Glycogen Synthase Kinase 3 Inactivation Induces Cell Senescence through Sterol Regulatory Element Binding Protein 1-Mediated Lipogenesis in Chang Cells.
10.3803/EnM.2013.28.4.297
- Author:
You Mie KIM
1
;
Insun SONG
;
Yong Hak SEO
;
Gyesoon YOON
Author Information
1. Department of Biochemistry and Molecular Biology, Ajou University School of Medicine, Suwon, Korea. ypeace@ajou.ac.kr
- Publication Type:Original Article
- Keywords:
Glycogen synthase kinase 3;
Sterol regulatory element binding protein 1;
Lipogenesis;
Cell aging
- MeSH:
Aging*;
Aminophenols;
ATP Citrate (pro-S)-Lyase;
Carrier Proteins*;
Cell Aging;
Deferoxamine;
Fatty Acid Synthetase Complex;
Glycogen Synthase Kinase 3*;
Glycogen Synthase Kinases*;
Glycogen Synthase*;
Glycogen*;
Humans;
Lipogenesis*;
Liver;
Maleimides;
Multienzyme Complexes;
Oxo-Acid-Lyases;
Phosphorylation;
RNA, Small Interfering;
Sterol Regulatory Element Binding Protein 1
- From:Endocrinology and Metabolism
2013;28(4):297-308
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Enhanced lipogenesis plays a critical role in cell senescence via induction of expression of the mature form of sterol regulatory element binding protein 1 (SREBP1), which contributes to an increase in organellar mass, one of the indicators of senescence. We investigated the molecular mechanisms by which signaling molecules control SREBP1-mediated lipogenesis and senescence. METHODS: We developed cellular models for stress-induced senescence, by exposing Chang cells, which are immortalized human liver cells, to subcytotoxic concentrations (200 microM) of deferoxamine (DFO) and H2O2. RESULTS: In this model of stress-induced cell senescence using DFO and H2O2, the phosphorylation profile of glycogen synthase kinase 3alpha (GSK3alpha) and beta corresponded closely to the expression profile of the mature form of SREBP-1 protein. Inhibition of GSK3 with a subcytotoxic concentration of the selective GSK3 inhibitor SB415286 significantly increased mature SREBP1 expression, as well as lipogenesis and organellar mass. In addition, GSK3 inhibition was sufficient to induce senescence in Chang cells. Suppression of GSK3 expression with siRNAs specific to GSK3alpha and beta also increased mature SREBP1 expression and induced senescence. Finally, blocking lipogenesis with fatty acid synthase inhibitors (cerulenin and C75) and siRNA-mediated silencing of SREBP1 and ATP citrate lyase (ACL) significantly attenuated GSK3 inhibition-induced senescence. CONCLUSION: GSK3 inactivation is an important upstream event that induces SREBP1-mediated lipogenesis and consequent cell senescence.
