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哺乳动物细胞中基于微管的细胞周期依赖性细胞质动力蛋白的动态运输。

Cell cycle-dependent microtubule-based dynamic transport of cytoplasmic dynein in mammalian cells.

机构信息

Department of Pharmacology, Juntendo University School of Medicine, Tokyo, Japan.

出版信息

PLoS One. 2009 Nov 13;4(11):e7827. doi: 10.1371/journal.pone.0007827.

DOI:10.1371/journal.pone.0007827
PMID:19915671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2772020/
Abstract

BACKGROUND

Cytoplasmic dynein complex is a large multi-subunit microtubule (MT)-associated molecular motor involved in various cellular functions including organelle positioning, vesicle transport and cell division. However, regulatory mechanism of the cell-cycle dependent distribution of dynein has not fully been understood.

METHODOLOGY/PRINCIPAL FINDINGS: Here we report live-cell imaging of cytoplasmic dynein in HeLa cells, by expressing multifunctional green fluorescent protein (mfGFP)-tagged 74-kDa intermediate chain (IC74). IC74-mfGFP was successfully incorporated into functional dynein complex. In interphase, dynein moved bi-directionally along with MTs, which might carry cargos such as transport vesicles. A substantial fraction of dynein moved toward cell periphery together with EB1, a member of MT plus end-tracking proteins (+TIPs), suggesting +TIPs-mediated transport of dynein. In late-interphase and prophase, dynein was localized at the centrosomes and the radial MT array. In prometaphase and metaphase, dynein was localized at spindle MTs where it frequently moved from spindle poles toward chromosomes or cell cortex. +TIPs may be involved in the transport of spindle dyneins. Possible kinetochore and cortical dyneins were also observed.

CONCLUSIONS AND SIGNIFICANCE

These findings suggest that cytoplasmic dynein is transported to the site of action in preparation for the following cellular events, primarily by the MT-based transport. The MT-based transport may have greater advantage than simple diffusion of soluble dynein in rapid and efficient transport of the limited concentration of the protein.

摘要

背景

细胞质动力蛋白复合物是一种大型多亚基微管(MT)相关分子马达,参与多种细胞功能,包括细胞器定位、囊泡运输和细胞分裂。然而,细胞周期依赖性动力蛋白分布的调节机制尚未完全理解。

方法/主要发现:在这里,我们通过表达多功能绿色荧光蛋白(mfGFP)标记的 74-kDa 中间链(IC74),报告了 HeLa 细胞中细胞质动力蛋白的活细胞成像。IC74-mfGFP 成功地掺入到功能性动力蛋白复合物中。在间期,动力蛋白沿 MT 双向移动,可能携带运输囊泡等货物。相当一部分动力蛋白与 EB1(MT 加端追踪蛋白(+TIPs)的成员)一起向细胞边缘移动,这表明动力蛋白的+TIPs 介导的运输。在晚期间期和前期,动力蛋白定位于中心体和放射状 MT 阵列。在前期和中期,动力蛋白定位于纺锤体 MT 上,它经常从纺锤体极向染色体或细胞皮层移动。+TIPs 可能参与纺锤体动力蛋白的运输。还观察到可能的动粒和皮质动力蛋白。

结论和意义

这些发现表明,细胞质动力蛋白通过基于 MT 的运输被运输到作用部位,为随后的细胞事件做准备。与可溶性动力蛋白的简单扩散相比,基于 MT 的运输在快速和有效地运输有限浓度的蛋白质方面具有更大的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/da4dfe2f9609/pone.0007827.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/63f9945bce93/pone.0007827.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/525dd33de1a6/pone.0007827.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/cc42fe52f145/pone.0007827.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/ddc84aeb4a69/pone.0007827.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/725e2ebfef17/pone.0007827.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/24f8bc35e97a/pone.0007827.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/da4dfe2f9609/pone.0007827.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/63f9945bce93/pone.0007827.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/69bf3a38af41/pone.0007827.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/525dd33de1a6/pone.0007827.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/cc42fe52f145/pone.0007827.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/ddc84aeb4a69/pone.0007827.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/725e2ebfef17/pone.0007827.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/24f8bc35e97a/pone.0007827.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c053/2772020/da4dfe2f9609/pone.0007827.g008.jpg

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