Browsing by Author "Baker, Talia B."

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    Cardiolipin deficiency disrupts CoQ redox state and induces steatohepatitis
    (bioRxiv, 2024-10-10) Brothwell, Marisa J.; Cao, Guoshen; Maschek, J. Alan; Poss, Annelise M.; Peterlin, Alek D.; Wang, Liping; Baker, Talia B.; Shahtout, Justin L.; Siripoksup, Piyarat; Pearce, Quentinn J.; Johnson, Jordan M.; Finger, Fabian M.; Prola, Alexandre; Pellizzari, Sarah A.; Hale, Gillian L.; Manuel, Allison M.; Watanabe, Shinya; Miranda, Edwin R.; Affolter, Kajsa E.; Tippetts, Trevor S.; Nikolova, Linda S.; Choi, Ran Hee; Decker, Stephen T.; Patil, Mallikarjun; Catrow, J. Leon; Holland, William L.; Nowinski, Sara M.; Lark, Daniel S.; Fisher-Wellman, Kelsey H.; Mimche, Patrice N.; Evason, Kimberley J.; Cox, James E.; Summers, Scott A.; Gerhart-Hines, Zach; Funai, Katsuhiko; Dermatology, School of Medicine
    Metabolic dysfunction-associated steatotic liver disease (MASLD) is a progressive disorder marked by lipid accumulation, leading to steatohepatitis (MASH). A key feature of the transition to MASH involves oxidative stress resulting from defects in mitochondrial oxidative phosphorylation (OXPHOS). Here, we show that pathological alterations in the lipid composition of the inner mitochondrial membrane (IMM) directly instigate electron transfer inefficiency to promote oxidative stress. Specifically, cardiolipin (CL) was downregulated across four mouse models of MASLD. Hepatocyte-specific CL synthase knockout (CLS-LKO) led to spontaneous MASH with elevated mitochondrial electron leak. Loss of CL interfered with the ability of coenzyme Q (CoQ) to transfer electrons, promoting leak primarily at sites IIF and IIIQ0. Data from human liver biopsies revealed a highly robust correlation between mitochondrial CL and CoQ, co-downregulated with MASH. Thus, reduction in mitochondrial CL promotes oxidative stress and contributes to pathogenesis of MASH.