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III 型中间丝波形蛋白调节细胞器分布并调节自噬。

The type III intermediate filament vimentin regulates organelle distribution and modulates autophagy.

机构信息

School of Applied Sciences, Edinburgh Napier University, Sighthill Campus, Sighthill Court, Edinburgh, United Kingdom.

Centre for Genomic & Experimental Medicine, University of Edinburgh, Western General Hospital Campus, Crewe Road, Edinburgh, United Kingdom.

出版信息

PLoS One. 2019 Jan 30;14(1):e0209665. doi: 10.1371/journal.pone.0209665. eCollection 2019.

Abstract

The cytoskeletal protein vimentin plays a key role in positioning of organelles within the cytosol and has been linked to the regulation of numerous cellular processes including autophagy, however, how vimentin regulates autophagy remains relatively unexplored. Here we report that inhibition of vimentin using the steroidal lactone Withaferin A (WFA) causes vimentin to aggregate, and this is associated with the relocalisation of organelles including autophagosomes and lysosomes from the cytosol to a juxtanuclear location. Vimentin inhibition causes autophagosomes to accumulate, and we demonstrate this results from modulation of mechanistic target of rapamycin (mTORC1) activity, and disruption of autophagosome-lysosome fusion. We suggest that vimentin plays a physiological role in autophagosome and lysosome positioning, thus identifying vimentin as a key factor in the regulation of mTORC1 and autophagy.

摘要

细胞骨架蛋白波形蛋白在细胞器在细胞质中的定位中起着关键作用,并且与包括自噬在内的许多细胞过程的调节有关,然而,波形蛋白如何调节自噬仍然相对未知。在这里,我们报告说,使用甾体内酯 Withaferin A(WFA)抑制波形蛋白会导致波形蛋白聚集,这与细胞器的重定位有关,包括自噬体和溶酶体从细胞质到核周位置。波形蛋白抑制导致自噬体积累,我们证明这是由于机械性靶标雷帕霉素(mTORC1)活性的调节以及自噬体-溶酶体融合的破坏所致。我们认为波形蛋白在自噬体和溶酶体定位中发挥生理作用,因此将波形蛋白鉴定为调节 mTORC1 和自噬的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1487/6353089/6b58029313c1/pone.0209665.g001.jpg

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