Nadar Vidya C, Ketschek Andrea, Myers Kenneth A, Gallo Gianluca, Baas Peter W
Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA 19129, USA.
Curr Biol. 2008 Dec 23;18(24):1972-7. doi: 10.1016/j.cub.2008.11.021. Epub 2008 Dec 11.
Inhibition of kinesin-5, a mitotic motor protein also expressed in neurons, causes axons to grow faster as a result of alterations in the forces on microtubules (MTs) in the axonal shaft. Here, we investigate whether kinesin-5 plays a role in growth-cone guidance. Growth-cone turning requires that MTs in the central (C-) domain enter the peripheral (P-) domain in the direction of the turn. We found that inhibition of kinesin-5 in cultured neurons prevents MTs from polarizing within growth cones and causes them to grow past cues that would normally cause them to turn. We found that kinesin-5 is enriched in the transition (T-) zone of the growth cone and that kinesin-5 is preferentially phosphorylated on the side opposite the invasion of MTs. Moreover, when a growth cone encounters a turning cue, phospho-kinesin-5 polarizes even before the growth cone turns. Additional studies indicate that kinesin-5 works in part by antagonizing cytoplasmic dynein and that these motor-driven forces function together with the dynamic properties of the MTs to determine whether MTs can enter the P-domain. We propose that kinesin-5 permits MTs to selectively invade one side of the growth cone by opposing their entry into the other side.
驱动蛋白-5是一种在神经元中也有表达的有丝分裂运动蛋白,抑制它会导致轴突因轴突干中微管(MT)受力改变而生长加快。在此,我们研究驱动蛋白-5在生长锥导向中是否发挥作用。生长锥转向要求中央(C-)结构域中的微管朝着转向方向进入外周(P-)结构域。我们发现,在培养的神经元中抑制驱动蛋白-5会阻止微管在生长锥内极化,并使它们生长越过通常会导致它们转向的信号。我们发现驱动蛋白-5在生长锥的过渡(T-)区富集,并且驱动蛋白-5在微管侵入相反一侧优先发生磷酸化。此外,当生长锥遇到转向信号时,磷酸化的驱动蛋白-5甚至在生长锥转向之前就发生极化。进一步的研究表明,驱动蛋白-5部分通过拮抗胞质动力蛋白发挥作用,并且这些由运动蛋白驱动的力与微管的动态特性共同作用,以确定微管是否能够进入P结构域。我们提出,驱动蛋白-5通过阻止微管进入生长锥的另一侧,使微管能够选择性地侵入生长锥的一侧。