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1. Full Text Mitochondrial uncoupling protein 2 structure determined by NMR molecular fragment searching
by Berardi, Marcelo J and Shih, William M and Harrison, Stephen C and Chou, James J
Nature, ISSN 0028-0836, 08/2011, Volume 476, Issue 7358, pp. 109 - 114
Mitochondrial uncoupling protein 2 (UCP2) is an integral membrane protein in the mitochondrial anion carrier protein family, the members of which facilitate... 
INDUCED ALIGNMENT | SPECTROSCOPY | MECHANISM | MEMBRANE | MULTIDISCIPLINARY SCIENCES | NUCLEAR-MAGNETIC-RESONANCE | LIQUID-CRYSTALLINE PHASE | DIPOLAR COUPLINGS | ADP/ATP CARRIER | SECRETION | PROTON CHANNEL | Nitrogen Oxides - chemistry | Models, Molecular | Adenine Nucleotide Translocator 1 - metabolism | Animals | Mitochondrial ADP, ATP Translocases - chemistry | Adenine Nucleotide Translocator 1 - chemistry | Ion Channels - metabolism | Cattle | Mitochondrial Proteins - metabolism | Nuclear Magnetic Resonance, Biomolecular - methods | Databases, Protein | Mitochondrial Proteins - chemistry | Protein Conformation | Mice | Uncoupling Protein 2 | Guanosine Diphosphate - chemistry | Guanosine Diphosphate - metabolism | Nitrogen Oxides - metabolism | Binding Sites | Ion Channels - chemistry | Proteins | Lipids | Spectrum analysis | Methods | Deoxyribonucleic acid--DNA
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2. Full Text Uncoupling protein 2 and metabolic diseases
by Sreedhar, Annapoorna and Zhao, Yunfeng
Mitochondrion, ISSN 1567-7249, 05/2017, Volume 34, pp. 135 - 140
Mitochondria are fascinating organelles involved in various cellular-metabolic activities that are integral for mammalian development. Although they perform... 
Uncoupling proteins | Obesity | Metabolic disorder | Mitochondrial dysfunction | Diabetes | Cancer | OXYGEN SPECIES GENERATION | INSULIN-SECRETION | TISSUE-SPECIFIC EXPRESSION | BROWN ADIPOSE-TISSUE | NEURODEGENERATIVE DISEASES | CELL BIOLOGY | MESSENGER-RNA | FATTY-ACID OXIDATION | GENETICS & HEREDITY | CARDIOVASCULAR-DISEASE | BETA-CELL DYSFUNCTION | Animals | Metabolic Diseases - physiopathology | Energy Metabolism | Uncoupling Protein 2 - metabolism | Humans | Uncoupling Protein 2 - deficiency | Proteins | Physiological aspects | Neurosciences | mitochondrial dysfunction | cancer | diabetes | obesity | metabolic disorder
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3. Full Text Mitochondrial uncoupling protein 2 (UCP2) in glucose and lipid metabolism
by Diano, Sabrina and Horvath, Tamas L
Trends in Molecular Medicine, ISSN 1471-4914, 2011, Volume 18, Issue 1, pp. 52 - 58
Nutrient availability is critical for the physiological functions of all tissues. By contrast, an excess of nutrients such as carbohydrate and fats impair... 
Pathology | MEDICINE, RESEARCH & EXPERIMENTAL | HOMEOSTASIS | FOOD-INTAKE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ARCUATE NUCLEUS | BETA-CELL FUNCTION | FREE-RADICALS | CELL BIOLOGY | ENERGY-BALANCE | OBESITY | REACTIVE OXYGEN | FATTY-ACID OXIDATION | NEURONS | Reactive Oxygen Species - metabolism | Signal Transduction | Humans | Mitochondria - metabolism | Agouti-Related Protein - metabolism | Obesity - metabolism | Pro-Opiomelanocortin - metabolism | Insulin-Secreting Cells - metabolism | Animals | Hypothalamus - metabolism | Ion Channels - metabolism | Mitochondrial Proteins - metabolism | Glucagon-Secreting Cells - metabolism | Glucose - metabolism | Neurons - metabolism | Uncoupling Protein 2 | Lipid Metabolism - physiology | Glucose metabolism | Physiological aspects | Chronic diseases | Mitochondrial DNA | Glucose | Diabetes | Dextrose
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4. Full Text Superoxide activates mitochondrial uncoupling protein 2 from the matrix side: Studies using targeted antioxidants
by Echtay, Karim S and Murphy, Michael P and Smith, Robin A. J and Talbot, Darren A and Brand, Martin D
Journal of Biological Chemistry, ISSN 0021-9258, 12/2002, Volume 277, Issue 49, pp. 47129 - 47135
Superoxide activates nucleotide-sensitive mitochondrial proton transport through the uncoupling proteins UCP1, UCP2, and UCP3 (Echtay, K. S., et al. (2002)... 
YEAST | SKELETAL-MUSCLE | TRANSPORT | OBESITY | PROTON LEAK | UCP3 | BIOCHEMISTRY & MOLECULAR BIOLOGY | FATTY-ACIDS | MICE | COENZYME-Q | ADIPOSE-TISSUE | Aconitate Hydratase - metabolism | Protons | Reactive Oxygen Species | Ion Channels | Models, Chemical | Rats, Wistar | Ubiquinone - metabolism | Mitochondrial Proteins | Kidney - metabolism | Chromans - pharmacology | Time Factors | Superoxides - metabolism | Female | Cell Membrane - metabolism | Rats | Mitochondria - metabolism | Antioxidants - pharmacology | Mice, Knockout | Cyanides - metabolism | Animals | Proteins - metabolism | Membrane Potentials | Membrane Transport Proteins | Protein Binding | Cations | Mice | Uncoupling Protein 2 | Kinetics | Vitamin E - pharmacology
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5. Full Text Endothelial uncoupling protein 2 regulates mitophagy and pulmonary hypertension during intermittent hypoxia
by Haslip, Maria and Dostanic, Iva and Huang, Yan and Zhang, Yi and Russell, Kerry S and Jurczak, Michael J and Mannam, Praveen and Giordano, Frank and Erzurum, Serpil C and Lee, Patty J
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 05/2015, Volume 35, Issue 5, pp. 1166 - 1178
Objectives-Pulmonary hypertension (PH) is a process of lung vascular remodeling, which can lead to right heart dysfunction and significant morbidity. The... 
hypertension, pulmonary | endothelium | mitochondrial uncoupling protein 2 | autophagy | PTEN-induced putative kinase | mitochondrial degradation | APOPTOSIS | LUNG | MITOCHONDRIAL BIOGENESIS | CELL PROLIFERATION | MECHANISMS | MOUSE MODELS | DEFICIENCY | ARTERIAL | PERIPHERAL VASCULAR DISEASE | STRESS | HEMATOLOGY
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6. Full Text Uncoupling protein 2 reprograms the tumor microenvironment to support the anti-tumor immune cycle
by Cheng, Wan-Chen and Tsui, Yao-Chen and Ragusa, Simone and Koelzer, Viktor H and Mina, Marco and Franco, Fabien and Läubli, Heinz and Tschumi, Benjamin and Speiser, Daniel and Romero, Pedro and Zippelius, Alfred and Petrova, Tatiana V and Mertz, Kirsten and Ciriello, Giovanni and Ho, Ping-Chih
Nature Immunology, ISSN 1529-2908, 02/2019, Volume 20, Issue 2, pp. 206 - 217
Immune checkpoint blockade therapy has shifted the paradigm for cancer treatment. However, the majority of patients lack effective responses due to... 
MELANOMA | DENDRITIC CELLS | GENE | UCP2 | PROLIFERATION | CHECKPOINT | IRF5 | IMMUNOLOGY | NIVOLUMAB | BLOCKADE | EXPRESSION | Immunogenetics | Genetic aspects | Prognosis | Research | Tumors | Membrane proteins | Mitochondrial uncoupling protein 2 | Immunostimulation | Tumor cells | CD8 antigen | Lymphocytes T | Pharmacology | Anticancer properties | Metastases | Proteins | Mitochondria | Immune checkpoint | Cell death | Lymphocytes | Infiltration | Interferon | Interferon regulatory factor | Apoptosis | Cancer
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7. Full Text Uncoupling Protein 2 and Islet Function
by Catherine B. Chan and Monique C. Saleh and Vasilij Koshkin and Michael B. Wheeler
Diabetes, ISSN 0012-1797, 02/2004, Volume 53, Issue suppl 1, pp. S136 - S142
Stressors such as chronic hyperglycemia or hyperlipidemia may lead to insufficient insulin secretion in susceptible individuals, contributing to type 2... 
MITOCHONDRIAL SUPEROXIDE-PRODUCTION | CHRONIC EXPOSURE | STIMULATED INSULIN-SECRETION | MESSENGER-RNA | GENE | FATTY-ACID OXIDATION | PROTON LEAK | GLUCOSE | ENDOCRINOLOGY & METABOLISM | PANCREATIC BETA-CELL | EXPRESSION | Islets of Langerhans - physiology | Reactive Oxygen Species - metabolism | Ion Channels | Diabetes Mellitus, Type 2 - genetics | Humans | Gene Expression Regulation - physiology | Mitochondrial Proteins - physiology | Nutritional Physiological Phenomena | Membrane Transport Proteins - physiology | Insulin - metabolism | Animals | Diabetes Mellitus, Type 2 - physiopathology | Uncoupling Protein 2 | Insulin - genetics | Insulin Secretion
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8. Full Text UCP2-induced fatty acid synthase promotes NLRP3 inflammasome activation during sepsis
by Moon, Jong-Seok and Lee, Seonmin and Park, Mi-Ae and Siempos, Ilias I and Haslip, Maria and Lee, Patty J and Yun, Mijin and Kim, Chun K and Howrylak, Judie and Ryter, Stefan W and Nakahira, Kiichi and Choi, Augustine M. K
Journal of Clinical Investigation, ISSN 0021-9738, 02/2015, Volume 125, Issue 2, pp. 665 - 680
Cellular lipid metabolism has been linked to immune responses; however, the precise mechanisms by which de novo fatty acid synthesis can regulate inflammatory... 
MEDICINE, RESEARCH & EXPERIMENTAL | OXIDATIVE STRESS | GLUCOSE-METABOLISM | ATP-CITRATE LYASE | UCP2 | SEPTIC SHOCK | CELL-GROWTH | CRITICALLY-ILL PATIENTS | INTENSIVE INSULIN THERAPY | CANCER | MITOCHONDRIAL UNCOUPLING PROTEINS | Fatty Acid Synthase, Type I - genetics | Fatty Acid Synthase, Type I - biosynthesis | Lipids - genetics | Inflammasomes - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein | Humans | Ion Channels - genetics | Caspase 1 - metabolism | Mitochondrial Proteins - genetics | Interleukin-1beta - genetics | Lipids - biosynthesis | Sepsis - pathology | Interleukin-1beta - metabolism | Mitochondrial Proteins - metabolism | Sepsis - metabolism | Macrophages - pathology | Down-Regulation - genetics | Inflammasomes - genetics | Sepsis - genetics | Mice, Knockout | Carrier Proteins - genetics | Enzyme Induction - genetics | Macrophages - metabolism | Animals | Carrier Proteins - metabolism | Sepsis - chemically induced | Ion Channels - metabolism | Caspase 1 - genetics | Sepsis - therapy | Mice | Uncoupling Protein 2 | Interleukin-18 - genetics | Interleukin-18 - metabolism | Cellular proteins | Immune response | Synthesis | Sepsis | Development and progression | Lipids | Genetic aspects | Properties | Enzymes | Cytokines | Pathogenesis | Mortality | Glucose | Metabolism | Gene expression | Fatty acids | Proteins | Studies | Metabolites | Consent | Rodents
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9. Full Text Uncoupling protein 2 deficiency aggravates astrocytic endoplasmic reticulum stress and nod-like receptor protein 3 inflammasome activation
by Lu, Ming and Sun, Xiu-Lan and Qiao, Chen and Liu, Yang and Ding, Jian-Hua and Hu, Gang
Neurobiology of Aging, ISSN 0197-4580, 2014, Volume 35, Issue 2, pp. 421 - 430
Abstract Astrocytes play crucial roles in determining the susceptibility to oxidative stress in the brain, and uncoupling protein 2 (UCP2) has been... 
Neurology | Internal Medicine | Neuroinflammation | Parkinson's disease | Astrocyte | Uncoupling protein 2 | Endoplasmic reticulum stress | NLRP3 INFLAMMASOME | NEUROSCIENCES | DEGENERATION | GERIATRICS & GERONTOLOGY | PATHOGENESIS | MITOCHONDRIAL DYNAMICS | CELL-DEATH PROGRAM | MOUSE MODEL | UCP2 | DYSFUNCTION | NF-KAPPA-B | PARKINSONS-DISEASE | L-Lactate Dehydrogenase - metabolism | Parkinsonian Disorders | Tumor Necrosis Factor-alpha - metabolism | Tyrosine 3-Monooxygenase - metabolism | Reactive Oxygen Species - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein | Endoplasmic Reticulum - metabolism | Homeostasis | Glial Fibrillary Acidic Protein - metabolism | Interleukin-1beta - metabolism | Mitochondrial Proteins - deficiency | Disease Models, Animal | Astrocytes - cytology | Carrier Proteins - physiology | Oxidation-Reduction | Mice, Inbred C57BL | Cells, Cultured | Mitochondria - metabolism | Parkinson Disease - genetics | Inflammasomes - genetics | Mice, Knockout | Inflammasomes - physiology | Astrocytes - physiology | Animals | Endoplasmic Reticulum Stress | Mice | Uncoupling Protein 2 | Ion Channels - deficiency | Astrocytes - metabolism | Parkinson Disease - etiology
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10. Full Text The warburg effect in leukemia-stroma cocultures is mediated by mitochondrial uncoupling associated with uncoupling protein 2 activation
by Samudio, Ismael and Fiegl, Michael and McQueen, Teresa and Clise-Dwyer, Karen and Andreeff, Michael
Cancer Research, ISSN 0008-5472, 07/2008, Volume 68, Issue 13, pp. 5198 - 5205
In 1956, Otto Warburg proposed that the origin of cancer cells was closely linked to a permanent respiratory defect that bypassed the Pasteur effect (i.e., the... 
LEPTIN | THERMOGENESIS | APOPTOSIS | ONCOLOGY | FATTY-ACID OXIDATION | UCP2 | MYELOID-LEUKEMIA | TUMOR-CELLS | BROWN ADIPOSE-TISSUE | EXPRESSION | DINITROPHENOL | Uncoupling Agents - pharmacology | Coculture Techniques | Humans | Culture Media, Conditioned - pharmacology | Ion Channels - physiology | Leukemia - metabolism | Uncoupling Agents - metabolism | Membrane Potential, Mitochondrial - drug effects | Glycolysis - drug effects | Mitochondrial Proteins - metabolism | Stromal Cells - drug effects | Bone Marrow Cells - drug effects | Mesenchymal Stromal Cells - drug effects | Stromal Cells - metabolism | Cells, Cultured | Mesenchymal Stromal Cells - metabolism | Mitochondrial Proteins - physiology | Mitochondria - metabolism | Mitochondria - drug effects | Ion Channels - metabolism | HL-60 Cells | Uncoupling Protein 2 | Aerobiosis - physiology | Bone Marrow Cells - metabolism | Culture Media, Conditioned - metabolism | leukemia | uncoupling proteins | mitochondria | mesenchymal stromal cells | Warburg effect
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11. Full Text Resveratrol pretreatment protects rat brain from cerebral ischemic damage via a sirtuin 1–uncoupling protein 2 pathway
by Della-Morte, D and Dave, K.R and DeFazio, R.A and Bao, Y.C and Raval, A.P and Perez-Pinzon, M.A
Neuroscience, ISSN 0306-4522, 2009, Volume 159, Issue 3, pp. 993 - 1002
Abstract Resveratrol is a natural polyphenol found in grapes and wine and has been associated with protective effects against cardiovascular diseases. In vitro... 
Neurology | bioenergetics | cardiac arrest | cerebral ischemia | mitochondria | neuroprotection | tolerance | INSULIN-SECRETION | REPERFUSION | KINASE-C | MECHANISMS | NEUROSCIENCES | UCP2 | PANCREATIC BETA-CELLS | MICE | UNCOUPLING PROTEIN-2 | Carotid Artery Diseases - prevention & control | Stilbenes - administration & dosage | Hippocampus - drug effects | Stilbenes - pharmacology | Adenosine Triphosphate - biosynthesis | Membrane Potential, Mitochondrial - drug effects | Neuroprotective Agents - pharmacology | Mitochondrial Proteins - metabolism | Sirtuin 1 | Respiration - drug effects | Hypotension - prevention & control | Benzamides - pharmacology | Pyramidal Cells - drug effects | Neuroprotective Agents - administration & dosage | Disease Models, Animal | Pyramidal Cells - physiopathology | Signal Transduction | Naphthols - pharmacology | Rats | Brain Ischemia - prevention & control | Asphyxia | Heart Arrest | Rats, Sprague-Dawley | Animals | Ion Channels - metabolism | Uncoupling Protein 2 | Mitochondria - physiology | Sirtuins - antagonists & inhibitors | Hippocampus - physiopathology | Sirtuins - metabolism | Brain | Niacinamide | Coenzymes | Neurosciences | Dimethyl sulfoxide | Resveratrol | Adenine | Brain damage | Mitochondrial DNA
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12. Full Text Uncoupling Protein 2 Inhibition Exacerbates Glucose Fluctuation-Mediated Neuronal Effects
by Cardoso, Susana and Seiça, Raquel M and Moreira, Paula I
Neurotoxicity Research, ISSN 1029-8428, 2/2018, Volume 33, Issue 2, pp. 388 - 401
Though glucose fluctuations have been considered as an adverse factor for the development of several diabetes-related complications, their impact in the... 
Neurochemistry | Neurology | Neurosciences | Mitochondria | Neuronal cells | Biomedicine | Uncoupling protein 2 | Neurobiology | Pharmacology/Toxicology | Cell Biology | Genipin | Glucose variations | ENHANCES APOPTOSIS | OXIDATIVE STRESS | MITOCHONDRIAL BIOGENESIS | INFLAMMASOME ACTIVATION | PROTON-LEAK | VEIN ENDOTHELIAL-CELLS | NEUROSCIENCES | DIABETES-MELLITUS | BRAIN MITOCHONDRIA | IN-VITRO | GLYCEMIC VARIABILITY | Cell Survival - drug effects | Reactive Oxygen Species - metabolism | Rats, Wistar | Uncoupling Protein 2 - metabolism | Mitochondria - metabolism | Mitochondria - drug effects | Membrane Potential, Mitochondrial - drug effects | Pyrethrins - pharmacology | Animals | Uncoupling Protein 2 - drug effects | Cell Line, Tumor | Glucose - metabolism | Neurons - metabolism | Neurons - drug effects | Cytochrome c | Neurons | Resveratrol | Cytochrome oxidase | Mitochondrial DNA | Superoxide | Glucose | Dextrose | Index Medicus
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