BaCKgRoUND aND aIMS: Despite the high clinical significance of sarcopenia in alcohol-associated cirrhosis, there are currently no effective therapies because the underlying mechanisms are poorly understood. We determined the mechanisms of ethanol-induced impaired phosphorylation of mechanistic target of rapamycin complex 1 (mTORC1) and adenosine monophosphate-activated protein kinase (AMPK) with consequent dysregulated skeletal muscle protein homeostasis (balance between protein synthesis and breakdown). appRoaCH aND ReSUltS: Differentiated murine myotubes, gastrocnemius muscle from mice with loss and gain of function of regulatory genes following ethanol treatment, and skeletal muscle from patients with alcohol-associated cirrhosis were used. Ethanol increases skeletal muscle autophagy by dephosphorylating mTORC1, circumventing the classical kinase regulation by protein kinase B (Akt). Concurrently and paradoxically, ethanol exposure results in dephosphorylation and inhibition of AMPK, an activator of autophagy and inhibitor of mTORC1 signaling. However, AMPK remains inactive with ethanol exposure despite lower cellular and tissue adenosine triphosphate, indicating a "pseudofed" state. We identified protein phosphatase (PP) 2A as a key mediator of ethanol-induced signaling and functional perturbations using loss and gain of function studies. Ethanol impairs binding of endogenous inhibitor of PP2A to PP2A, resulting in methylation and targeting of PP2A to cause dephosphorylation of mTORC1 and AMPK. Activity of phosphoinositide 3-kinaseγ (PI3Kγ), a negative regulator of PP2A, was decreased in response to ethanol. Ethanol-induced molecular and phenotypic perturbations in wild-type mice were observed in PI3Kγ −/− mice even at baseline. Importantly, overexpressing kinase-active PI3Kγ but not the kinase-dead mutant reversed ethanol-induced molecular perturbations.
CoNClUSIoNS:Our study describes the mechanistic underpinnings for ethanol-mediated dysregulation of protein homeostasis by PP2A that leads to sarcopenia with a potential for therapeutic approaches by targeting the PI3Kγ-PP2A axis.
Figure 1. Multivariable logistic regression analysis of possible predictors for major depressive disorder (MDD) in patients with ulcerative colitis. Subgroup analysis stratified by gender. Forrest plot showing adjusted odds (OR); 95% confidence interval.Table 1. Baseline characteristics of patients with ulcerative colitis included in the study Characteristics MDD Diagnosis (N51,495) Absence of MDD Diagnosis (N5204,045) Total (N) Prevalence (%) 95% CI Total (N) Prevalence (%) 95% CI Tofacitinib use Yes 25 0.62
Figure 1. Forest plots summarizing the pooled frequency of (A) ischemic hepatitis, (B) viral hepatitis, (C) drug or toxin injury, and (D) extrahepatic biliary obstruction among patients presenting with extreme transaminase elevation.
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