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Author
- Bagshaw, Olivia1
- Braun, Jessica L1
- Cheng, Aoxing1
- Dhaliwal, Roopan1
- Duan, Xiaotao1
- Fajardo, Val A1
- Fan, Weiwei1
- Fenech, Rachel K1
- Finch, Michael S1
- Gardner, Georgina1
- Geromella, Mia S1
- Guo, Jing1
- Hamstra, Sophie I1
- Han, Chaoqiang1
- Hockey, Briana L1
- Jiang, Ya1
- Jin, Tengchuan1
- Liu, Xing1
- MacPherson, Rebecca EK1
- Maddalena, Lucas A1
- Marko, Daniel M1
- Moradi, Fereshteh1
- Roy, Brian D1
- Ruan, Ke1
- Ryan, Chantal R1
Metabolism
2 Results
- Research ArticleOpen Access
Low-dose lithium supplementation promotes adipose tissue browning and sarco(endo)plasmic reticulum Ca2+ ATPase uncoupling in muscle
Journal of Biological ChemistryVol. 298Issue 11102568Published online: October 6, 2022- Mia S. Geromella
- Chantal R. Ryan
- Jessica L. Braun
- Michael S. Finch
- Lucas A. Maddalena
- Olivia Bagshaw
- and others
Cited in Scopus: 1Sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) uncoupling in skeletal muscle and mitochondrial uncoupling via uncoupling protein 1 (UCP1) in brown/beige adipose tissue are two mechanisms implicated in energy expenditure. Here, we investigated the effects of glycogen synthase kinase 3 (GSK3) inhibition via lithium chloride (LiCl) treatment on SERCA uncoupling in skeletal muscle and UCP1 expression in adipose. C2C12 and 3T3-L1 cells treated with LiCl had increased SERCA uncoupling and UCP1 protein levels, respectively, ultimately raising cellular respiration; however, this was only observed when LiCl treatment occurred throughout differentiation. - Research ArticleOpen Access
Aurora A–mediated pyruvate kinase M2 phosphorylation promotes biosynthesis with glycolytic metabolites and tumor cell cycle progression
Journal of Biological ChemistryVol. 298Issue 11102561Published online: October 1, 2022- Ya Jiang
- Ting Wang
- Dandan Sheng
- Chaoqiang Han
- Tian Xu
- Peng Zhang
- and others
Cited in Scopus: 0Cancer cells have distinctive demands for intermediates from glucose metabolism for biosynthesis and energy in different cell cycle phases. However, how cell cycle regulators and glycolytic enzymes coordinate to orchestrate the essential metabolic processes are still poorly characterized. Here, we report a novel interaction between the mitotic kinase, Aurora A, and the glycolytic enzyme, pyruvate kinase M2 (PKM2), in the interphase of the cell cycle. We found Aurora A–mediated phosphorylation of PKM2 at threonine 45.