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一种高分子量非肌肉原肌球蛋白同工型刺激细胞器逆行运输。

A high molecular mass non-muscle tropomyosin isoform stimulates retrograde organelle transport.

作者信息

Pelham R J, Lin J J, Wang Y L

机构信息

Cell Biology Group, Worcester Foundation for Biomedical Research, Shrewsbury, MA 01545, USA.

出版信息

J Cell Sci. 1996 May;109 ( Pt 5):981-9. doi: 10.1242/jcs.109.5.981.

Abstract

Although non-muscle tropomyosins (TM) have been implicated in various cellular functions, such as stabilization of actin filaments and possibly regulation of organelle transport, their physiological role is still poorly understood. We have probed the role of a high molecular mass isoform of human fibroblast TM, hTM3, in regulating organelle transport by microinjecting an excess amount of bacterially-expressed protein into normal rat kidney (NRK) epithelial cells. The microinjection induced the dramatic retrograde translocation of organelles into the perinuclear area. Microinjection of hTM5, a low molecular mass isoform had no effect on organelle distribution. Fluorescent staining indicated that hTM3 injection stimulated the retrograde movement of both mitochondria and lysosomes. Moreover, both myosin I and cytoplasmic dynein were found to redistribute with the translocated organelles to the perinuclear area, indicating that these organelles were able to move along both microtubules and actin filaments. The involvement of microtubules was further suggested by the partial inhibition of hTM3-induced organelle movement by the microtubule-depolymerizing drug nocodazole. Our results, along with previous genetic and antibody microinjection studies, suggest that hTM3 may be involved in the regulation of organelle transport.

摘要

尽管非肌肉型原肌球蛋白(TM)参与了多种细胞功能,如肌动蛋白丝的稳定以及可能对细胞器运输的调节,但其生理作用仍知之甚少。我们通过向正常大鼠肾(NRK)上皮细胞显微注射过量细菌表达的蛋白,探究了人成纤维细胞TM的一种高分子量异构体hTM3在调节细胞器运输中的作用。显微注射导致细胞器向核周区域发生显著的逆行转运。注射低分子量异构体hTM5对细胞器分布没有影响。荧光染色表明,注射hTM3刺激了线粒体和溶酶体的逆行运动。此外,发现肌球蛋白I和胞质动力蛋白都随着转运的细胞器重新分布到核周区域,这表明这些细胞器能够沿着微管和肌动蛋白丝移动。微管解聚药物诺考达唑对hTM3诱导的细胞器运动有部分抑制作用,这进一步表明微管参与其中。我们的结果,连同先前的基因和抗体显微注射研究,表明hTM3可能参与细胞器运输的调节。

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