Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8399632 | Mitochondrion | 2014 | 10 Pages |
Abstract
Mitochondrial biogenesis, a mitochondrial growth and division process, is crucial for adaptation to metabolic stress. The present study demonstrated that treatment with a specific inhibitor of GSK3, SB216763, attenuated induction of mitochondrial biogenesis by a glycolysis inhibitor, 2-deoxyglucose (2-DG), without affecting this biogenesis at basal condition. Additionally, overexpression of WT-GSK3β promoted whereas GSK3β-KD attenuated 2-DG-induced mitochondrial protein expression. The mitochondrial biogenesis attenuation by GSK3 inhibitor was not due to inhibition of protein degradation. Furthermore, GSK3 inhibition further reduced transcription of mitochondrial (COXII), but not nuclear (VDAC) gene by 2-DG suggesting its participation in 2-DG-induced mitochondrial transcription. Together, our results show that GSK3 regulates mitochondrial biogenesis induced by glycolysis inhibition.
Keywords
GAPDHTK2GSK3PGC-1αNRF-1TFAMAMPKVDAC2-DeoxyglucoseMitochondrial cytochrome b2-DGAMP-activated protein kinaseThymidine kinase 2Mitochondrial biogenesisNuclear respiratory factor 1mitochondrial transcription factor Aperoxisome proliferator-activated receptor gamma coactivator 1αvoltage-dependent anion-selective channelglyceraldehyde-3-phosphate dehydrogenaseglycogen synthase kinase-3
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Authors
Pronrumpa Ngamsiri, Piyajit Watcharasit, Jutamaad Satayavivad,