Impaired Protein Quality Control During Left Ventricular Remodeling in Mice With Cardiac Restricted Overexpression of Tumor Necrosis Factor. (December 2017)

• Record Type: Journal Article
• Authors: Hartupee, Justin; Szalai, Gabor D.; Wang, Wei; Ma, Xiucui; Diwan, Abhinav; Mann, Douglas L.
• Is Part Of: Circulation. Volume 10:Number 12(2017)
• Publication Date: 2017-12
• Subjects: autophagy -- inflammation -- myocarditis -- tumor necrosis factor -- ubiquitin; Heart failure -- Periodicals; 616.129005
• DOI: 10.1161/CIRCHEARTFAILURE.117.004252
• Languages: English
• ISSNs: 1941-3289

Abstract

Abstract : Background: Sustained inflammation in the heart is sufficient to provoke left ventricular dysfunction and left ventricular remodeling. Although inflammation has been linked to many of the biological changes responsible for adverse left ventricular remodeling, the relationship between inflammation and protein quality control in the heart is not well understood. Methods and Results: To study the relationship between chronic inflammation and protein quality control, we used a mouse model of dilated cardiomyopathy driven by cardiac restricted overexpression of TNF (tumor necrosis factor; Myh6 -sTNF). Myh6 -sTNF mice develop protein aggregates containing ubiquitin-tagged proteins within cardiac myocytes related to proteasome dysfunction and impaired autophagy. The 26S proteasome was dysfunctional despite normal function of the core 20S subunit. We found an accumulation of autophagy substrates in Myh6 -sTNF mice, which were also seen in tissue from patients with end-stage heart failure. Moreover, there was evidence of impaired autophagosome clearance after chloroquine administration in these mice indicative of impaired autophagic flux. Finally, there was increased mammalian target of rapamycin complex 1 (mTORC1) activation, which has been linked to inhibition of both the proteasome and autophagy. Conclusions: Myh6 -sTNF mice with sustained inflammatory signaling develop proteasome dysfunction and impaired autophagic flux that is associated with enhanced mTORC1 activation. Abstract : Supplemental Digital Content is available in the text.