首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >PARTICLES MOVE ALONG ACTIN FILAMENT BUNDLES IN NERVE GROWTH CONES
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PARTICLES MOVE ALONG ACTIN FILAMENT BUNDLES IN NERVE GROWTH CONES

机译:颗粒在神经生长锥中沿着肌动蛋白丝束移动

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Organelle movement along actin filaments has been demonstrated in dissociated squid axoplasm [Kurznetsov, S.A., Langford, G.M. & Weiss, D.G. (1992) Nature (London) 356, 722-725 and Bearer, E.L., DeGiorgis, J.A., Bodner, R.A., Rao, A.W. & Reese, T.S. (1993) Proc. Natl. Acad. Sci. USA 90, 11252-11256] but has not been shown to occur in intact neurons, Here we demonstrate that intracellular transport occurs along actin filament bundles in intact neuronal growth cones. We used video-enhanced differential interference contrast microscopy to observe intracellular transport in superior cervical ganglion neurons cultured under conditions that enhance the visibility of actin bundles within growth cone lamellipodia. Intracellular particles, ranging in size from <0.5-1.5 mu m, moved along linear structures (termed transport bundles) at an average maximum rate of 0.48 mu m/sec. After particle movement had been viewed, cultures were preserved by rapid perfusion with chemical fixative, To determine whether particle transport occurred along actin, we then used fluorescence microscopy to correlate this movement with actin and microtubule distributions in the same growth cones, The observed transport bundles colocalized with actin but not with microtubules. The rates of particle movement and the association of moving particles with actin filament bundles suggest that myosins may participate in the transport of organelles (or other materials) in intact neurons. [References: 15]
机译:在解离的鱿鱼轴质中已经证明了沿着肌动蛋白丝的细胞器运动[Kurznetsov,S.A.,Langford,G.M. &Weiss,D.G. (1992)Nature(London)356,722-725和Bearer,E.L.,DeGiorgis,J.A.,Bodner,R.A.,Rao,A.W.和T.S. Reese (1993)美国国家科学院院刊。 Natl。学院科学USA 90,11252-11256],但尚未证明它在完整的神经元中发生。在这里,我们证明细胞内转运是沿着完整神经元生长锥中的肌动蛋白丝束发生的。我们使用视频增强的差分干涉对比显微镜观察了在可增强肌动蛋白束在生长锥片状脂膜内的可见性的条件下培养的上颈神经节神经元的细胞内转运。尺寸在<0.5-1.5微米之间的细胞内颗粒沿着线性结构(称为运输束)移动,平均最大速率为0.48微米/秒。在观察到颗粒的运动后,通过化学固定剂的快速灌注来保存培养物。为了确定颗粒是否沿着肌动蛋白运输,我们使用荧光显微镜将这种运动与肌动蛋白和微管在同一生长锥中的分布相关联,观察到的运输束与肌动蛋白共定位,但与微管共定位。颗粒运动的速率以及运动的颗粒与肌动蛋白丝束的关联表明,肌球蛋白可能参与完整神经元中细胞器(或其他物质)的运输。 [参考:15]

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