Muslimov Ilham A, Titmus Margaret, Koenig Edward, Tiedge Henri
Departments of Physiology and Pharmacology and Neurology, State University of New York, Health Science Center at Brooklyn, Brooklyn, New York 11203, USA.
J Neurosci. 2002 Jun 1;22(11):4293-301. doi: 10.1523/JNEUROSCI.22-11-04293.2002.
In neurons, localized RNAs have been identified in dendrites and axons; however, RNA transport in axons remains poorly understood. Here we analyzed axonal RNA transport in goldfish Mauthner neurons in vivo. BC1 RNA, a noncoding RNA polymerase III transcript that is targeted to dendrites in neurons of the rodent nervous system, was used as a probe for axonal RNA transport. Somata of Mauthner neurons were microinjected with various RNAs. Full-length BC1 RNA, but not control RNAs of similar length, was targeted to both axons and dendrites of Mauthner neurons. BC1 RNA was transported in the form of a rapidly advancing wave front that progressed along axons, in a microtubule-dependent manner, at a rate of 2 micrometer/sec. Whereas a BC1 5' segment of 65 nucleotides was transported to axons and dendrites in a way indistinguishable from full-length BC1 RNA, a BC1 3' segment of 60 nucleotides did not enter Mauthner cell processes to any significant extent. In the wake of the wave advancing through the axon, BC1 RNA was found localized to discrete, spatially delimited domains at the axonal surface. Such demarcated cortical concentrations of BC1 RNA could not be observed after disruption of F-actin organization in the axon. It is concluded that the specific delivery of BC1 RNA to spatially defined axonal target sites is a two-step process that requires the sequential participation of microtubules for long-range axial transport and of actin filaments for local radial transfer and focal accumulation in cortical domains.
在神经元中,已在树突和轴突中鉴定出局部RNA;然而,轴突中的RNA运输仍知之甚少。在这里,我们分析了金鱼Mauthner神经元在体内的轴突RNA运输。BC1 RNA是一种非编码RNA聚合酶III转录本,在啮齿动物神经系统的神经元中靶向树突,被用作轴突RNA运输的探针。向Mauthner神经元的胞体显微注射各种RNA。全长BC1 RNA,而不是类似长度的对照RNA,靶向Mauthner神经元的轴突和树突。BC1 RNA以快速推进的波前形式运输,该波前沿轴突以微管依赖的方式以2微米/秒的速度前进。虽然65个核苷酸的BC1 5'片段以与全长BC1 RNA无法区分的方式运输到轴突和树突,但60个核苷酸的BC1 3'片段在很大程度上没有进入Mauthner细胞突起。在波穿过轴突之后,发现BC1 RNA定位于轴突表面离散的、空间界定的区域。在轴突中F-肌动蛋白组织被破坏后,无法观察到这种划定的BC1 RNA皮质浓度。得出的结论是,BC1 RNA向空间定义的轴突靶位点的特异性递送是一个两步过程,该过程需要微管依次参与进行长距离轴向运输,以及肌动蛋白丝参与局部径向转移和在皮质区域的局部积累。