Trinczek B, Ebneth A, Mandelkow E M, Mandelkow E
Max-Planck Unit for Structural Molecular Biology, Notkestrasse 85, D-22607 Hamburg, Germany.
J Cell Sci. 1999 Jul;112 ( Pt 14):2355-67. doi: 10.1242/jcs.112.14.2355.
We have performed a real time analysis of fluorescence-tagged vesicle and mitochondria movement in living CHO cells transfected with microtubule-associated protein tau or its microtubule-binding domain. tau does not alter the speed of moving vesicles, but it affects the frequencies of attachment and detachment to the microtubule tracks. Thus, tau decreases the run lengths both for plus-end and minus-end directed motion to an equal extent. Reversals from minus-end to plus-end directed movement of single vesicles are strongly reduced by tau, but reversals in the opposite direction (plus to minus) are not. Analogous effects are observed with the transport of mitochondria and even with that of vimentin intermediate filaments. The net effect is a directional bias in the minus-end direction of microtubules which leads to the retraction of mitochondria or vimentin IFs towards the cell center. The data suggest that tau can control intracellular trafficking by affecting the attachment and detachment cycle of the motors, in particular by reducing the attachment of kinesin to microtubules, whereas the movement itself is unaffected.
我们对转染了微管相关蛋白tau或其微管结合结构域的活CHO细胞中荧光标记的囊泡和线粒体运动进行了实时分析。tau不会改变移动囊泡的速度,但会影响其与微管轨道的附着和脱离频率。因此,tau会同等程度地缩短正向和负向运动的行程长度。tau会强烈减少单个囊泡从负向到正向运动的反转,但不会减少相反方向(正向到负向)的反转。在线粒体运输甚至波形蛋白中间丝运输中也观察到了类似的效应。最终结果是微管负向方向出现定向偏差,导致线粒体或波形蛋白中间丝向细胞中心回缩。数据表明,tau可以通过影响马达的附着和脱离循环来控制细胞内运输,特别是通过减少驱动蛋白与微管的附着,而运动本身不受影响。