Inhibition of mitoNEET attenuates LPS-induced inflammation and oxidative stress
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[1] Santosh Shenoy. Coronavirus (Covid-19) sepsis: revisiting mitochondrial dysfunction in pathogenesis, aging, inflammation, and mortality , 2020, Inflammation Research.
[2] H. Ding,et al. Exploring the FMN binding site in the mitochondrial outer membrane protein mitoNEET. , 2020, Free radical biology & medicine.
[3] R. Bronson,et al. Expression of Stromal Cell–Derived Factor-1 by Mesenchymal Stromal Cells Impacts Neutrophil Function During Sepsis , 2020, Critical care medicine.
[4] Y. Belay,et al. Mitochondrial Dynamic Dysfunction as a Main Triggering Factor for Inflammation Associated Chronic Non-Communicable Diseases , 2020, Journal of inflammation research.
[5] R. Lill,et al. Glycogen branching enzyme controls cellular iron homeostasis via Iron Regulatory Protein 1 and mitoNEET , 2019, Nature Communications.
[6] H. Puthalakath,et al. Sepsis: Inflammation Is a Necessary Evil , 2019, Front. Cell Dev. Biol..
[7] W. Geldenhuys,et al. The MitoNEET Ligand NL-1 Mediates Antileukemic Activity in Drug-Resistant B-Cell Acute Lymphoblastic Leukemia , 2019, The Journal of Pharmacology and Experimental Therapeutics.
[8] D. Richardson,et al. The Role of the Antioxidant Response in Mitochondrial Dysfunction in Degenerative Diseases: Cross-Talk between Antioxidant Defense, Autophagy, and Apoptosis , 2019, Oxidative medicine and cellular longevity.
[9] C. Pourzand,et al. The role of mitochondrial labile iron in Friedreich's ataxia skin fibroblasts sensitivity to ultraviolet A† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8mt00257f , 2019, Metallomics : integrated biometal science.
[10] Defang Li,et al. Isoliquiritigenin Induces Mitochondrial Dysfunction and Apoptosis by Inhibiting mitoNEET in a Reactive Oxygen Species-Dependent Manner in A375 Human Melanoma Cells , 2019, Oxidative medicine and cellular longevity.
[11] Yong-ming Yao,et al. Potential therapy strategy: targeting mitochondrial dysfunction in sepsis , 2018, Military Medical Research.
[12] M. Reale,et al. Immune and Inflammatory-Mediated Disorders: From Bench to Bedside , 2018, Journal of immunology research.
[13] J. Vincent,et al. Mechanisms and treatment of organ failure in sepsis , 2018, Nature Reviews Nephrology.
[14] J. Lyu,et al. Electron transfer kinetics of the mitochondrial outer membrane protein mitoNEET , 2018, Free radical biology & medicine.
[15] Cuk-Seong Kim,et al. Role of Mitochondrial Oxidative Stress in Sepsis , 2018, Acute and critical care.
[16] Chung,et al. NOD2 deficiency exacerbates hypoxia-induced pulmonary hypertension and enhances pulmonary vascular smooth muscle cell proliferation , 2018, Oncotarget.
[17] K. Nakayama,et al. mitoNEET Regulates Mitochondrial Iron Homeostasis Interacting with Transferrin Receptor , 2017, bioRxiv.
[18] S. Ryter,et al. NLRP3 Inflammasome Deficiency Protects against Microbial Sepsis via Increased Lipoxin B4 Synthesis , 2017, American journal of respiratory and critical care medicine.
[19] E. Zakynthinos,et al. Role of Oxidative Stress and Mitochondrial Dysfunction in Sepsis and Potential Therapies , 2017, Oxidative medicine and cellular longevity.
[20] A. Bagchi,et al. Iron Loading Exaggerates the Inflammatory Response to the Toll-like Receptor 4 Ligand Lipopolysaccharide by Altering Mitochondrial Homeostasis , 2017, Anesthesiology.
[21] H. Ding,et al. The mitochondrial outer membrane protein mitoNEET is a redox enzyme catalyzing electron transfer from FMNH2 to oxygen or ubiquinone , 2017, The Journal of Biological Chemistry.
[22] W. Geldenhuys,et al. Identification of small molecules that bind to the mitochondrial protein mitoNEET. , 2016, Bioorganic & medicinal chemistry letters.
[23] H. Yao,et al. Mitochondrial dysfunction in inflammatory responses and cellular senescence: pathogenesis and pharmacological targets for chronic lung diseases , 2016, British journal of pharmacology.
[24] R. Lichtinghagen,et al. MitoNEET Protects HL-1 Cardiomyocytes from Oxidative Stress Mediated Apoptosis in an In Vitro Model of Hypoxia and Reoxygenation , 2016, PloS one.
[25] C. O’Farrelly,et al. Liver immunology and its role in inflammation and homeostasis , 2016, Cellular & Molecular Immunology.
[26] Hye-Ja Lee,et al. Effect of excess iron on oxidative stress and gluconeogenesis through hepcidin during mitochondrial dysfunction. , 2015, The Journal of nutritional biochemistry.
[27] W. Geldenhuys,et al. Novel thiazolidinedione mitoNEET ligand-1 acutely improves cardiac stem cell survival under oxidative stress , 2015, Basic Research in Cardiology.
[28] Shulin Li,et al. The Role of the Liver in Sepsis , 2014, International reviews of immunology.
[29] W. Geldenhuys,et al. mitoNEET as a novel drug target for mitochondrial dysfunction. , 2014, Drug discovery today.
[30] P. Scherer,et al. MitoNEET-Mediated Effects on Browning of White Adipose Tissue , 2014, Nature Communications.
[31] M. Núñez,et al. The interplay between iron accumulation, mitochondrial dysfunction, and inflammation during the execution step of neurodegenerative disorders , 2014, Front. Pharmacol..
[32] J. Onuchic,et al. NAF-1 and mitoNEET are central to human breast cancer proliferation by maintaining mitochondrial homeostasis and promoting tumor growth , 2013, Proceedings of the National Academy of Sciences.
[33] M. J. López-Armada,et al. Mitochondrial dysfunction and the inflammatory response. , 2013, Mitochondrion.
[34] D. McClain,et al. MitoNEET-driven alterations in adipocyte mitochondrial activity reveal a crucial adaptive process that preserves insulin sensitivity in obesity , 2012, Nature Medicine.
[35] P. Jennings,et al. NADPH Inhibits [2Fe-2S] Cluster Protein Transfer from Diabetes Drug Target MitoNEET to an Apo-acceptor Protein* , 2012, The Journal of Biological Chemistry.
[36] L. Boscá,et al. Anti-inflammatory and antioxidant properties of a new arylidene-thiazolidinedione in macrophages. , 2011, Current medicinal chemistry.
[37] J. Onuchic,et al. Facile transfer of [2Fe-2S] clusters from the diabetes drug target mitoNEET to an apo-acceptor protein , 2011, Proceedings of the National Academy of Sciences.
[38] W. Geldenhuys,et al. Structure-based design of a thiazolidinedione which targets the mitochondrial protein mitoNEET. , 2010, Bioorganic & medicinal chemistry letters.
[39] S. Levi,et al. The role of iron in mitochondrial function. , 2009, Biochimica et biophysica acta.
[40] Michael P. Murphy,et al. How mitochondria produce reactive oxygen species , 2008, The Biochemical journal.
[41] G. Bing,et al. Protective properties afforded by pioglitazone against intrastriatal LPS in Sprague–Dawley rats , 2008, Neuroscience Letters.
[42] T. Santa-Coloma,et al. CISD1 codifies a mitochondrial protein upregulated by the CFTR channel. , 2008, Biochemical and biophysical research communications.
[43] J. Dixon,et al. MitoNEET is a uniquely folded 2Fe–2S outer mitochondrial membrane protein stabilized by pioglitazone , 2007, Proceedings of the National Academy of Sciences.
[44] J. Dixon,et al. The Outer Mitochondrial Membrane Protein mitoNEET Contains a Novel Redox-active 2Fe-2S Cluster* , 2007, Journal of Biological Chemistry.
[45] J. Dixon,et al. MitoNEET is an iron-containing outer mitochondrial membrane protein that regulates oxidative capacity , 2007, Proceedings of the National Academy of Sciences.
[46] G. Hotamisligil,et al. Inflammation and metabolic disorders , 2006, Nature.
[47] Jingxiao Zhang,et al. Sepsis and immune response. , 2011, World journal of emergency medicine.