Low-dose lithium supplementation promotes adipose tissue browning and sarco(endo)plasmic reticulum Ca2+ ATPase uncoupling in muscle

• Published in: The Journal of biological chemistry Vol. 298; no. 11; p. 102568
• Main Authors: Geromella, Mia S., Ryan, Chantal R., Braun, Jessica L., Finch, Michael S., Maddalena, Lucas A., Bagshaw, Olivia, Hockey, Briana L., Moradi, Fereshteh, Fenech, Rachel K., Ryoo, Jisook, Marko, Daniel M., Dhaliwal, Roopan, Sweezey-Munroe, Jake, Hamstra, Sophie I., Gardner, Georgina, Silvera, Sebastian, Vandenboom, Rene, Roy, Brian D., Stuart, Jeffrey A., MacPherson, Rebecca E.K., Fajardo, Val A.
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01-11-2022; American Society for Biochemistry and Molecular Biology
• Subjects: beige; efficiency; neuronatin; sarcolipin; SERCA; UCP1; uncoupling; sarcolipin; efficiency; LiCl; GTT; HFD; UCP1; ITT; PGC-1α; RYR; SERCA; neuronatin; beige; iWAT; DMEM; uncoupling; SLN; BAT; GSK3; HSA; NNAT; KD; SR
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2022.102568

Sarco(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. In vivo, LiCl treatment (10 mg/kg/day) increased food intake in chow-fed diet and high-fat diet (HFD; 60% kcal)–fed male mice without increasing body mass—a result attributed to elevated daily energy expenditure. In soleus muscle, we determined that LiCl treatment promoted SERCA uncoupling via increased expression of SERCA uncouplers, sarcolipin and/or neuronatin, under chow-fed and HFD-fed conditions. We attribute these effects to the GSK3 inhibition observed with LiCl treatment as partial muscle-specific GSK3 knockdown produced similar effects. In adipose, LiCl treatment inhibited GSK3 in inguinal white adipose tissue (iWAT) but not in brown adipose tissue under chow-fed conditions, which led to an increase in UCP1 in iWAT and a beiging-like effect with a multilocular phenotype. We did not observe this beiging-like effect and increase in UCP1 in mice fed a HFD, as LiCl could not overcome the ensuing overactivation of GSK3. Nonetheless, our study establishes novel regulatory links between GSK3 and SERCA uncoupling in muscle and GSK3 and UCP1 and beiging in iWAT.