变化可能是与tau与微管相互作用的异构体特异性变化相关的神经退行性疾病的一个潜在主题。