Dabora S L, Sheetz M P
Department of Cell Biology, Washington University Medical School, St. Louis.
Cell Motil Cytoskeleton. 1988;10(4):482-95. doi: 10.1002/cm.970100405.
Directed movements of organelles have been observed in a variety of cultured cells. To study the regulation and molecular basis of intracellular organelle motility, we have prepared extracts from cultured chick embryo fibroblasts (CEF cells) which support the movement of membraneous organelles along microtubules. The velocity, frequency and characteristics of organelle movements in vitro were similar to those within intact cells. Organelles and extract-coated anionic beads moved predominantly (80%) toward the minus ends of microtubules that had been regrown from centrosomes, corresponding to retrograde translocation. Similar microtubule-dependent organelle movements were observed in extracts prepared from other cultured cells (African green monkey kidney and 3T3 cells). Organelle motility was ATP and microtubule dependent. The frequency of organelle movement was inhibited by acidic (pH less than 7) or alkaline (pH greater than 8) solutions, high ionic strength ([ KCl] = 0.1 M), and the chelation of free magnesium ions. Treatment of the extracts with adenylyl imidodiphosphate (AMP-PNP, 7 mM), sodium orthovanadate (vanadate; Na3VO4, 20 microM), or N-ethylmaleimide (NEM, 2 mM) blocked all organelle motility. The decoration of microtubules with organelles was observed in the presence of AMP-PNP or vanadate. Motility was not affected by cytochalasin D (2 microM) or cAMP (1 mM). Kinesin (Mr = 116,000), an anterograde microtubule-based motor, was partially purified from the CEF extract by microtubule affinity purification in the presence of AMP-PNP, and was able to drive the movement of microtubule on glass coverslips. A similar preparation made in the presence of vanadate contained a different subset of proteins and did not support motility. These results demonstrate that intracellular organelle motility can be reproduced in vitro and provide the basis for investigating the roles of individual molecular components involved in the organelle motor complex.
在多种培养细胞中都观察到了细胞器的定向运动。为了研究细胞内细胞器运动的调控及分子基础,我们从培养的鸡胚成纤维细胞(CEF细胞)中制备了提取物,这些提取物能支持膜性细胞器沿微管移动。体外细胞器运动的速度、频率和特征与完整细胞内的相似。细胞器和提取物包被的阴离子珠主要(80%)朝着从中心体重新生长的微管负端移动,这与逆行转运相对应。在从其他培养细胞(非洲绿猴肾细胞和3T3细胞)制备的提取物中也观察到了类似的依赖微管的细胞器运动。细胞器运动依赖于ATP和微管。细胞器运动的频率受到酸性(pH小于7)或碱性(pH大于8)溶液、高离子强度([KCl]=0.1M)以及游离镁离子螯合的抑制。用腺苷酰亚胺二磷酸(AMP-PNP,7mM)、原钒酸钠(钒酸盐;Na3VO4,20μM)或N-乙基马来酰亚胺(NEM,2mM)处理提取物会阻断所有细胞器运动。在存在AMP-PNP或钒酸盐的情况下观察到了细胞器对微管的附着。运动不受细胞松弛素D(2μM)或cAMP(1mM)的影响。驱动蛋白(分子量=116,000)是一种基于微管正向移动的马达蛋白,在存在AMP-PNP的情况下通过微管亲和纯化从CEF提取物中部分纯化出来,并且能够驱动微管在玻璃盖玻片上移动。在存在钒酸盐的情况下进行的类似制备含有不同的蛋白质亚群,并且不支持运动。这些结果表明细胞内细胞器运动可以在体外重现,并为研究参与细胞器马达复合体的各个分子成分的作用提供了基础。