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Gastroenterology, ISSN 0016-5085, 2014, Volume 146, Issue 7, pp. 1763 - 1774
Background & Aims The NACHT, LRR, and pyrin domain–containing protein 3 (NLRP3) inflammasome induces inflammation in response to organ injury, but little is... 
Gastroenterology and Hepatology | Innate Immune Response | Immune Regulation | Pancreas | Mouse Model | ACTIVATION | NLRP3 INFLAMMASOME | GPR81 | AGONISTS | GENE | TLR9 | MICE | HEPATOTOXICITY | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | SEVERITY | Liver - pathology | Inflammasomes - metabolism | Receptors, G-Protein-Coupled - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein | Humans | Male | NF-kappa B - metabolism | Monocytes - immunology | Lipopolysaccharides | Liver - immunology | Liver - drug effects | RNA Interference | Interleukin-1beta - metabolism | Toll-Like Receptors - drug effects | Anti-Inflammatory Agents - administration & dosage | Toll-Like Receptors - metabolism | Cytoprotection | Disease Models, Animal | Galactosamine | Chemical and Drug Induced Liver Injury - prevention & control | Anti-Inflammatory Agents - pharmacology | Down-Regulation | Liver - metabolism | Injections, Intraperitoneal | Pancreas - pathology | Pancreas - metabolism | Pancreas - immunology | Toll-Like Receptor 4 - metabolism | Chemical and Drug Induced Liver Injury - immunology | Monocytes - drug effects | Macrophages - metabolism | Signal Transduction - drug effects | Chemical and Drug Induced Liver Injury - metabolism | Sodium Lactate - pharmacology | beta-Arrestins | Mice | Receptors, G-Protein-Coupled - genetics | RNA, Small Interfering - metabolism | Monocytes - metabolism | Pancreatitis - prevention & control | Arrestins - metabolism | Dose-Response Relationship, Drug | Pancreatitis - genetics | Transfection | Inflammasomes - drug effects | Sodium Lactate - administration & dosage | Pancreatitis - immunology | Chemical and Drug Induced Liver Injury - pathology | Chemical and Drug Induced Liver Injury - etiology | Macrophages - immunology | Cell Line | Immunity, Innate - drug effects | Toll-Like Receptor 4 - drug effects | Mice, Inbred C57BL | Pancreas - drug effects | Chemical and Drug Induced Liver Injury - genetics | Pancreatitis - chemically induced | Animals | Carrier Proteins - metabolism | beta-Arrestin 2 | Inflammasomes - immunology | Macrophages - drug effects | Pancreatitis - pathology | Pancreatitis - metabolism | Ceruletide | Lactates | Gastrointestinal diseases | Inflammation
Journal Article
Journal Article
Journal of the American Heart Association, ISSN 2047-9980, 09/2016, Volume 5, Issue 9, p. n/a
Journal Article
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 10/2007, Volume 293, Issue 4, pp. 2210 - 2218
Targeting cannabinoid-2 (CB2) receptors with selective agonists may represent a novel therapeutic avenue in various inflammatory diseases, but the mechanisms by which CB2 activation exerts its anti-inflammatory effects... 
Adhesion molecules | Inflammation | RhoA | Endothelial activation | C-REACTIVE PROTEIN | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | MOLECULE EXPRESSION | ATHEROSCLEROSIS | NECROSIS-FACTOR-ALPHA | KNOCKOUT MICE | endothelial activation | CANNABINOID RECEPTORS | inflammation | adhesion molecules | NITRIC-OXIDE | THERAPEUTIC TARGETS | PERIPHERAL VASCULAR DISEASE | POTENTIAL ROLE | CB2 RECEPTOR ACTIVATION | Inflammation - chemically induced | Leukocyte Rolling - drug effects | Tumor Necrosis Factor-alpha - metabolism | Receptor, Cannabinoid, CB2 - agonists | Humans | Male | Monocytes - metabolism | NF-kappa B - metabolism | rhoA GTP-Binding Protein - metabolism | Aorta - metabolism | RNA, Messenger - metabolism | Receptor, Cannabinoid, CB2 - genetics | Coronary Vessels - metabolism | Lipopolysaccharides | Dose-Response Relationship, Drug | Inflammation - metabolism | Anti-Inflammatory Agents - therapeutic use | Chemokine CCL2 - metabolism | Disease Models, Animal | Coronary Vessels - drug effects | Anti-Inflammatory Agents - pharmacology | Endothelial Cells - metabolism | Aorta - drug effects | Mice, Inbred C57BL | Cells, Cultured | Cannabinoids - pharmacology | Monocytes - drug effects | Receptor, Cannabinoid, CB1 - metabolism | Receptor, Cannabinoid, CB2 - metabolism | Cannabinoids - therapeutic use | Intercellular Adhesion Molecule-1 - metabolism | Animals | Signal Transduction - drug effects | Inflammation - prevention & control | Mice | Vascular Cell Adhesion Molecule-1 - metabolism | Endothelial Cells - drug effects
Journal Article
PloS one, ISSN 1932-6203, 2012, Volume 7, Issue 5, p. e36831
.... We focused on the in vitro effects of MJ-29 on ER stress and mitochondria-dependent apoptotic death in WEHI-3 cells, and to hypothesize that MJ-29 might fully impair the orthotopic leukemic mice... 
PERMEABILITY TRANSITION PORE | IMMUNE-RESPONSE | ACUTE LYMPHOBLASTIC-LEUKEMIA | IN-VIVO | BIOLOGY | TUBULIN POLYMERIZATION | DEATH | ANTITUMOR-ACTIVITY | BINDING AGENTS | CANCER | BALB/C MICE | Leukocytes, Mononuclear - metabolism | Reactive Oxygen Species | Apoptosis - drug effects | Calcium - metabolism | Body Weight - drug effects | Male | Leukemia - metabolism | Antineoplastic Agents - administration & dosage | Antigens, CD - metabolism | Antineoplastic Agents - toxicity | Lymphocytes - immunology | Antineoplastic Agents - pharmacology | Macrophages - immunology | Quinazolinones - pharmacology | Cell Survival - drug effects | Unfolded Protein Response - drug effects | Phagocytosis - drug effects | Leukocytes, Mononuclear - drug effects | Endoplasmic Reticulum Stress - drug effects | Leukemia - drug therapy | Mitochondria - drug effects | Organ Size - drug effects | Animals | Signal Transduction - drug effects | Cell Cycle Checkpoints - drug effects | Lymphocytes - drug effects | Cell Line, Tumor | Macrophages - drug effects | Mice | Mice, Inbred BALB C | Leukemia - mortality | Chemotherapy | Immunotherapy | Leukemia | Calpain | B cells | Cancer | Apoptosis | Flow cytometry | Liver | Body weight | Red pulp | Intracellular signalling | Cytotoxicity | Macrophages | Drug resistance | Cancer therapies | Pulp | Proteins | Mitochondria | Animal tissues | Cell cycle | Life sciences | Quinazolinone | Deoxyribonucleic acid--DNA | Spleen | Stresses | Myelomonocytic leukemia | Immune response | Calcium (intracellular) | Permeability | Stress | Cytometry | Monocytes | Lymphocytes B | Infiltration | Annexin V | Endoplasmic reticulum | Pharmaceuticals | Deoxyribonucleic acid | DNA
Journal Article
The Journal of experimental medicine, ISSN 1540-9538, 2008, Volume 205, Issue 4, pp. 869 - 882
Journal Article
Journal of Leukocyte Biology, ISSN 0741-5400, 12/2012, Volume 92, Issue 6, pp. 1147 - 1154
Journal Article
Journal of Periodontology, ISSN 0022-3492, 06/2014, Volume 85, Issue 6, pp. e212 - e223
Journal Article
The Journal of biological chemistry, ISSN 1083-351X, 2017, Volume 292, Issue 28, pp. 11682 - 11701
HIV-1 infection causes AIDS, infecting millions worldwide. The virus can persist in a state of chronic infection due to its ability to become latent. We have... 
ESCRT-II | HEPATITIS-C VIRUS | EXTRACELLULAR VESICLES | BIOCHEMISTRY & MOLECULAR BIOLOGY | MATRIX PROTEIN | IMMUNE ACTIVATION | HUMAN-IMMUNODEFICIENCY-VIRUS | GENOMIC RNA | TYPE-1 | EXPRESSION | CURRENT KNOWLEDGE | Exosomes - drug effects | Transcription, Genetic - drug effects | Monocytes - cytology | Humans | Endosomal Sorting Complexes Required for Transport - genetics | Monocytes - immunology | Ultracentrifugation | RNA Polymerase II - metabolism | Promoter Regions, Genetic - drug effects | Leukocytes, Mononuclear - virology | Virus Latency - drug effects | Exocytosis - drug effects | T-Lymphocytes - virology | HIV-1 - physiology | RNA Interference | Cattle | Endosomal Sorting Complexes Required for Transport - antagonists & inhibitors | T-Lymphocytes - drug effects | Exosomes - physiology | Leukocytes, Mononuclear - immunology | Exosomes - immunology | RNA Polymerase II - chemistry | Cell Line | Leukocytes, Mononuclear - drug effects | Immunity, Innate - drug effects | HIV-1 - drug effects | Anti-Retroviral Agents - pharmacology | Cells, Cultured | Endosomal Sorting Complexes Required for Transport - metabolism | Monocytes - drug effects | Monocytes - virology | HIV-1 - immunology | Models, Immunological | Animals | Virus Activation - drug effects | T-Lymphocytes - cytology | Leukocytes, Mononuclear - cytology | T-Lymphocytes - immunology | exosome (vesicle) | endosomal sorting complexes required for transport (ESCRT) | Microbiology | human immunodeficiency virus (HIV) | T-cell | transcription | latency | monocyte | small interfering RNA (siRNA)
Journal Article
PloS one, ISSN 1932-6203, 2017, Volume 12, Issue 1, p. e0170814
Chemotherapy-induced peripheral neuropathy (CIPN) and associated neuropathic pain is a debilitating adverse effect of cancer treatment... 
MACROPHAGE INFILTRATION | PAIN | INDUCED MECHANICAL ALLODYNIA | MULTIDISCIPLINARY SCIENCES | REGULATORY T-CELLS | DORSAL-ROOT GANGLIA | SPINAL-CORD | NERVE INJURY | SENSORY NEURONS | SATELLITE GLIAL-CELLS | PACLITAXEL | Hyperalgesia - chemically induced | Neuralgia - genetics | Spleen - immunology | Chemokine CCL2 - immunology | Male | Spleen - drug effects | Activating Transcription Factor 3 - immunology | T-Lymphocytes, Regulatory - pathology | Hyperalgesia - pathology | T-Lymphocytes, Regulatory - immunology | Neurofilament Proteins - genetics | Neuralgia - immunology | Chemokine CCL3 - genetics | Microglia - pathology | Lymph Nodes - drug effects | Activating Transcription Factor 3 - genetics | Receptors, Purinergic P2Y12 - genetics | Gene Expression | Receptors, Purinergic P2Y12 - immunology | Mice, Transgenic | Lymph Nodes - immunology | Spinal Cord - immunology | Hyperalgesia - immunology | T-Lymphocytes, Regulatory - drug effects | Hyperalgesia - genetics | Ganglia, Spinal - pathology | Mice | CD8-Positive T-Lymphocytes - immunology | Ganglia, Spinal - drug effects | CD8-Positive T-Lymphocytes - pathology | Lymph Nodes - pathology | Spinal Cord - drug effects | Chemokine CCL3 - immunology | Sensory Receptor Cells - immunology | Neuralgia - pathology | Microglia - immunology | Antineoplastic Agents - adverse effects | Spinal Cord - pathology | Neuralgia - chemically induced | Neurofilament Proteins - immunology | Spleen - pathology | Ganglia, Spinal - immunology | Sensory Receptor Cells - pathology | Microglia - drug effects | Mice, Inbred C57BL | Paclitaxel - adverse effects | Chemokine CCL2 - genetics | Animals | Sensory Receptor Cells - drug effects | CD8-Positive T-Lymphocytes - drug effects | Organoplatinum Compounds - adverse effects | Usage | Chemotherapy | Care and treatment | Oxalic acid | Polyneuropathies | Research | Diagnosis | T cells | Cancer | Spinal cord | Neurosciences | CD8 antigen | Carbon tetrachloride | Interleukin | Central nervous system | Transgenic | Nervous system | Diabetic neuropathy | Lymphocytes T | Cerebrospinal fluid | Peripheral neuropathy | Macrophages | Lymph nodes | Proteins | Neurotoxicity | Interleukin 4 | Pain | Dorsal root ganglia | Lymphocytes | Rodents | Sensory neurons | Tumor necrosis factor-TNF | Horns | Dorsal horn | Peripheral nervous system | Pain sensitivity | Spleen | Pain perception | Immune response | Cytokines | Granulocyte-macrophage colony-stimulating factor | Hypersensitivity | CCL3 protein | Interleukin 12 | Inflammation | CCL4 protein | Microglia | CD4 antigen | Studies | White blood cells | TNF inhibitors | Infiltration | Chemokines | Monocyte chemoattractant protein 1
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 07/2017, Volume 18, Issue 7, p. 1394
...), which play important roles in the progression of sepsis. In this study, we investigated the effects and mechanism of a novel histone deacetylase (HDAC8) inhibitor, (E... 
Histone deacetylase | Endotoxemia | Matrix metalloproteinases-9 (MMP-9) | Lipopolysaccharide (LPS) | lipopolysaccharide (LPS) | ACETYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | endotoxemia | TRANSCRIPTION | NEUTROPHILS | POTENTIAL ROLES | histone deacetylase | CHEMISTRY, MULTIDISCIPLINARY | HISTONE DEACETYLASES | INNATE IMMUNE-RESPONSES | GENE-EXPRESSION | NF-KAPPA-B | ASSOCIATION | matrix metalloproteinases-9 (MMP-9) | SEVERE SEPSIS | Tumor Necrosis Factor-alpha - metabolism | Humans | Male | Monocytes - metabolism | NF-kappa B - metabolism | YY1 Transcription Factor - metabolism | Interleukin-6 | RNA, Messenger - biosynthesis | Sepsis - drug therapy | Matrix Metalloproteinase 9 - metabolism | THP-1 Cells - drug effects | Tubulin - metabolism | Histone Deacetylase 1 - drug effects | Acetylation | Repressor Proteins - metabolism | RNA, Messenger - drug effects | JNK Mitogen-Activated Protein Kinases - drug effects | Cell Survival - drug effects | Chromosomal Proteins, Non-Histone - metabolism | Cytokines - metabolism | Down-Regulation | Mice, Inbred C57BL | Cell Cycle Proteins - metabolism | Chondroitin Sulfate Proteoglycans - metabolism | Histone Deacetylases - metabolism | Cyclooxygenase 2 - drug effects | Tumor Necrosis Factor-alpha - pharmacology | p38 Mitogen-Activated Protein Kinases - drug effects | Animals | MAP Kinase Signaling System - drug effects | Cytokines - drug effects | Signal Transduction - drug effects | Lipopolysaccharides - pharmacology | Matrix Metalloproteinase 9 - drug effects | Histone Deacetylase Inhibitors - pharmacology | Histone Deacetylases - drug effects | Repressor Proteins - drug effects | Mice
Journal Article