Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 135, Issue 2, pp. 413 - 424.e15
Background Subsets of myeloid-derived regulatory cells (MDRCs), which are phenotypically similar to the myeloid-derived suppressor cells found in patients with...
Allergy and Immunology | macrophage | nitric oxide | regulatory T cell | superoxide | Myeloid cell | LUNG | POPULATION | superoxide regulatory T cell | ARGINASE | SUPEROXIDE-PRODUCTION | IMMUNOLOGY | CANCER | HYPERRESPONSIVENESS | ALLERGY | INFLAMMATION | NITRIC-OXIDE | SUPPRESSOR-CELLS | NITRATIVE STRESS | Reactive Oxygen Species - metabolism | Humans | Middle Aged | Bronchoalveolar Lavage Fluid - immunology | Male | Case-Control Studies | Forced Expiratory Volume | Myeloid Cells - immunology | Asthma - immunology | Antigens, Surface - metabolism | Free Radicals - metabolism | Adult | Female | Bronchoalveolar Lavage Fluid - cytology | Leukocyte Count | Asthma - diagnosis | Pulmonary Disease, Chronic Obstructive - diagnosis | Diagnosis, Differential | Immunomodulation | Risk Factors | Cell Communication | Immunophenotyping | Phenotype | Myeloid Cells - metabolism | T-Lymphocytes - immunology | Pulmonary Disease, Chronic Obstructive - immunology | Autoimmunity | Analysis | Asthma | Free radicals | Disease | Metabolites | Lymphocytes | Rodents | Population | Chronic obstructive pulmonary disease | Drug therapy | Inflammatory diseases
Allergy and Immunology | macrophage | nitric oxide | regulatory T cell | superoxide | Myeloid cell | LUNG | POPULATION | superoxide regulatory T cell | ARGINASE | SUPEROXIDE-PRODUCTION | IMMUNOLOGY | CANCER | HYPERRESPONSIVENESS | ALLERGY | INFLAMMATION | NITRIC-OXIDE | SUPPRESSOR-CELLS | NITRATIVE STRESS | Reactive Oxygen Species - metabolism | Humans | Middle Aged | Bronchoalveolar Lavage Fluid - immunology | Male | Case-Control Studies | Forced Expiratory Volume | Myeloid Cells - immunology | Asthma - immunology | Antigens, Surface - metabolism | Free Radicals - metabolism | Adult | Female | Bronchoalveolar Lavage Fluid - cytology | Leukocyte Count | Asthma - diagnosis | Pulmonary Disease, Chronic Obstructive - diagnosis | Diagnosis, Differential | Immunomodulation | Risk Factors | Cell Communication | Immunophenotyping | Phenotype | Myeloid Cells - metabolism | T-Lymphocytes - immunology | Pulmonary Disease, Chronic Obstructive - immunology | Autoimmunity | Analysis | Asthma | Free radicals | Disease | Metabolites | Lymphocytes | Rodents | Population | Chronic obstructive pulmonary disease | Drug therapy | Inflammatory diseases
Journal Article
Cellular and Molecular Neurobiology, ISSN 0272-4340, 07/2017, Volume 37, Issue 5, pp. 919 - 929
The CD4(+)CD25(+) regulatory T cells (Tregs), an innate immunomodulator, suppress cerebral inflammation and maintain immune homeostasis in multiple central...
Neurological deficits | Pro-inflammatory cytokines | Regulatory T cells | Intracerebral hemorrhage | ACTIVATION | IMMUNE HOMEOSTASIS | BRAIN-INJURY | ALPHA | EXPERIMENTAL STROKE | MECHANISMS | KAPPA-B | NEUROSCIENCES | CELL BIOLOGY | SIGNALING PATHWAY | EDEMA | CEREBRAL-ISCHEMIA | Malondialdehyde - metabolism | Inflammation - pathology | Cytokines - metabolism | Mice, Inbred C57BL | Male | Adoptive Transfer | Cerebral Hemorrhage - immunology | Hematoma - complications | T-Lymphocytes, Regulatory - immunology | Blood-Brain Barrier - pathology | Animals | Transcription Factor RelA - metabolism | Hematoma - pathology | Cerebral Hemorrhage - therapy | Hematoma - therapy | Hematoma - immunology | Cerebral Hemorrhage - pathology | Superoxide Dismutase - metabolism | Apoptosis | Disease Models, Animal | Yuan (China) | Enzymes | Brain | Interleukins | Analysis | Superoxide | Inflammation | T cells | Cells | Injuries
Neurological deficits | Pro-inflammatory cytokines | Regulatory T cells | Intracerebral hemorrhage | ACTIVATION | IMMUNE HOMEOSTASIS | BRAIN-INJURY | ALPHA | EXPERIMENTAL STROKE | MECHANISMS | KAPPA-B | NEUROSCIENCES | CELL BIOLOGY | SIGNALING PATHWAY | EDEMA | CEREBRAL-ISCHEMIA | Malondialdehyde - metabolism | Inflammation - pathology | Cytokines - metabolism | Mice, Inbred C57BL | Male | Adoptive Transfer | Cerebral Hemorrhage - immunology | Hematoma - complications | T-Lymphocytes, Regulatory - immunology | Blood-Brain Barrier - pathology | Animals | Transcription Factor RelA - metabolism | Hematoma - pathology | Cerebral Hemorrhage - therapy | Hematoma - therapy | Hematoma - immunology | Cerebral Hemorrhage - pathology | Superoxide Dismutase - metabolism | Apoptosis | Disease Models, Animal | Yuan (China) | Enzymes | Brain | Interleukins | Analysis | Superoxide | Inflammation | T cells | Cells | Injuries
Journal Article
Journal of Immunology, ISSN 0022-1767, 12/2012, Volume 189, Issue 11, pp. 5171 - 5177
Immunotherapy is a promising antitumor strategy that can successfully be combined with current anticancer treatment. In this study, arsenic trioxide (As2O3)...
NADPH OXIDASE | APOPTOSIS | CYCLOPHOSPHAMIDE | LEUKEMIA-CELLS | TUMOR | MICE | ERADICATION | IMMUNOLOGY | CYTOTOXICITY | ADOPTIVE IMMUNOTHERAPY | THERAPEUTIC AGENT | Reactive Oxygen Species - metabolism | CD8-Positive T-Lymphocytes - transplantation | Colonic Neoplasms - drug therapy | Humans | Oxidative Stress - immunology | Nitric Oxide Synthase - antagonists & inhibitors | Superoxide Dismutase - antagonists & inhibitors | Lymphocyte Depletion | Metalloporphyrins - pharmacology | T-Lymphocytes, Regulatory - pathology | T-Lymphocytes, Regulatory - immunology | Neoplasms, Experimental - pathology | Colonic Neoplasms - immunology | Neoplasms, Experimental - immunology | Female | Superoxide Dismutase - metabolism | NG-Nitroarginine Methyl Ester - pharmacology | Immunotherapy, Adoptive | Lymphocyte Activation | Reactive Nitrogen Species - metabolism | Arsenicals - pharmacology | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Fluoresceins | Oxides - pharmacology | T-Lymphocytes, Regulatory - drug effects | Animals | Colonic Neoplasms - pathology | Fluorescein | Mice | Nitric Oxide Synthase - metabolism | CD8-Positive T-Lymphocytes - immunology | Neoplasms, Experimental - drug therapy
NADPH OXIDASE | APOPTOSIS | CYCLOPHOSPHAMIDE | LEUKEMIA-CELLS | TUMOR | MICE | ERADICATION | IMMUNOLOGY | CYTOTOXICITY | ADOPTIVE IMMUNOTHERAPY | THERAPEUTIC AGENT | Reactive Oxygen Species - metabolism | CD8-Positive T-Lymphocytes - transplantation | Colonic Neoplasms - drug therapy | Humans | Oxidative Stress - immunology | Nitric Oxide Synthase - antagonists & inhibitors | Superoxide Dismutase - antagonists & inhibitors | Lymphocyte Depletion | Metalloporphyrins - pharmacology | T-Lymphocytes, Regulatory - pathology | T-Lymphocytes, Regulatory - immunology | Neoplasms, Experimental - pathology | Colonic Neoplasms - immunology | Neoplasms, Experimental - immunology | Female | Superoxide Dismutase - metabolism | NG-Nitroarginine Methyl Ester - pharmacology | Immunotherapy, Adoptive | Lymphocyte Activation | Reactive Nitrogen Species - metabolism | Arsenicals - pharmacology | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Fluoresceins | Oxides - pharmacology | T-Lymphocytes, Regulatory - drug effects | Animals | Colonic Neoplasms - pathology | Fluorescein | Mice | Nitric Oxide Synthase - metabolism | CD8-Positive T-Lymphocytes - immunology | Neoplasms, Experimental - drug therapy
Journal Article
JAMA Neurology, ISSN 2168-6149, 06/2018, Volume 75, Issue 6, p. 681
Importance Neuroinflammation appears to be a key modulator of disease progression in amyotrophic lateral sclerosis (ALS) and thereby a promising therapeutic...
Neuroprotection | Spinal cord | Animal models | Interleukin | Central nervous system | Peripheral nerves | Research facilities | Superoxide dismutase | Motors | Lymphocytes T | Activation | Neuronal-glial interactions | Cell activation | Immunology | Interleukin 2 | Rodents | Nerves | Biocompatibility | Foxp3 protein | Degeneration | Expansion | Data analysis | Therapeutic applications | Transgenic mice | Amyotrophic lateral sclerosis | Data processing | T cell receptors | Superoxide | Inflammation | Gene expression | Patients | Survival | Microglia | CD4 antigen | Amplification | Monoclonal antibodies | Mice | Cell size | Immunoreactivity
Neuroprotection | Spinal cord | Animal models | Interleukin | Central nervous system | Peripheral nerves | Research facilities | Superoxide dismutase | Motors | Lymphocytes T | Activation | Neuronal-glial interactions | Cell activation | Immunology | Interleukin 2 | Rodents | Nerves | Biocompatibility | Foxp3 protein | Degeneration | Expansion | Data analysis | Therapeutic applications | Transgenic mice | Amyotrophic lateral sclerosis | Data processing | T cell receptors | Superoxide | Inflammation | Gene expression | Patients | Survival | Microglia | CD4 antigen | Amplification | Monoclonal antibodies | Mice | Cell size | Immunoreactivity
Journal Article
APMIS, ISSN 0903-4641, 10/2017, Volume 125, Issue 10, pp. 888 - 901
The study was carried out to study expression of Toll like receptors 2 (TLR2), natural/inducible Treg and Interferon‐γ alongside oxidative stress and...
regulatory T cells | Celiac disease | Toll like receptor | oxidative stress | LIPID-PEROXIDATION | SUSCEPTIBILITY | TISSUE-DAMAGE | MICROBIOLOGY | IMMUNOLOGY | PATHOLOGY | CHILDREN | GLUTEN | INTERFERON-GAMMA | GLUTATHIONE | AUTOIMMUNITY | INFLAMMATION | SMALL-INTESTINAL MUCOSA | T-Lymphocyte Subsets - immunology | Superoxide Dismutase - analysis | Oxidative Stress | Humans | Male | T-Lymphocytes, Regulatory - immunology | Celiac Disease - pathology | Interferon-gamma - analysis | T-Lymphocyte Subsets - chemistry | Adolescent | Catalase - analysis | Toll-Like Receptor 2 - analysis | Female | T-Lymphocytes, Regulatory - chemistry | Lipid Peroxidation | Child | Oxidative stress | Interferon | T cells | Analysis | Glutathione peroxidase | Enzymes | Cytokines | Lipid peroxidation | Lipids | Lymphocytes T | Inflammation | Receptors | Catalase | Lymphocytes | Correlation analysis | TLR2 protein | Peripheral blood | Toll-like receptors | Peroxidase | Autoimmune diseases | Gluten | Glutathione
regulatory T cells | Celiac disease | Toll like receptor | oxidative stress | LIPID-PEROXIDATION | SUSCEPTIBILITY | TISSUE-DAMAGE | MICROBIOLOGY | IMMUNOLOGY | PATHOLOGY | CHILDREN | GLUTEN | INTERFERON-GAMMA | GLUTATHIONE | AUTOIMMUNITY | INFLAMMATION | SMALL-INTESTINAL MUCOSA | T-Lymphocyte Subsets - immunology | Superoxide Dismutase - analysis | Oxidative Stress | Humans | Male | T-Lymphocytes, Regulatory - immunology | Celiac Disease - pathology | Interferon-gamma - analysis | T-Lymphocyte Subsets - chemistry | Adolescent | Catalase - analysis | Toll-Like Receptor 2 - analysis | Female | T-Lymphocytes, Regulatory - chemistry | Lipid Peroxidation | Child | Oxidative stress | Interferon | T cells | Analysis | Glutathione peroxidase | Enzymes | Cytokines | Lipid peroxidation | Lipids | Lymphocytes T | Inflammation | Receptors | Catalase | Lymphocytes | Correlation analysis | TLR2 protein | Peripheral blood | Toll-like receptors | Peroxidase | Autoimmune diseases | Gluten | Glutathione
Journal Article
International Immunopharmacology, ISSN 1567-5769, 11/2018, Volume 64, pp. 208 - 216
The feature of pulmonary sarcoidosis is characterized by a Th1/Th17/regulatory T cells (Tregs) -driven inflammatory process in lung, resulting in noncaseating...
Interleukin 33 | Sarcoidosis | Regulatory T cell | PI3K/Akt | FOXP3 EXPRESSION | IMMUNITY | IL-33 PROMOTES | INNATE LYMPHOID-CELLS | IMMUNOLOGY | ATOPIC-DERMATITIS | AMPHIREGULIN | GRANULOMA-FORMATION | INFLAMMATION | DISEASE | ASTHMA | PHARMACOLOGY & PHARMACY | Th1 Cells - drug effects | Sarcoidosis, Pulmonary - immunology | Interleukin-33 - pharmacology | Sarcoidosis, Pulmonary - drug therapy | Mice, Inbred C57BL | Transforming Growth Factor beta - physiology | Th2 Cells - immunology | Th1 Cells - immunology | Th2 Cells - drug effects | T-Lymphocytes, Regulatory - immunology | T-Lymphocytes, Regulatory - drug effects | Animals | Interleukin-23 - antagonists & inhibitors | Phosphatidylinositol 3-Kinases - physiology | Female | Mice | Viral antibodies | Interleukins | Analysis | Antibodies | Bone morphogenetic proteins | Respiratory agents | Superoxide | T cells | Transforming growth factors
Interleukin 33 | Sarcoidosis | Regulatory T cell | PI3K/Akt | FOXP3 EXPRESSION | IMMUNITY | IL-33 PROMOTES | INNATE LYMPHOID-CELLS | IMMUNOLOGY | ATOPIC-DERMATITIS | AMPHIREGULIN | GRANULOMA-FORMATION | INFLAMMATION | DISEASE | ASTHMA | PHARMACOLOGY & PHARMACY | Th1 Cells - drug effects | Sarcoidosis, Pulmonary - immunology | Interleukin-33 - pharmacology | Sarcoidosis, Pulmonary - drug therapy | Mice, Inbred C57BL | Transforming Growth Factor beta - physiology | Th2 Cells - immunology | Th1 Cells - immunology | Th2 Cells - drug effects | T-Lymphocytes, Regulatory - immunology | T-Lymphocytes, Regulatory - drug effects | Animals | Interleukin-23 - antagonists & inhibitors | Phosphatidylinositol 3-Kinases - physiology | Female | Mice | Viral antibodies | Interleukins | Analysis | Antibodies | Bone morphogenetic proteins | Respiratory agents | Superoxide | T cells | Transforming growth factors
Journal Article
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 11/2011, Volume 31, Issue 11, pp. 2534 - 2542
OBJECTIVE—We previously demonstrated that a reduced number of CD4CD25-regulatory T cells (Tregs) was associated with microvascular dysfunction in hypertension....
vascular biology vasodilation | hypertension | nitric oxide synthase | OXIDATIVE STRESS | SUPEROXIDE | DEPENDENT RELAXATION | vasodilation | RESISTANCE ARTERIES | VASCULAR DYSFUNCTION | RATS | vascular biology | ANGIOTENSIN-II | BLOOD-FLOW | II-INFUSED MICE | INFLAMMATION | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | T-Lymphocytes, Regulatory - metabolism | NADPH Oxidases - metabolism | Male | T-Lymphocytes, Regulatory - pathology | Endothelium, Vascular - physiology | T-Lymphocytes, Regulatory - immunology | Hypertension - chemically induced | Interleukin-10 - metabolism | Angiotensin II - adverse effects | Vasodilation - physiology | Disease Models, Animal | Vasodilator Agents - pharmacology | Acetylcholine - pharmacology | Mice, Inbred C57BL | NADPH Oxidases - antagonists & inhibitors | Cells, Cultured | Cell- and Tissue-Based Therapy | Hypertension - physiopathology | Hypertension - metabolism | Mice, Knockout | Microvessels - physiology | Animals | Interleukin-2 Receptor alpha Subunit - metabolism | Interleukin-10 - genetics | Mice | Vasodilation - drug effects | CD4 Antigens - metabolism
vascular biology vasodilation | hypertension | nitric oxide synthase | OXIDATIVE STRESS | SUPEROXIDE | DEPENDENT RELAXATION | vasodilation | RESISTANCE ARTERIES | VASCULAR DYSFUNCTION | RATS | vascular biology | ANGIOTENSIN-II | BLOOD-FLOW | II-INFUSED MICE | INFLAMMATION | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | T-Lymphocytes, Regulatory - metabolism | NADPH Oxidases - metabolism | Male | T-Lymphocytes, Regulatory - pathology | Endothelium, Vascular - physiology | T-Lymphocytes, Regulatory - immunology | Hypertension - chemically induced | Interleukin-10 - metabolism | Angiotensin II - adverse effects | Vasodilation - physiology | Disease Models, Animal | Vasodilator Agents - pharmacology | Acetylcholine - pharmacology | Mice, Inbred C57BL | NADPH Oxidases - antagonists & inhibitors | Cells, Cultured | Cell- and Tissue-Based Therapy | Hypertension - physiopathology | Hypertension - metabolism | Mice, Knockout | Microvessels - physiology | Animals | Interleukin-2 Receptor alpha Subunit - metabolism | Interleukin-10 - genetics | Mice | Vasodilation - drug effects | CD4 Antigens - metabolism
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 07/2018, Volume 128, Issue 7, pp. 3088 - 3101
The superoxide-generating enzyme Nox2 contributes to hypertension and cardiovascular remodeling triggered by activation of the renin-angiotensin system....
MEDICINE, RESEARCH & EXPERIMENTAL | NADPH OXIDASE | INDUCED HYPERTENSION | OXIDATIVE STRESS | INTERSTITIAL CARDIAC FIBROSIS | VASCULAR DYSFUNCTION | HEART-FAILURE | MICE | TRANSCRIPTION-FACTOR | NF-KAPPA-B | LUNG INFLAMMATION | Genetic aspects | Research | Cardiovascular diseases | Genetic regulation | Risk factors | Heart | Transcription | Helper cells | Lymphocytes T | Adoptive transfer | Renin | Lymphocytes | CYBB protein | CD25 antigen | Foxp3 protein | CD73 antigen | Angiotensin II | Heart failure | Hypertension | NF-κB protein | Cytokines | Immunoregulation | Cardiomyocytes | Superoxide | Inflammation | Roles | CD4 antigen | Coronary vessels | Angiotensin | Regulation
MEDICINE, RESEARCH & EXPERIMENTAL | NADPH OXIDASE | INDUCED HYPERTENSION | OXIDATIVE STRESS | INTERSTITIAL CARDIAC FIBROSIS | VASCULAR DYSFUNCTION | HEART-FAILURE | MICE | TRANSCRIPTION-FACTOR | NF-KAPPA-B | LUNG INFLAMMATION | Genetic aspects | Research | Cardiovascular diseases | Genetic regulation | Risk factors | Heart | Transcription | Helper cells | Lymphocytes T | Adoptive transfer | Renin | Lymphocytes | CYBB protein | CD25 antigen | Foxp3 protein | CD73 antigen | Angiotensin II | Heart failure | Hypertension | NF-κB protein | Cytokines | Immunoregulation | Cardiomyocytes | Superoxide | Inflammation | Roles | CD4 antigen | Coronary vessels | Angiotensin | Regulation
Journal Article
International Immunopharmacology, ISSN 1567-5769, 11/2018, Volume 64, p. 208
The feature of pulmonary sarcoidosis is characterized by a Th1/Th17/regulatory T cells (Tregs) -driven inflammatory process in lung, resulting in noncaseating...
TOR protein | Flow cytometry | Interleukin | Helper cells | Homeostasis | Effector cells | Fluorescence | Superoxide dismutase | AKT protein | Interleukin 23 | Lymphocytes T | Smad3 protein | Proteins | Signal transduction | Pathways | Lymphocytes | Smad2 protein | Disturbance | Peripheral blood | Respiratory therapy | Cytokines | Sarcoidosis | Immunoregulation | T cell receptors | Superoxide | Inflammation | 1-Phosphatidylinositol 3-kinase | CD4 antigen | Signaling | Lungs
TOR protein | Flow cytometry | Interleukin | Helper cells | Homeostasis | Effector cells | Fluorescence | Superoxide dismutase | AKT protein | Interleukin 23 | Lymphocytes T | Smad3 protein | Proteins | Signal transduction | Pathways | Lymphocytes | Smad2 protein | Disturbance | Peripheral blood | Respiratory therapy | Cytokines | Sarcoidosis | Immunoregulation | T cell receptors | Superoxide | Inflammation | 1-Phosphatidylinositol 3-kinase | CD4 antigen | Signaling | Lungs
Journal Article
Molecular Medicine Reports, ISSN 1791-2997, 2014, Volume 9, Issue 5, pp. 1998 - 2002
Ischemia reperfusion injury (IRI) occurs in almost every liver surgery and is associated with the reduction of the liver blood flow. Ischemia impairs liver...
Ischemic reperfusion injury | Regulatory T cells | Heat shock protein 27 | Liver | MEDICINE, RESEARCH & EXPERIMENTAL | ACUTE KIDNEY INJURY | APOPTOSIS | HEPATIC ISCHEMIA | PROTECTION | liver | REGENERATION | heat shock protein 27 | ischemic reperfusion injury | regulatory T cells | ONCOLOGY | MICE | CARBON-TETRACHLORIDE
Ischemic reperfusion injury | Regulatory T cells | Heat shock protein 27 | Liver | MEDICINE, RESEARCH & EXPERIMENTAL | ACUTE KIDNEY INJURY | APOPTOSIS | HEPATIC ISCHEMIA | PROTECTION | liver | REGENERATION | heat shock protein 27 | ischemic reperfusion injury | regulatory T cells | ONCOLOGY | MICE | CARBON-TETRACHLORIDE
Journal Article
The Journal of allergy and clinical immunology, ISSN 0091-6749, 2/2015, Volume 135, Issue 2, pp. 413 - 424.e15
Journal Article
Free Radical Research, ISSN 1071-5762, 2010, Volume 44, Issue 4, pp. 363 - 378
Abstract Hepatic stellate cells (HSC) are the major producers of collagen in the liver and their conversion from resting cells to a proliferating, contractile...
Glutathione system | thioredoxin system | liver fibrosis | reactive nitrogen species (RNS) | redox regulation | mitochondria | NADPH oxidase | protein kinases | hepatic stellate cells (HSC) | reactive oxygen species (ROS) | Mitochondria | Thioredoxin system | Reactive oxygen species (ROS) | Redox regulation | Hepatic stellate cells (HSC) | Liver fibrosis | Reactive nitrogen species (RNS) | Protein kinases | SIGNAL-TRANSDUCTION | LUNG ENDOTHELIAL-CELLS | REACTIVE OXYGEN | RAT-LIVER FIBROSIS | MANGANESE SUPEROXIDE-DISMUTASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEDIATED TYROSINE PHOSPHORYLATION | NECROSIS-FACTOR-ALPHA | THIOREDOXIN REDUCTASE | HYDROGEN-PEROXIDE | NADPH OXIDASE ACTIVATION | Protein Kinases - metabolism | Liver - pathology | Cell Proliferation | Liver - enzymology | Reactive Oxygen Species - metabolism | Oxidation-Reduction | Signal Transduction | Glutathione - metabolism | Humans | Hepatic Stellate Cells - enzymology | NADPH Oxidases - metabolism | Liver Cirrhosis - enzymology | Mitochondria, Liver - enzymology | Collagen - metabolism | Phenotype | Animals | Liver Cirrhosis - pathology | Thioredoxins - metabolism | Hepatic Stellate Cells - pathology | Apoptosis
Glutathione system | thioredoxin system | liver fibrosis | reactive nitrogen species (RNS) | redox regulation | mitochondria | NADPH oxidase | protein kinases | hepatic stellate cells (HSC) | reactive oxygen species (ROS) | Mitochondria | Thioredoxin system | Reactive oxygen species (ROS) | Redox regulation | Hepatic stellate cells (HSC) | Liver fibrosis | Reactive nitrogen species (RNS) | Protein kinases | SIGNAL-TRANSDUCTION | LUNG ENDOTHELIAL-CELLS | REACTIVE OXYGEN | RAT-LIVER FIBROSIS | MANGANESE SUPEROXIDE-DISMUTASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEDIATED TYROSINE PHOSPHORYLATION | NECROSIS-FACTOR-ALPHA | THIOREDOXIN REDUCTASE | HYDROGEN-PEROXIDE | NADPH OXIDASE ACTIVATION | Protein Kinases - metabolism | Liver - pathology | Cell Proliferation | Liver - enzymology | Reactive Oxygen Species - metabolism | Oxidation-Reduction | Signal Transduction | Glutathione - metabolism | Humans | Hepatic Stellate Cells - enzymology | NADPH Oxidases - metabolism | Liver Cirrhosis - enzymology | Mitochondria, Liver - enzymology | Collagen - metabolism | Phenotype | Animals | Liver Cirrhosis - pathology | Thioredoxins - metabolism | Hepatic Stellate Cells - pathology | Apoptosis
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 12/2015, Volume 89, pp. 1 - 7
Vascular reactive oxygen species (ROS) are known to be involved in atherosclerosis development and progression. NADPH oxidase 4 (Nox4) is a constitutively...
Reactive oxygen species | CXCL9 | NADPH Oxidase 4 | T regulatory cells | Atherosclerosis | LOCALIZATION | OXIDATIVE STRESS | ACTIVATION | SUPEROXIDE | BIOCHEMISTRY & MOLECULAR BIOLOGY | HYPERCHOLESTEROLEMIA | INDUCTION | RESPONSES | ENDOCRINOLOGY & METABOLISM | REGULATORY T-CELLS | NOX4 | REVEALS | Endothelium, Vascular - cytology | T-Lymphocytes, Regulatory - metabolism | Cell Proliferation | Reactive Oxygen Species - metabolism | Oxidative Stress | Atherosclerosis - genetics | Humans | NADPH Oxidases - metabolism | Male | Aorta - metabolism | Interferon-gamma - metabolism | Immunoenzyme Techniques | NADPH Oxidases - genetics | Female | Real-Time Polymerase Chain Reaction | Cytokines - blood | Atherosclerosis - pathology | Mice, Inbred C57BL | RNA, Messenger - genetics | Cells, Cultured | Mice, Transgenic | Reverse Transcriptase Polymerase Chain Reaction | Atherosclerosis - metabolism | Blotting, Western | Mice, Knockout | Animals | Endothelium, Vascular - metabolism | Apolipoproteins E - physiology | Mice | Aorta - cytology | Atherosclerosis - prevention & control | Oxidases | Genetic engineering | Biological response modifiers | T cells | Apolipoproteins | Cells | Cardiovascular agents | Interferon gamma | Endothelium | Proteins | atherosclerosis | reactive oxygen species
Reactive oxygen species | CXCL9 | NADPH Oxidase 4 | T regulatory cells | Atherosclerosis | LOCALIZATION | OXIDATIVE STRESS | ACTIVATION | SUPEROXIDE | BIOCHEMISTRY & MOLECULAR BIOLOGY | HYPERCHOLESTEROLEMIA | INDUCTION | RESPONSES | ENDOCRINOLOGY & METABOLISM | REGULATORY T-CELLS | NOX4 | REVEALS | Endothelium, Vascular - cytology | T-Lymphocytes, Regulatory - metabolism | Cell Proliferation | Reactive Oxygen Species - metabolism | Oxidative Stress | Atherosclerosis - genetics | Humans | NADPH Oxidases - metabolism | Male | Aorta - metabolism | Interferon-gamma - metabolism | Immunoenzyme Techniques | NADPH Oxidases - genetics | Female | Real-Time Polymerase Chain Reaction | Cytokines - blood | Atherosclerosis - pathology | Mice, Inbred C57BL | RNA, Messenger - genetics | Cells, Cultured | Mice, Transgenic | Reverse Transcriptase Polymerase Chain Reaction | Atherosclerosis - metabolism | Blotting, Western | Mice, Knockout | Animals | Endothelium, Vascular - metabolism | Apolipoproteins E - physiology | Mice | Aorta - cytology | Atherosclerosis - prevention & control | Oxidases | Genetic engineering | Biological response modifiers | T cells | Apolipoproteins | Cells | Cardiovascular agents | Interferon gamma | Endothelium | Proteins | atherosclerosis | reactive oxygen species
Journal Article
Mucosal Immunology, ISSN 1933-0219, 09/2011, Volume 4, Issue 5, pp. 503 - 518
Levels of reactive free radicals are elevated in the airway during asthmatic exacerbations, but their roles in the pathophysiology of asthma remain unclear. We...
MURINE MODEL | MILD ASTHMA | SUPEROXIDE | REACTIVE OXYGEN | INHIBITION | TUMOR-BEARING MICE | ARGINASE-I | NITRIC-OXIDE SYNTHASE | ALVEOLAR MACROPHAGES | IMMUNOLOGY | T-CELLS | Asthma - metabolism | Bronchial Hyperreactivity - immunology | Arginase - metabolism | NADPH Oxidases - metabolism | Adoptive Transfer | Chemokine CCL22 - metabolism | Signal Transduction - immunology | Lymphocyte Activation - immunology | T-Lymphocytes - metabolism | Myeloid Cells - immunology | Asthma - immunology | Free Radicals - metabolism | Pneumonia - immunology | Bronchial Hyperreactivity - metabolism | Lung - pathology | Mice, Inbred C57BL | Mice, Knockout | Animals | Myeloid Cells - metabolism | T-Lymphocytes - immunology | Mice | Myeloid Cells - pathology | Pneumonia - metabolism | Lung - immunology | Nitric Oxide Synthase Type II - metabolism
MURINE MODEL | MILD ASTHMA | SUPEROXIDE | REACTIVE OXYGEN | INHIBITION | TUMOR-BEARING MICE | ARGINASE-I | NITRIC-OXIDE SYNTHASE | ALVEOLAR MACROPHAGES | IMMUNOLOGY | T-CELLS | Asthma - metabolism | Bronchial Hyperreactivity - immunology | Arginase - metabolism | NADPH Oxidases - metabolism | Adoptive Transfer | Chemokine CCL22 - metabolism | Signal Transduction - immunology | Lymphocyte Activation - immunology | T-Lymphocytes - metabolism | Myeloid Cells - immunology | Asthma - immunology | Free Radicals - metabolism | Pneumonia - immunology | Bronchial Hyperreactivity - metabolism | Lung - pathology | Mice, Inbred C57BL | Mice, Knockout | Animals | Myeloid Cells - metabolism | T-Lymphocytes - immunology | Mice | Myeloid Cells - pathology | Pneumonia - metabolism | Lung - immunology | Nitric Oxide Synthase Type II - metabolism
Journal Article