Myocardial glycophagy flux dysregulation and glycogen accumulation characterize diabetic cardiomyopathy

IF 4.9 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of molecular and cellular cardiology Pub Date : 2024-03-13 DOI:10.1016/j.yjmcc.2024.02.009
Kimberley M. Mellor , Upasna Varma , Parisa Koutsifeli , Lorna J. Daniels , Victoria L. Benson , Marco Annandale , Xun Li , Yohanes Nursalim , Johannes V. Janssens , Kate L. Weeks , Kim L. Powell , Terence J. O'Brien , Rajesh Katare , Rebecca H. Ritchie , James R. Bell , Roberta A. Gottlieb , Lea M.D. Delbridge
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Abstract

Diabetic heart disease morbidity and mortality is escalating. No specific therapeutics exist and mechanistic understanding of diabetic cardiomyopathy etiology is lacking. While lipid accumulation is a recognized cardiomyocyte phenotype of diabetes, less is known about glycolytic fuel handling and storage. Based on in vitro studies, we postulated the operation of an autophagy pathway in the myocardium specific for glycogen homeostasis – glycophagy. Here we visualize occurrence of cardiac glycophagy and show that the diabetic myocardium is characterized by marked glycogen elevation and altered cardiomyocyte glycogen localization. We establish that cardiac glycophagy flux is disturbed in diabetes. Glycophagy may represent a potential therapeutic target for alleviating the myocardial impacts of metabolic disruption in diabetic heart disease.

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心肌糖吞噬通量失调和糖原累积是糖尿病心肌病的特征
糖尿病心脏病的发病率和死亡率不断攀升。目前尚无特效疗法,也缺乏对糖尿病心肌病病因机制的了解。脂质积累是公认的糖尿病心肌细胞表型,但对糖酵解燃料的处理和储存却知之甚少。根据体外研究,我们推测心肌中存在一种专门用于糖原平衡的自噬途径--糖噬。在这里,我们对心肌糖吞噬的发生进行了可视化,并显示糖尿病心肌的特征是明显的糖原升高和心肌细胞糖原定位的改变。我们确定糖尿病患者的心肌糖吞噬通量受到干扰。糖吞噬可能是缓解糖尿病心脏病代谢紊乱对心肌影响的潜在治疗靶点。
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CiteScore
10.70
自引率
0.00%
发文量
171
审稿时长
42 days
期刊介绍: The Journal of Molecular and Cellular Cardiology publishes work advancing knowledge of the mechanisms responsible for both normal and diseased cardiovascular function. To this end papers are published in all relevant areas. These include (but are not limited to): structural biology; genetics; proteomics; morphology; stem cells; molecular biology; metabolism; biophysics; bioengineering; computational modeling and systems analysis; electrophysiology; pharmacology and physiology. Papers are encouraged with both basic and translational approaches. The journal is directed not only to basic scientists but also to clinical cardiologists who wish to follow the rapidly advancing frontiers of basic knowledge of the heart and circulation.
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Editorial Board PERM1 regulates mitochondrial energetics through O-GlcNAcylation in the heart Corrigendum to "PGE2 protects against heart failure through inhibiting TGF-β1 synthesis in cardiomyocytes and crosstalk between TGF-β1 and GRK2" [Journal of Molecular and Cellular Cardiology. 172(2022) 63-77]. Retraction notice to “The novel antibody fusion protein rhNRG1-HER3i promotes heart regeneration by enhancing NRG1-ERBB4 signaling pathway” [Journal of Molecular and Cellular Cardiology 187 (2023) 26–37] Exercise training attenuates cardiac dysfunction induced by excessive sympathetic activation through an AMPK-KLF4-FMO2 axis
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