Journal
REDOX BIOLOGY
Volume 45, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.redox.2021.102043
Keywords
Proteasome; Liver; ASK1; PPAR gamma; NASH
Categories
Funding
- Indian Council of Medical Research (ICMR), India [5/4/5-9/Diab.-16-NCD-II]
- Council of Scientific and IndustrialResearch (CSIR), India [MLP125, MLP138]
- University Grants Commission (UGC), India
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The incidence of hepatotoxicity in obesity and insulin resistance emphasizes the importance of liver protein homeostasis. The susceptibility of hepatocytes to proteasome-associated metabolic stress under altered redox homeostasis is crucial. Inhibition of ASK1 can rescue acute hepatotoxicity, but depletion of PPAR gamma may aggravate liver injury, highlighting the importance of endogenous PPAR gamma-driven antioxidant activity for favorable therapeutic outcomes.
Incidence of hepatotoxicity following acute drug-induced proteasomal inhibition and development of chronic proteasome dysfunction in obesity and insulin resistance underscores the crucial importance of hepatic protein homeostasis albeit with an elusive molecular basis and therapeutic opportunities. Apart from lipotoxicity and endoplasmic reticulum (ER) stress, herein we report that hepatocytes are highly susceptible to proteasomeassociated metabolic stress attune to altered redox homeostasis. Bortezomib-induced proteasomal inhibition caused severe hepatocellular injury independent of ER stress via proapoptotic Apoptosis Signal-regulating Kinase 1 (ASK1)-c-Jun N-terminal kinase (JNK1)- p38 signaling concomitant with inadequate peroxisome proliferatoractivated receptor gamma (PPAR gamma)- Nuclear factor erythroid 2-related factor 2 (Nrf2)-driven antioxidant response. Although inhibition of ASK1 rescued acute hepatotoxicity, hepatic depletion of PPAR gamma or its physiological activator pigment epithelium-derived factor (PEDF) further aggravated liver injury even under ASK1 inhibition, emphasizing that endogenous PPAR gamma driven antioxidant activity serves as a prerequisite for the favorable therapeutic outcome of ASK1 inhibition. Consequently, ASK1 inhibitor selonsertib and PPAR gamma agonist pioglitazone in pharmacological synergism ameliorated bortezomib-induced hepatotoxicity and significantly prolonged survival duration in mice. Moreover, we showed that proteasome dysfunction is associated with ASK1 activation and insufficient PPAR gamma/Nrf2-driven antioxidative response in a subset of human nonalcoholic steatohepatitis (NASH) patients and the preclinical NASH model. The latter remains highly responsive to the drug combination marked by revamped proteasomal activity and alleviated hallmarks of NASH such as steatosis, fibrosis, and hepatocellular death. We thus uncovered a pharmacologically amenable interdependent binodal molecular circuit underlying hepatic proteasomal dysfunction and associated oxidative injury.
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