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E3 泛素连接酶 E6AP 通过下调前脂肪生成因子 C/EBPα 负调控脂肪生成。

E3 ubiquitin ligase E6AP negatively regulates adipogenesis by downregulating proadipogenic factor C/EBPalpha.

机构信息

LSS008, DTDD Division, CSIR-Central Drug Research Institute, Lucknow, India.

出版信息

PLoS One. 2013 Jun 7;8(6):e65330. doi: 10.1371/journal.pone.0065330. Print 2013.

DOI:10.1371/journal.pone.0065330
PMID:23762344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3676453/
Abstract

CCAAT/Enhancer Binding Protein Alpha (C/EBPα) is a key transcription factor involved in the adipocyte differentiation. Here for the first time we demonstrate that E6AP, an E3 ubiquitin ligase inhibits adipocyte differentiation in 3T3-L1 cells as revealed by reduced lipid staining with oil red. Knock down of E6AP in mouse 3T3L1 preadipocytes is sufficient to convert them to adipocytes independent of external hormonal induction. C/EBPα protein level is drastically increased in E6AP deficient 3T3L1 preadipocytes while inverse is observed when wild type E6AP is over expressed. We show that transient transfection of wild type E6AP downregulates C/EBPα protein expression in a dose dependent manner while catalytically inactive E6AP-C843A rather stabilizes it. In addition, wild type E6AP inhibits expression of proadipogenic genes while E6AP-C843A enhances them. More importantly, overexpression of E6AP-C843A in mesenchymal progenitor cells promotes accumulation of lipid droplets while there is drastically reduced lipid droplet formation when E6AP is over expressed. Taken together, our finding suggests that E6AP may negatively control adipogenesis by inhibiting C/EBPα expression by targeting it to ubiquitin-proteasome pathway for degradation.

摘要

CCAAT/增强子结合蛋白α(C/EBPα)是参与脂肪细胞分化的关键转录因子。在这里,我们首次证明 E6AP(一种 E3 泛素连接酶)通过减少油红染色来抑制 3T3-L1 细胞中的脂肪细胞分化。在小鼠 3T3L1 前脂肪细胞中敲低 E6AP 足以使其独立于外部激素诱导转化为脂肪细胞。E6AP 缺陷的 3T3L1 前脂肪细胞中 C/EBPα 蛋白水平明显增加,而当野生型 E6AP 过表达时则相反。我们表明,野生型 E6AP 的瞬时转染以剂量依赖性方式下调 C/EBPα 蛋白表达,而催化失活的 E6AP-C843A 则使其稳定。此外,野生型 E6AP 抑制前脂肪生成基因的表达,而 E6AP-C843A 则增强它们的表达。更重要的是,E6AP-C843A 在间充质祖细胞中的过表达促进脂滴的积累,而当 E6AP 过表达时,脂滴的形成则大大减少。总之,我们的发现表明,E6AP 可能通过将 C/EBPα 靶向泛素-蛋白酶体途径进行降解来负调控脂肪生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/84371a6ac25d/pone.0065330.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/fe9d4d60827b/pone.0065330.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/786a75c3e0ef/pone.0065330.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/46fa1847831e/pone.0065330.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/b48013db9a36/pone.0065330.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/27af3386ad06/pone.0065330.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/84371a6ac25d/pone.0065330.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/fe9d4d60827b/pone.0065330.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/786a75c3e0ef/pone.0065330.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/46fa1847831e/pone.0065330.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/b48013db9a36/pone.0065330.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/27af3386ad06/pone.0065330.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a10/3676453/84371a6ac25d/pone.0065330.g006.jpg

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