期刊论文详细信息
BMC Cell Biology
Acetylated microtubules are required for fusion of autophagosomes with lysosomes
Research Article
Rui Xie1  Leyuan Liu1  Susan Nguyen1  Wallace L McKeehan1 
[1] Center for Cancer and Stem Cell Biology, Institute of Biosciences and Technology, Texas A&M Health Science Center, 77030-3303, Houston, Texas, USA;
关键词: Paclitaxel;    Vinblastine;    Mitotic Cell;    Nocodazole;    Interphase Cell;   
DOI  :  10.1186/1471-2121-11-89
 received in 2010-04-21, accepted in 2010-11-22,  发布年份 2010
来源: Springer
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【 摘 要 】

BackgroundAutophagy is a dynamic process during which isolation membranes package substrates to form autophagosomes that are fused with lysosomes to form autolysosomes for degradation. Although it is agreed that the LC3II-associated mature autophagosomes move along microtubular tracks, it is still in dispute if the conversion of LC3I to LC3II before autophagosomes are fully mature and subsequent fusion of mature autophagosomes with lysosomes require microtubules.ResultsWe use biochemical markers of autophagy and a collection of microtubule interfering reagents to test the question. Results show that interruption of microtubules with either microtubule stabilizing paclitaxel or destabilizing nocodazole similarly impairs the conversion of LC3I to LC3II, but does not block the degradation of LC3II-associated autophagosomes. Acetylation of microtubules renders them resistant to nocodazole treatment. Treatment with vinblastine that causes depolymerization of both non-acetylated and acetylated microtubules results in impairment of both LC3I-LC3II conversion and LC3II-associated autophagosome fusion with lysosomes.ConclusionsAcetylated microtubules are required for fusion of autophagosomes with lysosomes to form autolysosomes.

【 授权许可】

Unknown   
© Xie et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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