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The Role of Myocardial Mitochondrial Quality Control in Heart Failure

https://doi.org/10.3389/fphar.2019.01404

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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SIRT3 deficiency impairs mitochondrial and contractile function in the heart

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Effect of the stop-flow technique on cardiac retention of c-kit positive human cardiac stem cells after intracoronary infusion in a porcine model of chronic ischemic cardiomyopathy

inferredcites →https://doi.org/10.1007/s00441-016-2485-8openalex-snapshot

Mitochondrial quality control by the Pink1/Parkin system

inferredcites →https://doi.org/10.1007/s00441-016-2533-4openalex-snapshot

Recent advances in mitochondrial biology - integrated aspects

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Mitochondrial dynamics and cell death in heart failure

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Hypoxia and mitochondrial oxidative metabolism

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Non-histone lysine acetylated proteins in heart failure

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Recent advances into the understanding of mitochondrial fission

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Mitochondrial dynamics and viral infections: A close nexus

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IRF4 Is a Key Thermogenic Transcriptional Partner of PGC-1α

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Induction of heart failure by minimally invasive aortic constriction in mice: Reduced peroxisome proliferator-activated receptor γ coactivator levels and mitochondrial dysfunction

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Regulation of mitochondrial biogenesis and PGC-1α under cellular stress

inferredcites →https://doi.org/10.1016/j.mito.2013.04.002openalex-snapshot

Dual control of mitochondrial biogenesis by sirtuin 1 and sirtuin 3

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SIRT3 Deficiency and Mitochondrial Protein Hyperacetylation Accelerate the Development of the Metabolic Syndrome

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Parkinson's disease proteins: Novel mitochondrial targets for cardioprotection

inferredcites →https://doi.org/10.1016/j.redox.2017.11.004openalex-snapshot

DUSP1 alleviates cardiac ischemia/reperfusion injury by suppressing the Mff-required mitochondrial fission and Bnip3-related mitophagy via the JNK pathways

inferredcites →https://doi.org/10.1016/j.tem.2012.06.006openalex-snapshot

Transcriptional integration of mitochondrial biogenesis

inferredcites →https://doi.org/10.1016/j.yjmcc.2008.10.025openalex-snapshot

PGC-1α and ERRα target gene downregulation is a signature of the failing human heart

inferredcites →https://doi.org/10.1016/j.yjmcc.2011.01.008openalex-snapshot

Emerging roles of SIRT1 deacetylase in regulating cardiomyocyte survival and hypertrophy

inferredcites →https://doi.org/10.1016/j.yjmcc.2014.09.019openalex-snapshot

Molecular mechanisms mediating mitochondrial dynamics and mitophagy and their functional roles in the cardiovascular system

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Nuclear activators and coactivators in mammalian mitochondrial biogenesis

inferredcites →https://doi.org/10.1038/ncomms4550openalex-snapshot

Acidosis overrides oxygen deprivation to maintain mitochondrial function and cell survival

inferredcites →https://doi.org/10.1038/nrm3028openalex-snapshot

Mechanisms of mitophagy

inferredcites →https://doi.org/10.1038/nrm3293openalex-snapshot

Sirtuins as regulators of metabolism and healthspan

inferredcites →https://doi.org/10.1038/s41418-018-0086-7openalex-snapshot

Pathogenesis of cardiac ischemia reperfusion injury is associated with CK2α-disturbed mitochondrial homeostasis via suppression of FUNDC1-related mitophagy

inferredcites →https://doi.org/10.1038/sj.emboj.7601963openalex-snapshot

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

inferredcites →https://doi.org/10.1042/bse0470085openalex-snapshot

Mitochondrial fission and fusion

inferredcites →https://doi.org/10.1056/nejmra1215233openalex-snapshot

Mitochondrial Dynamics — Mitochondrial Fission and Fusion in Human Diseases

inferredcites →https://doi.org/10.1074/jbc.m109.090266openalex-snapshot

Induction of Manganese Superoxide Dismutase by Nuclear Translocation and Activation of SIRT1 Promotes Cell Survival in Chronic Heart Failure

inferredcites →https://doi.org/10.1074/jbc.m112.411363openalex-snapshot

Parkin Protein Deficiency Exacerbates Cardiac Injury and Reduces Survival following Myocardial Infarction

inferredcites →https://doi.org/10.1074/jbc.m206958200openalex-snapshot

Mitochondrial Transcription Factor A and Its Downstream Targets Are Up-regulated in a Rat Hepatoma

inferredcites →https://doi.org/10.1074/jbc.m406960200openalex-snapshot

Uth1p Is Involved in the Autophagic Degradation of Mitochondria

inferredcites →https://doi.org/10.1083/jcb.200704112openalex-snapshot

Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage

inferredcites →https://doi.org/10.1083/jcb.201007152openalex-snapshot

Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells

inferredcites →https://doi.org/10.1083/jcb.201507035openalex-snapshot

Titration of mitochondrial fusion rescues Mff -deficient cardiomyopathy

inferredcites →https://doi.org/10.1083/jcb.201611048openalex-snapshot

Mitochondrial fusion: Reaching the end of mitofusin’s tether

inferredcites →https://doi.org/10.1089/rej.2005.8.3openalex-snapshot

Selective Mitochondrial Autophagy, or Mitophagy, as a Targeted Defense Against Oxidative Stress, Mitochondrial Dysfunction, and Aging

inferredcites →https://doi.org/10.1091/mbc.e12-10-0721openalex-snapshot

Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission

inferredcites →https://doi.org/10.1093/cvr/cvp181openalex-snapshot

Mitochondrial OPA1, apoptosis, and heart failure

inferredcites →https://doi.org/10.1096/fj.14-253823openalex-snapshot

Maintaining PGC‐1α expression following pressure overload‐induced cardiac hypertrophy preserves angiogenesis but not contractile or mitochondrial function

inferredcites →https://doi.org/10.1097/hjh.0b013e3282f293c8openalex-snapshot

Forkhead class O transcription factor 3a activation and Sirtuin1 overexpression in the hypertrophied myocardium of the diabetic Goto-Kakizaki rat

inferredcites →https://doi.org/10.1111/bph.12516openalex-snapshot

Mitochondrial fusion and fission proteins: novel therapeutic targets for combating cardiovascular disease

inferredcites →https://doi.org/10.1111/febs.13820openalex-snapshot

Mitochondrial biogenesis and clearance: a balancing act

inferredcites →https://doi.org/10.1111/j.1749-6632.2012.06738.xopenalex-snapshot

Role of PGC‐1α signaling in skeletal muscle health and disease

inferredcites →https://doi.org/10.1124/pr.115.011502openalex-snapshot

Mitochondrial Quality Control as a Therapeutic Target

inferredcites →https://doi.org/10.1126/science.350.6264.1052-fopenalex-snapshot

Mitochondrial quality control

inferredcites →https://doi.org/10.1126/science.39.1000.330openalex-snapshot

Mitochondria in Tissue Culture

inferredcites →https://doi.org/10.1128/mcb.01636-07openalex-snapshot

Mammalian Sir2 Homolog SIRT3 Regulates Global Mitochondrial Lysine Acetylation

inferredcites →https://doi.org/10.1139/y08-099openalex-snapshot

Sirt1 hyperexpression in SHR heart related to left ventricular hypertrophy

inferredcites →https://doi.org/10.1152/ajpheart.00708.2014openalex-snapshot

Mending a broken heart: the role of mitophagy in cardioprotection

inferredcites →https://doi.org/10.1152/ajpheart.00734.2006openalex-snapshot

Restoration of CREB function is linked to completion and stabilization of adaptive cardiac hypertrophy in response to exercise

inferredcites →https://doi.org/10.1152/physrev.00025.2007openalex-snapshot

Transcriptional Paradigms in Mammalian Mitochondrial Biogenesis and Function

inferredcites →https://doi.org/10.1161/01.res.0000117088.36577.ebopenalex-snapshot

Cardiac-Specific Induction of the Transcriptional Coactivator Peroxisome Proliferator-Activated Receptor γ Coactivator-1α Promotes Mitochondrial Biogenesis and Reversible Cardiomyopathy in a Developmental Stage-Dependent Manner

inferredcites →https://doi.org/10.1161/01.res.0000147557.75257.ffopenalex-snapshot

Silent Information Regulator 2α, a Longevity Factor and Class III Histone Deacetylase, Is an Essential Endogenous Apoptosis Inhibitor in Cardiac Myocytes

inferredcites →https://doi.org/10.1161/01.res.0000267723.65696.4aopenalex-snapshot

Sirt1 Regulates Aging and Resistance to Oxidative Stress in the Heart

inferredcites →https://doi.org/10.1161/cir.0000000000000485openalex-snapshot

Heart Disease and Stroke Statistics—2017 Update: A Report From the American Heart Association

inferredcites →https://doi.org/10.1161/cir.0000000000000491openalex-snapshot

Correction to: Heart Disease and Stroke Statistics—2017 Update: A Report From the American Heart Association

inferredcites →https://doi.org/10.1161/circresaha.111.258723openalex-snapshot

Mitochondrial Fusion is Essential for Organelle Function and Cardiac Homeostasis

inferredcites →https://doi.org/10.1161/circresaha.117.312317openalex-snapshot

AMPKα2 Protects Against the Development of Heart Failure by Enhancing Mitophagy via PINK1 Phosphorylation

inferredcites →https://doi.org/10.1161/circresaha.118.312655openalex-snapshot

Regulating Renewable Energy

inferredcites →https://doi.org/10.1161/circulationaha.107.763870openalex-snapshot

Intracellular Protein Aggregation Is a Proximal Trigger of Cardiomyocyte Autophagy

inferredcites →https://doi.org/10.1161/circulationaha.110.958033openalex-snapshot

Silent Information Regulator 1 Protects the Heart From Ischemia/Reperfusion

inferredcites →https://doi.org/10.1161/hypertensionaha.111.174128openalex-snapshot

AMP Activated Protein Kinase-α2 Regulates Expression of Estrogen-Related Receptor-α, a Metabolic Transcription Factor Related to Heart Failure Development

inferredcites →https://doi.org/10.1161/jaha.116.005328openalex-snapshot

Mff‐Dependent Mitochondrial Fission Contributes to the Pathogenesis of Cardiac Microvasculature Ischemia/Reperfusion Injury via Induction of mROS‐Mediated Cardiolipin Oxidation and HK2/VDAC1 Disassociation‐Involved mPTP Opening

inferredcites →https://doi.org/10.1172/jci10268openalex-snapshot

Peroxisome proliferator–activated receptor γ coactivator-1 promotes cardiac mitochondrial biogenesis

inferredcites →https://doi.org/10.1172/jci39162openalex-snapshot

Sirt3 blocks the cardiac hypertrophic response by augmenting Foxo3a-dependent antioxidant defense mechanisms in mice

inferredcites →https://doi.org/10.1194/jlr.m060533openalex-snapshot

PGC-1α-mediated changes in phospholipid profiles of exercise-trained skeletal muscle

inferredcites →https://doi.org/10.1371/journal.pone.0011707openalex-snapshot

Sirtuin 3, a New Target of PGC-1α, Plays an Important Role in the Suppression of ROS and Mitochondrial Biogenesis

inferredcites →https://doi.org/10.1371/journal.pone.0032388openalex-snapshot

Mitochondrial division/mitophagy inhibitor (Mdivi) Ameliorates Pressure Overload Induced Heart Failure

inferredcites →https://doi.org/10.1536/ihj.48.533openalex-snapshot

Losartan Preserves Integrity of Cardiac Gap Junctions and PGC-1 .ALPHA. Gene Expression and Prevents Cellular Apoptosis in Remote Area of Left Ventricular Myocardium Following Acute Myocardial Infarction

inferredcites →https://doi.org/10.18632/aging.100075openalex-snapshot

Diet and exercise signals regulate SIRT3 and activate AMPK and PGC-1α in skeletal muscle

inferredcites →https://doi.org/10.2337/db14-0325openalex-snapshot

ATGL-Catalyzed Lipolysis Regulates SIRT1 to Control PGC-1α/PPAR-α Signaling

inferredcites →https://doi.org/10.4161/auto.3930openalex-snapshot

ER-Phagy: Selective Autophagy of the Endoplasmic Reticulum

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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DUSP1 interacts with and dephosphorylates VCP to improve mitochondrial quality control against endotoxemia-induced myocardial dysfunction

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Functional, structural, and molecular remodelling of the goldfish (Carassius auratus) heart under moderate hypoxia

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Mitochondrial Toxicity of PM2.5 Leads to Cardiac Failure: A Comparative Evaluation of PM2.5 from Ambient Air, Diesel Exhaust and SRM 2975

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Additional file 2 of A circular network of purine metabolism as coregulators of dilated cardiomyopathy

inferred← citeshttps://doi.org/10.6084/m9.figshare.21601682openalex-snapshot

Additional file 3 of A circular network of purine metabolism as coregulators of dilated cardiomyopathy

inferred← citeshttps://doi.org/10.6084/m9.figshare.21601685openalex-snapshot

Additional file 4 of A circular network of purine metabolism as coregulators of dilated cardiomyopathy

inferred← citeshttps://doi.org/10.6084/m9.figshare.21601688openalex-snapshot

Additional file 5 of A circular network of purine metabolism as coregulators of dilated cardiomyopathy

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703364openalex-snapshot

Additional file 1 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703367openalex-snapshot

Additional file 2 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703370openalex-snapshot

Additional file 3 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703376openalex-snapshot

Additional file 4 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703385openalex-snapshot

Additional file 5 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703388openalex-snapshot

Additional file 6 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703391openalex-snapshot

Additional file 7 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703394openalex-snapshot

Additional file 8 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703397openalex-snapshot

Additional file 9 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703400openalex-snapshot

Additional file 10 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703403openalex-snapshot

Additional file 11 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703406openalex-snapshot

Additional file 12 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703409openalex-snapshot

Additional file 13 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

inferred← citeshttps://doi.org/10.6084/m9.figshare.26703412openalex-snapshot

Additional file 14 of Pangenome and multi-tissue gene atlas provide new insights into the domestication and highland adaptation of yaks

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