Hollenbeck P J, Bray D
Cell Biophysics Unit, Medical Research Council, London, England.
J Cell Biol. 1987 Dec;105(6 Pt 1):2827-35. doi: 10.1083/jcb.105.6.2827.
We have examined the movements, composition, and cellular origin of phase-dense varicosities in cultures of chick sympathetic and sensory neurons. These organelles are variable in diameter (typically between 0.2 and 2 microns) and undergo saltatory movements both towards and away from the neuronal cell body. Their mean velocities vary inversely with the size of the organelle and are greater in the retrograde than the anterograde direction. Organelles stain with the lipophilic dye 1, 1'-dioctadecyl-3,3,3',3'-tetramethyl-indocarbocyanine and with antibodies to cytoskeletal components. In cultures double-stained with antibodies to alpha-tubulin and 70-kD neurofilament protein (NF-L), approximately 40% of the organelles stain for tubulin, 30% stain for NF-L, 10% stain for both tubulin and NF-L, and 40% show no staining with either antibody. The association of cytoskeletal proteins with the organelles shows that these proteins are able to move by a form of rapid axonal transport. Under most culture conditions the predominant direction of movement is towards the cell body, suggesting that the organelles are produced at or near the growth cone. Retrograde movements continue in culture medium lacking protein or high molecular mass components and increase under conditions in which the advance of the growth cone is arrested. There is a fourfold increase in the number of organelles moving retrogradely in neurites that encounter a substratum-associated barrier to elongation; retrograde movements increase similarly in cultures exposed to cytochalasin at levels known to block growth cone advance. No previously described organelle shows behavior coordinated with axonal growth in this way. We propose that the organelles contain membrane and cytoskeletal components that have been delivered to the growth cone, by slow or fast anterograde transport, in excess of the amounts required to synthesize more axon. In view of their rapid mobility and variable contents, we suggest that they be called "neuronal parcels."
我们研究了鸡交感神经元和感觉神经元培养物中相致密曲张体的运动、组成及细胞起源。这些细胞器直径各异(通常在0.2至2微米之间),并朝着和远离神经元细胞体进行跳跃式运动。它们的平均速度与细胞器大小成反比,逆行方向的速度大于顺行方向。细胞器能用亲脂性染料1,1'-二辛基-3,3,3',3'-四甲基吲哚羰花青以及针对细胞骨架成分的抗体进行染色。在用抗α-微管蛋白和70-kD神经丝蛋白(NF-L)抗体进行双重染色的培养物中,约40%的细胞器对微管蛋白染色,30%对NF-L染色,10%对微管蛋白和NF-L都染色,40%对两种抗体均无染色。细胞骨架蛋白与细胞器的关联表明这些蛋白能够通过一种快速轴突运输形式移动。在大多数培养条件下,运动的主要方向是朝向细胞体,这表明细胞器是在生长锥处或其附近产生的。在缺乏蛋白质或高分子量成分的培养基中,逆行运动仍会继续,并且在生长锥前进受阻的条件下会增加。在遇到与基质相关的伸长障碍的神经突中,逆行运动的细胞器数量增加了四倍;在暴露于已知能阻止生长锥前进水平的细胞松弛素的培养物中,逆行运动也有类似增加。此前没有描述过的细胞器以这种方式表现出与轴突生长协调的行为。我们提出,这些细胞器包含通过慢速或快速顺行运输递送至生长锥的膜和细胞骨架成分,其数量超过合成更多轴突所需的量。鉴于它们的快速移动性和可变内容物,我们建议将它们称为“神经元包裹”。