Premium
Methyl gallate, a potent antioxidant inhibits mouse and human adipocyte differentiation and oxidative stress in adipocytes through impairment of mitotic clonal expansion
Author(s) -
Rahman Naimur,
Jeon Miso,
Kim YongSik
Publication year - 2016
Publication title -
biofactors
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.204
H-Index - 94
eISSN - 1872-8081
pISSN - 0951-6433
DOI - 10.1002/biof.1310
Subject(s) - adipogenesis , oxidative stress , microbiology and biotechnology , transcription factor , e2f1 , cyclin dependent kinase 2 , chemistry , cyclin a , cyclin e , phosphorylation , cyclin , retinoic acid , biology , cell cycle , biochemistry , protein kinase a , cell , mesenchymal stem cell , gene
Methyl gallate (MG) is a derivative of gallic acid and a potent antioxidant. In this study, we confirmed that MG treatment effectively inhibits lipid accumulation, which occurred mostly in the early stages of adipogenesis. We also showed that shortly after adipogenic induction, MG facilitated a G0/G1 cell cycle arrest. Mechanistic studies revealed that MG treatment inhibited ERK1/2 phosphorylation, which is a key regulator of the G1‐ to S‐phase transition. Furthermore, MG treatment prevented the adipogenic hormonal stimuli‐induced inhibition of the cyclin‐dependent kinase inhibitor p27 Kip1 . This led to inhibition of the transcription factor E2F1 by preventing the phosphorylation of, and thereby activation of its destruction partner RB. MG treatment also downregulated factors that are upstream of RB‐E2F1 signaling such as Cdk2, Cyclin E, Cdk4, and Cyclin D1 where Cyclin D3 level was unaffected. We also found that MG treatment markedly decreased the expression and phosphorylation of C/EBPβ, by phosphorylating, and therefore inactivating, GSK3β, which is a prerequisite for its DNA binding capacity, and thereby mitotic clonal expansion (MCE). Ultimately, MG treatment downregulates key terminal adipogenic transcription factors including C/EBPα, PPARγ , aP2 ( Fabp4), and adiponectin . Moreover, MG also protects adipocytes from oxidative stress by alleviating intracellular reactive oxygen species and activating Nrf2, HO‐1, and PRDX3. Thus, this study provides a mechanistic insight into the anti‐adipogenic actions of MG. © 2016 BioFactors, 42(6):716–726, 2016