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本文引用的文献

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The E3 ubiquitin ligase NEDD4 negatively regulates HER3/ErbB3 level and signaling.E3 泛素连接酶 NEDD4 负调控 HER3/ErbB3 水平和信号转导。
Oncogene. 2015 Feb 26;34(9):1105-15. doi: 10.1038/onc.2014.56. Epub 2014 Mar 24.
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SCF(β-TRCP)-mediated degradation of NEDD4 inhibits tumorigenesis through modulating the PTEN/Akt signaling pathway.SCF(β-TRCP)介导的NEDD4降解通过调节PTEN/Akt信号通路抑制肿瘤发生。
Oncotarget. 2014 Feb 28;5(4):1026-37. doi: 10.18632/oncotarget.1675.
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Regulation of mTORC1 and its impact on gene expression at a glance.mTORC1 的调控及其对基因表达的影响一览
J Cell Sci. 2013 Apr 15;126(Pt 8):1713-9. doi: 10.1242/jcs.125773. Epub 2013 May 2.
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mTOR inhibits autophagy by controlling ULK1 ubiquitylation, self-association and function through AMBRA1 and TRAF6.mTOR 通过控制 ULK1 的泛素化、自聚集和功能,通过 AMBRA1 和 TRAF6 来抑制自噬。
Nat Cell Biol. 2013 Apr;15(4):406-16. doi: 10.1038/ncb2708. Epub 2013 Mar 24.
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NEDD4 is overexpressed in colorectal cancer and promotes colonic cell growth independently of the PI3K/PTEN/AKT pathway.NEDD4 在结直肠癌中过表达,并独立于 PI3K/PTEN/AKT 通路促进结肠细胞生长。
Cell Signal. 2013 Jan;25(1):12-8. doi: 10.1016/j.cellsig.2012.08.012. Epub 2012 Sep 5.
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mTOR signaling in growth control and disease.mTOR 信号在生长控制和疾病中的作用。
Cell. 2012 Apr 13;149(2):274-93. doi: 10.1016/j.cell.2012.03.017.
7
Nedd4-1 binds and ubiquitylates activated FGFR1 to control its endocytosis and function.Nedd4-1 结合并泛素化激活的 FGFR1,以控制其内化和功能。
EMBO J. 2011 Jul 15;30(16):3259-73. doi: 10.1038/emboj.2011.234.
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Autophagy and metabolism.自噬和代谢。
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mTOR regulation of autophagy.mTOR 对自噬的调控。
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mTOR signaling at a glance.mTOR信号通路概述。
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Nedd4 E3泛素连接酶促进细胞增殖和自噬。

Nedd4 E3 ubiquitin ligase promotes cell proliferation and autophagy.

作者信息

Li Yuyin, Zhang Li, Zhou Jie, Luo Shenheng, Huang Rui, Zhao Changcai, Diao Aipo

机构信息

School of Biotechnology, Tianjin University of Science and Technology, Key Lab of Industrial Fermentation Microbiology of the Ministry of Education, Tianjin, 300457, China.

出版信息

Cell Prolif. 2015 Jun;48(3):338-47. doi: 10.1111/cpr.12184. Epub 2015 Mar 24.

DOI:10.1111/cpr.12184
PMID:25809873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6495840/
Abstract

OBJECTIVES

Nedd4 (neural precursor cell expressed developmentally down-regulated protein 4) is a member of the HECT E3 ubiquitin ligases, and is elevated in prostate, bladder and colorectal cancers, and promotes colonic cell population expansion. Up to now, molecular mechanisms of how Nedd4 functions, have not been well understood.

MATERIALS AND METHODS

In this study, shRNA was used to reduce expression of Nedd4 in the human prostate carcinoma cell line DU145. To analyse effects of Nedd4 on cell proliferation, MTT and colony formation assays were performed. DAPI staining and FACS analysis were used to investigate outcomes of Nedd4 activity, on apoptosis. Results of Nedd4 expression on lysosomal membrane permeabilization and autophagy were further investigated using acridine orange (AO) staining, immunofluorescence and western blot analysis.

RESULTS

We found that in HeLa cells, expression of Nedd4 promoted cell proliferation, whereas its knockdown inhibited colony formation and induced apoptosis in DU145 cells. Furthermore, down-regulation of Nedd4 in DU145 cells promoted lysosomal membrane permeabilization. We also found that down-regulation of Nedd4 inhibited autophagy in both DU145 and A549 cells. Investigation into mechanisms involved revealed that knockdown of endogenous Nedd4 expression notably increased activated mTOR (p-mTOR) levels, which suggests that mTOR signalling was involved in the Nedd4-mediated autophagy.

CONCLUSIONS

Our results indicate that expression of Nedd4 promoted cell proliferation and colony formation but prevented apoptosis. Moreover, Nedd4 promoted autophagy and was associated with the mTOR signalling pathway.

摘要

目的

Nedd4(神经前体细胞表达的发育下调蛋白4)是HECT E3泛素连接酶家族的成员,在前列腺癌、膀胱癌和结直肠癌中表达升高,并促进结肠细胞群体扩张。到目前为止,Nedd4发挥作用的分子机制尚未完全清楚。

材料与方法

在本研究中,使用短发夹RNA(shRNA)降低人前列腺癌细胞系DU145中Nedd4的表达。为了分析Nedd4对细胞增殖的影响,进行了MTT和集落形成实验。采用4',6-二脒基-2-苯基吲哚(DAPI)染色和荧光激活细胞分选(FACS)分析来研究Nedd4活性对细胞凋亡的影响。使用吖啶橙(AO)染色、免疫荧光和蛋白质印迹分析进一步研究Nedd4表达对溶酶体膜通透性和自噬的影响。

结果

我们发现,在HeLa细胞中,Nedd4的表达促进细胞增殖,而其敲低则抑制DU145细胞的集落形成并诱导细胞凋亡。此外,DU145细胞中Nedd4的下调促进了溶酶体膜通透性。我们还发现,Nedd4的下调在DU145和A549细胞中均抑制自噬。对相关机制的研究表明,内源性Nedd4表达的敲低显著增加了激活的哺乳动物雷帕霉素靶蛋白(p-mTOR)水平,这表明mTOR信号通路参与了Nedd4介导的自噬。

结论

我们的结果表明,Nedd4的表达促进细胞增殖和集落形成,但抑制细胞凋亡。此外,Nedd4促进自噬并与mTOR信号通路相关。