Diabetes, ISSN 0012-1797, 05/2010, Volume 59, Issue 5, pp. 1171 - 1181
OBJECTIVE To identify, localize, and determine M1/M2 polarization of epidydimal adipose tissue (eAT) macrophages (Phi(S)) during high-fat diet (HFD)-induced...
ADIPOCYTE DEATH | PIOGLITAZONE | METABOLISM | INFLAMMATION | IN-VIVO | ENDOCRINOLOGY & METABOLISM | PPAR-GAMMA | MECHANISMS | ALTERNATIVE ACTIVATION | INDUCED INSULIN-RESISTANCE | ADIPOSE-TISSUE | Immunohistochemistry | Interleukin-12 Subunit p40 - metabolism | Dietary Fats - adverse effects | Obesity - chemically induced | Mice, Inbred C57BL | Receptors, Cell Surface - metabolism | Male | Obesity - physiopathology | Interleukin-13 - metabolism | Antigens, CD - metabolism | Obesity - metabolism | CD11c Antigen - metabolism | Adipose Tissue - metabolism | B7-2 Antigen - metabolism | Macrophages - metabolism | Animals | Flow Cytometry | Antigens, Differentiation, Myelomonocytic - metabolism | Interleukin 1 Receptor Antagonist Protein - metabolism | Polymerase Chain Reaction | Mice | Adipose tissues | Obesity | Complications and side effects | Dietary fat | Development and progression | Insulin resistance | Genetic aspects | Properties | Macrophages | Health aspects | Original
ADIPOCYTE DEATH | PIOGLITAZONE | METABOLISM | INFLAMMATION | IN-VIVO | ENDOCRINOLOGY & METABOLISM | PPAR-GAMMA | MECHANISMS | ALTERNATIVE ACTIVATION | INDUCED INSULIN-RESISTANCE | ADIPOSE-TISSUE | Immunohistochemistry | Interleukin-12 Subunit p40 - metabolism | Dietary Fats - adverse effects | Obesity - chemically induced | Mice, Inbred C57BL | Receptors, Cell Surface - metabolism | Male | Obesity - physiopathology | Interleukin-13 - metabolism | Antigens, CD - metabolism | Obesity - metabolism | CD11c Antigen - metabolism | Adipose Tissue - metabolism | B7-2 Antigen - metabolism | Macrophages - metabolism | Animals | Flow Cytometry | Antigens, Differentiation, Myelomonocytic - metabolism | Interleukin 1 Receptor Antagonist Protein - metabolism | Polymerase Chain Reaction | Mice | Adipose tissues | Obesity | Complications and side effects | Dietary fat | Development and progression | Insulin resistance | Genetic aspects | Properties | Macrophages | Health aspects | Original
Journal Article
Physiological Reviews, ISSN 0031-9333, 04/2008, Volume 88, Issue 2, pp. 389 - 419
The dramatic increase in the prevalence of obesity and its strong association with cardiovascular disease have resulted in unprecedented interest in...
OBSTRUCTIVE SLEEP-APNEA | PHYSIOLOGY | FATTY-ACID OXIDATION | ACTIVATED-RECEPTOR-GAMMA | SELECTIVE LEPTIN RESISTANCE | EPICARDIAL ADIPOSE-TISSUE | LEFT-VENTRICULAR MASS | CORONARY-HEART-DISEASE | TYPE-2 DIABETES-MELLITUS | INDUCED INSULIN-RESISTANCE | GLYCATION END-PRODUCTS | Heart - physiopathology | Animals | Humans | Myocardium - pathology | Obesity - physiopathology | Ventricular Remodeling - physiology | Adipokines - physiology | Disease Models, Animal | Obesity - pathology | Adipose tissues | Heart | Obesity | Analysis | Physiological aspects | Research | Cardiovascular diseases | Risk factors | Apoptosis
OBSTRUCTIVE SLEEP-APNEA | PHYSIOLOGY | FATTY-ACID OXIDATION | ACTIVATED-RECEPTOR-GAMMA | SELECTIVE LEPTIN RESISTANCE | EPICARDIAL ADIPOSE-TISSUE | LEFT-VENTRICULAR MASS | CORONARY-HEART-DISEASE | TYPE-2 DIABETES-MELLITUS | INDUCED INSULIN-RESISTANCE | GLYCATION END-PRODUCTS | Heart - physiopathology | Animals | Humans | Myocardium - pathology | Obesity - physiopathology | Ventricular Remodeling - physiology | Adipokines - physiology | Disease Models, Animal | Obesity - pathology | Adipose tissues | Heart | Obesity | Analysis | Physiological aspects | Research | Cardiovascular diseases | Risk factors | Apoptosis
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 06/2011, Volume 121, Issue 6, pp. 2094 - 2101
To fulfill its role as the major energy-storing tissue, adipose has several unique properties that cannot be seen in any other organ, including an almost...
MEDICINE, RESEARCH & EXPERIMENTAL | HYPOXIA-INDUCIBLE FACTOR | METABOLIC SYNDROME | FREE FATTY-ACIDS | IN-VIVO | NECROSIS-FACTOR-ALPHA | DIET-INDUCED OBESITY | CHRONIC INFLAMMATION | RECEPTOR TYROSINE KINASE | INDUCED INSULIN-RESISTANCE | ENDOTHELIAL GROWTH-FACTOR | Adaptation, Physiological | Macrophages - physiology | Macrophages - classification | Adipose Tissue - growth & development | Humans | Adipose Tissue - pathology | Adipose Tissue - physiopathology | Cell Size | Mice, Transgenic | Obesity - physiopathology | Adipocytes - physiology | Adipocytes - pathology | Cell Hypoxia | Animals | Adipose Tissue - blood supply | Cell Division | Extracellular Matrix - physiology | Weight Loss - physiology | Mice | Energy Metabolism - physiology | Fatty Acids - metabolism | Endothelial Cells - physiology | Neovascularization, Physiologic | Inflammation - physiopathology | Adipose tissues | Obesity | Review
MEDICINE, RESEARCH & EXPERIMENTAL | HYPOXIA-INDUCIBLE FACTOR | METABOLIC SYNDROME | FREE FATTY-ACIDS | IN-VIVO | NECROSIS-FACTOR-ALPHA | DIET-INDUCED OBESITY | CHRONIC INFLAMMATION | RECEPTOR TYROSINE KINASE | INDUCED INSULIN-RESISTANCE | ENDOTHELIAL GROWTH-FACTOR | Adaptation, Physiological | Macrophages - physiology | Macrophages - classification | Adipose Tissue - growth & development | Humans | Adipose Tissue - pathology | Adipose Tissue - physiopathology | Cell Size | Mice, Transgenic | Obesity - physiopathology | Adipocytes - physiology | Adipocytes - pathology | Cell Hypoxia | Animals | Adipose Tissue - blood supply | Cell Division | Extracellular Matrix - physiology | Weight Loss - physiology | Mice | Energy Metabolism - physiology | Fatty Acids - metabolism | Endothelial Cells - physiology | Neovascularization, Physiologic | Inflammation - physiopathology | Adipose tissues | Obesity | Review
Journal Article
The EMBO Journal, ISSN 0261-4189, 04/2011, Volume 30, Issue 8, pp. 1459 - 1472
Adipogenesis is tightly controlled by a complex network of transcription factors acting at different stages of differentiation. Peroxisome...
C/EBPβ | adipocyte differentiation | DNase I hypersensitivity | chromatin remodelling | ChIP‐seq | ChIP-seq | C/EBP beta | C/EBP-BETA | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | BINDING PROTEIN-BETA | HUMAN GENOME | GLUCOCORTICOID-RECEPTOR | IN-VIVO | ACTIVATED-RECEPTOR-GAMMA | PPAR-GAMMA | STIMULATES ADIPOGENESIS | ADIPOSE-TISSUE | CCAAT-Enhancer-Binding Protein-alpha - metabolism | Adipocytes - cytology | Adipogenesis - physiology | STAT5 Transcription Factor - genetics | STAT5 Transcription Factor - metabolism | Chromatin Immunoprecipitation | Tumor Suppressor Proteins - genetics | Transcription, Genetic | Cell Differentiation | Retinoid X Receptors - genetics | Retinoid X Receptors - metabolism | Tumor Suppressor Proteins - metabolism | CCAAT-Enhancer-Binding Protein-beta - genetics | RNA, Messenger - genetics | Chromatin Assembly and Disassembly | Transcription Factors - genetics | 3T3-L1 Cells | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | CCAAT-Enhancer-Binding Protein-beta - metabolism | Transcription Factors - metabolism | Algorithms | Animals | Adipocytes - metabolism | CCAAT-Enhancer-Binding Protein-alpha - genetics | Mice | Chromatin | Genes | Adipocytes | EBPβ
C/EBPβ | adipocyte differentiation | DNase I hypersensitivity | chromatin remodelling | ChIP‐seq | ChIP-seq | C/EBP beta | C/EBP-BETA | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | BINDING PROTEIN-BETA | HUMAN GENOME | GLUCOCORTICOID-RECEPTOR | IN-VIVO | ACTIVATED-RECEPTOR-GAMMA | PPAR-GAMMA | STIMULATES ADIPOGENESIS | ADIPOSE-TISSUE | CCAAT-Enhancer-Binding Protein-alpha - metabolism | Adipocytes - cytology | Adipogenesis - physiology | STAT5 Transcription Factor - genetics | STAT5 Transcription Factor - metabolism | Chromatin Immunoprecipitation | Tumor Suppressor Proteins - genetics | Transcription, Genetic | Cell Differentiation | Retinoid X Receptors - genetics | Retinoid X Receptors - metabolism | Tumor Suppressor Proteins - metabolism | CCAAT-Enhancer-Binding Protein-beta - genetics | RNA, Messenger - genetics | Chromatin Assembly and Disassembly | Transcription Factors - genetics | 3T3-L1 Cells | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | CCAAT-Enhancer-Binding Protein-beta - metabolism | Transcription Factors - metabolism | Algorithms | Animals | Adipocytes - metabolism | CCAAT-Enhancer-Binding Protein-alpha - genetics | Mice | Chromatin | Genes | Adipocytes | EBPβ
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 2014, Volume 55, Issue 4, pp. 739 - 746
The I148M substitution in patatin-like phospholipase domain containing 3 (PNPLA3(I148M)) determines a genetic form of nonalcoholic fatty liver disease. To...
Patatin-like phospholipase domain containing 3 | Adiponutrin | Lipidomics | Nonalcoholic fatty liver disease | Lipid droplet | Lipase | lipid droplet | patatin-like phospholipase domain containing 3 | FATTY LIVER-DISEASE | FAMILY-MEMBERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | lipase | INSULIN | adiponutrin | nonalcoholic fatty liver disease | ADIPONUTRIN/PNPLA3 GENE | TRIGLYCERIDE HYDROLYSIS | I148M | DOMAIN-CONTAINING 3 | HEPATIC STEATOSIS | EXPRESSION | lipidomics | ADIPOSE-TISSUE | Lipid Droplets - enzymology | Membrane Proteins - physiology | Humans | Cell Line, Tumor | Lipase - physiology | Lipid Metabolism | Mutation, Missense | Phospholipids - metabolism | Fatty Acids - metabolism | Hepatocytes - enzymology | Protein Transport | Triglycerides - metabolism
Patatin-like phospholipase domain containing 3 | Adiponutrin | Lipidomics | Nonalcoholic fatty liver disease | Lipid droplet | Lipase | lipid droplet | patatin-like phospholipase domain containing 3 | FATTY LIVER-DISEASE | FAMILY-MEMBERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | lipase | INSULIN | adiponutrin | nonalcoholic fatty liver disease | ADIPONUTRIN/PNPLA3 GENE | TRIGLYCERIDE HYDROLYSIS | I148M | DOMAIN-CONTAINING 3 | HEPATIC STEATOSIS | EXPRESSION | lipidomics | ADIPOSE-TISSUE | Lipid Droplets - enzymology | Membrane Proteins - physiology | Humans | Cell Line, Tumor | Lipase - physiology | Lipid Metabolism | Mutation, Missense | Phospholipids - metabolism | Fatty Acids - metabolism | Hepatocytes - enzymology | Protein Transport | Triglycerides - metabolism
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 01/2017, Volume 58, Issue 1, pp. 151 - 163
Mutations in the lamin A/C gene encoding nuclear lamins A and C (lamin A/C) cause familial partial lipodystrophy type 2 (FPLD2) and related lipodystrophy...
Adipose tissue | Supplementary adipocytes | Nuclear envelope | Fibrosis | METABOLIC SYNDROME | FAMILIAL PARTIAL LIPODYSTROPHY | BIOCHEMISTRY & MOLECULAR BIOLOGY | adipose tissue | nuclear envelope | MUSCULAR-DYSTROPHY | HUTCHINSON-GILFORD PROGERIA | DILATED CARDIOMYOPATHY | LMNA MUTATIONS | MANDIBULOACRAL DYSPLASIA | NUCLEAR LAMIN | fibrosis | C-TERMINAL DOMAIN | adipocytes | ADIPOSE-TISSUE | Cell Line | Matrix Metalloproteinase 9 - biosynthesis | Humans | Middle Aged | Adipose Tissue - pathology | Gene Expression Regulation | Lipodystrophy, Familial Partial - pathology | Extracellular Matrix - metabolism | Male | Lipodystrophy, Familial Partial - genetics | Transforming Growth Factor beta - biosynthesis | Mice, Knockout | Adipose Tissue - metabolism | Extracellular Matrix - genetics | Animals | Transforming Growth Factor beta - genetics | Matrix Metalloproteinase 9 - genetics | Lamin Type A - genetics | Aged, 80 and over | Aged | Mice | Mutation | Lipodystrophy, Familial Partial - metabolism | Transforming growth factor | Transgenic mice | Matrix metalloproteinase | Lamins | Insulin | C gene | Rodents | Fibroblasts | Lipodystrophy | Extracellular matrix | Metalloproteinase | Growth factors
Adipose tissue | Supplementary adipocytes | Nuclear envelope | Fibrosis | METABOLIC SYNDROME | FAMILIAL PARTIAL LIPODYSTROPHY | BIOCHEMISTRY & MOLECULAR BIOLOGY | adipose tissue | nuclear envelope | MUSCULAR-DYSTROPHY | HUTCHINSON-GILFORD PROGERIA | DILATED CARDIOMYOPATHY | LMNA MUTATIONS | MANDIBULOACRAL DYSPLASIA | NUCLEAR LAMIN | fibrosis | C-TERMINAL DOMAIN | adipocytes | ADIPOSE-TISSUE | Cell Line | Matrix Metalloproteinase 9 - biosynthesis | Humans | Middle Aged | Adipose Tissue - pathology | Gene Expression Regulation | Lipodystrophy, Familial Partial - pathology | Extracellular Matrix - metabolism | Male | Lipodystrophy, Familial Partial - genetics | Transforming Growth Factor beta - biosynthesis | Mice, Knockout | Adipose Tissue - metabolism | Extracellular Matrix - genetics | Animals | Transforming Growth Factor beta - genetics | Matrix Metalloproteinase 9 - genetics | Lamin Type A - genetics | Aged, 80 and over | Aged | Mice | Mutation | Lipodystrophy, Familial Partial - metabolism | Transforming growth factor | Transgenic mice | Matrix metalloproteinase | Lamins | Insulin | C gene | Rodents | Fibroblasts | Lipodystrophy | Extracellular matrix | Metalloproteinase | Growth factors
Journal Article
Cell, ISSN 0092-8674, 08/2012, Volume 150, Issue 3, pp. 620 - 632
Brown adipose tissue (BAT) can disperse stored energy as heat. Promoting BAT-like features in white adipose (WAT) is an attractive, if elusive, therapeutic...
THERMOGENESIS | OBESITY | ADIPOCYTES | METABOLISM | INSULIN-RESISTANCE | PGC-1-ALPHA | BIOCHEMISTRY & MOLECULAR BIOLOGY | ACTIVATED-RECEPTOR-GAMMA | FAT | MICE | SIRT1 | CELL BIOLOGY | Sirtuin 1 - metabolism | Humans | Adipose Tissue, White - metabolism | Molecular Sequence Data | Mice, 129 Strain | Stilbenes - pharmacology | PPAR gamma - metabolism | Sirtuin 1 - genetics | Adult | Female | Lysine - metabolism | Acetylation | Sirtuin 1 - chemistry | Thiazolidinediones - pharmacology | Lysine - analysis | Amino Acid Sequence | Mutagenesis, Site-Directed | Obesity - complications | Mice, Inbred C57BL | Cells, Cultured | Insulin Resistance | Models, Molecular | Obesity - metabolism | Sequence Alignment | Animals | Thermogenesis | Energy Metabolism | Ligands | Adipose Tissue, Brown - metabolism | Mice | Mutation | 3T3 Cells | PPAR gamma - chemistry
THERMOGENESIS | OBESITY | ADIPOCYTES | METABOLISM | INSULIN-RESISTANCE | PGC-1-ALPHA | BIOCHEMISTRY & MOLECULAR BIOLOGY | ACTIVATED-RECEPTOR-GAMMA | FAT | MICE | SIRT1 | CELL BIOLOGY | Sirtuin 1 - metabolism | Humans | Adipose Tissue, White - metabolism | Molecular Sequence Data | Mice, 129 Strain | Stilbenes - pharmacology | PPAR gamma - metabolism | Sirtuin 1 - genetics | Adult | Female | Lysine - metabolism | Acetylation | Sirtuin 1 - chemistry | Thiazolidinediones - pharmacology | Lysine - analysis | Amino Acid Sequence | Mutagenesis, Site-Directed | Obesity - complications | Mice, Inbred C57BL | Cells, Cultured | Insulin Resistance | Models, Molecular | Obesity - metabolism | Sequence Alignment | Animals | Thermogenesis | Energy Metabolism | Ligands | Adipose Tissue, Brown - metabolism | Mice | Mutation | 3T3 Cells | PPAR gamma - chemistry
Journal Article
Nature, ISSN 0028-0836, 05/2012, Volume 485, Issue 7398, pp. 391 - 395
Although feast and famine cycles illustrate that remodelling of adipose tissue in response to fluctuations in nutrient availability is essential for...
OBESITY | FIBROBLAST-GROWTH-FACTOR-1 | ADIPOCYTES | CAUSES INSULIN-RESISTANCE | TISSUE | BIOLOGY | MUSCLE | PPAR-GAMMA | FAT NECROSIS | FAMILY | MULTIDISCIPLINARY SCIENCES | Humans | Diabetes Mellitus, Experimental - genetics | Diet, High-Fat - adverse effects | Male | Fibroblast Growth Factor 1 - genetics | Adipocytes - drug effects | PPAR gamma - metabolism | Promoter Regions, Genetic - genetics | Base Sequence | Diabetes Mellitus, Experimental - chemically induced | Intra-Abdominal Fat - drug effects | Response Elements - genetics | Homeostasis - drug effects | Cell Size - drug effects | Mice, Inbred C57BL | Fibroblast Growth Factor 1 - metabolism | Insulin Resistance | Intra-Abdominal Fat - metabolism | Adipocytes - pathology | Fibroblast Growth Factor 1 - deficiency | Mice, Knockout | Insulin - metabolism | Animals | Adipocytes - metabolism | Diabetes Mellitus, Experimental - pathology | Inflammation - genetics | Mice | Intra-Abdominal Fat - pathology | Necrosis - enzymology | adipose remodelling | FGF1 | insulin resistance | PPARγ | Thiazolidinedione
OBESITY | FIBROBLAST-GROWTH-FACTOR-1 | ADIPOCYTES | CAUSES INSULIN-RESISTANCE | TISSUE | BIOLOGY | MUSCLE | PPAR-GAMMA | FAT NECROSIS | FAMILY | MULTIDISCIPLINARY SCIENCES | Humans | Diabetes Mellitus, Experimental - genetics | Diet, High-Fat - adverse effects | Male | Fibroblast Growth Factor 1 - genetics | Adipocytes - drug effects | PPAR gamma - metabolism | Promoter Regions, Genetic - genetics | Base Sequence | Diabetes Mellitus, Experimental - chemically induced | Intra-Abdominal Fat - drug effects | Response Elements - genetics | Homeostasis - drug effects | Cell Size - drug effects | Mice, Inbred C57BL | Fibroblast Growth Factor 1 - metabolism | Insulin Resistance | Intra-Abdominal Fat - metabolism | Adipocytes - pathology | Fibroblast Growth Factor 1 - deficiency | Mice, Knockout | Insulin - metabolism | Animals | Adipocytes - metabolism | Diabetes Mellitus, Experimental - pathology | Inflammation - genetics | Mice | Intra-Abdominal Fat - pathology | Necrosis - enzymology | adipose remodelling | FGF1 | insulin resistance | PPARγ | Thiazolidinedione
Journal Article
Circulation Research, ISSN 0009-7330, 02/2013, Volume 112, Issue 3, pp. 510 - 522
RATIONALE:The impact of diabetes mellitus on bone marrow (BM) structure is incompletely understood. OBJECTIVE:Investigate the effect of type-2 diabetes...
microangiopathy | stem cells | macroangiopathy | diabetes mellitus type 2 | bone marrow | CARDIAC & CARDIOVASCULAR SYSTEMS | TRANSCRIPTION | MICRORNAS | TRANSPLANTATION | HEART | ENDOTHELIAL PROGENITOR CELLS | DISEASE | PERIPHERAL VASCULAR DISEASE | COMPLICATIONS | NEOVASCULARIZATION | DIFFERENTIATION | HEMATOLOGY | EXPRESSION | Immunohistochemistry | Humans | Middle Aged | Microvessels - metabolism | Hematopoietic Stem Cells - pathology | Microvessels - pathology | Male | MicroRNAs - metabolism | Ischemia - genetics | Adipose Tissue - metabolism | Cyclin-Dependent Kinase Inhibitor p27 - metabolism | Forkhead Transcription Factors - metabolism | Bone Marrow Cells - immunology | Aged, 80 and over | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Ischemia - pathology | Biomarkers - metabolism | Peripheral Arterial Disease - metabolism | Stem Cell Niche | Signal Transduction | Endothelial Cells - metabolism | Adipose Tissue - pathology | Bone Marrow Cells - pathology | Bone Marrow Examination | Cell Lineage | MicroRNAs - genetics | Diabetes Mellitus, Type 2 - pathology | Endothelial Cells - pathology | Forkhead Box Protein O3 | Antigens, CD34 - metabolism | Peripheral Arterial Disease - pathology | Diabetes Mellitus, Type 2 - genetics | Diabetes Mellitus, Type 2 - metabolism | Microvessels - immunology | Case-Control Studies | Hematopoietic Stem Cells - immunology | Diabetic Angiopathies - pathology | Flow Cytometry | Transfection | Peripheral Arterial Disease - genetics | Adult | Female | Diabetic Angiopathies - genetics | Diabetic Angiopathies - metabolism | Cells, Cultured | Gene Expression Regulation | Ischemia - metabolism | Hematopoietic Stem Cells - metabolism | Forkhead Transcription Factors - genetics | Aged | Bone Marrow Cells - metabolism | Apoptosis
microangiopathy | stem cells | macroangiopathy | diabetes mellitus type 2 | bone marrow | CARDIAC & CARDIOVASCULAR SYSTEMS | TRANSCRIPTION | MICRORNAS | TRANSPLANTATION | HEART | ENDOTHELIAL PROGENITOR CELLS | DISEASE | PERIPHERAL VASCULAR DISEASE | COMPLICATIONS | NEOVASCULARIZATION | DIFFERENTIATION | HEMATOLOGY | EXPRESSION | Immunohistochemistry | Humans | Middle Aged | Microvessels - metabolism | Hematopoietic Stem Cells - pathology | Microvessels - pathology | Male | MicroRNAs - metabolism | Ischemia - genetics | Adipose Tissue - metabolism | Cyclin-Dependent Kinase Inhibitor p27 - metabolism | Forkhead Transcription Factors - metabolism | Bone Marrow Cells - immunology | Aged, 80 and over | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Ischemia - pathology | Biomarkers - metabolism | Peripheral Arterial Disease - metabolism | Stem Cell Niche | Signal Transduction | Endothelial Cells - metabolism | Adipose Tissue - pathology | Bone Marrow Cells - pathology | Bone Marrow Examination | Cell Lineage | MicroRNAs - genetics | Diabetes Mellitus, Type 2 - pathology | Endothelial Cells - pathology | Forkhead Box Protein O3 | Antigens, CD34 - metabolism | Peripheral Arterial Disease - pathology | Diabetes Mellitus, Type 2 - genetics | Diabetes Mellitus, Type 2 - metabolism | Microvessels - immunology | Case-Control Studies | Hematopoietic Stem Cells - immunology | Diabetic Angiopathies - pathology | Flow Cytometry | Transfection | Peripheral Arterial Disease - genetics | Adult | Female | Diabetic Angiopathies - genetics | Diabetic Angiopathies - metabolism | Cells, Cultured | Gene Expression Regulation | Ischemia - metabolism | Hematopoietic Stem Cells - metabolism | Forkhead Transcription Factors - genetics | Aged | Bone Marrow Cells - metabolism | Apoptosis
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 1/2016, Volume 73, Issue 2, pp. 349 - 363
Vascular remodeling is a dynamic process of structural and functional changes in response to biochemical and biomechanical signals in a complex in vivo milieu....
Life Sciences | Biochemistry, general | Vascular remodeling | Signal transduction | Reactive oxygen species | Life Sciences, general | Redox stress | Biomedicine general | Cell Biology | NADPH OXIDASE | OXIDATIVE STRESS | NITRIC-OXIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | OXYGEN SPECIES GENERATION | THIOREDOXIN-INTERACTING PROTEIN | ANGIOTENSIN-II | HYDROGEN-SULFIDE | CELL BIOLOGY | SIGNAL-TRANSDUCTION | SMOOTH-MUSCLE-CELLS | PERIVASCULAR ADIPOSE-TISSUE | Vascular Remodeling | Reactive Oxygen Species - metabolism | Oxidative Stress | Signal Transduction | Endothelial Cells - metabolism | Humans | Myocytes, Smooth Muscle - pathology | Homeostasis | Animals | Endothelial Cells - cytology | Nitric Oxide Synthase Type III - metabolism | Endothelial Cells - pathology | Myocytes, Smooth Muscle - cytology | Myocytes, Smooth Muscle - metabolism | Cardiology | Analysis | Cellular signal transduction | Cellular biology | Stress response
Life Sciences | Biochemistry, general | Vascular remodeling | Signal transduction | Reactive oxygen species | Life Sciences, general | Redox stress | Biomedicine general | Cell Biology | NADPH OXIDASE | OXIDATIVE STRESS | NITRIC-OXIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | OXYGEN SPECIES GENERATION | THIOREDOXIN-INTERACTING PROTEIN | ANGIOTENSIN-II | HYDROGEN-SULFIDE | CELL BIOLOGY | SIGNAL-TRANSDUCTION | SMOOTH-MUSCLE-CELLS | PERIVASCULAR ADIPOSE-TISSUE | Vascular Remodeling | Reactive Oxygen Species - metabolism | Oxidative Stress | Signal Transduction | Endothelial Cells - metabolism | Humans | Myocytes, Smooth Muscle - pathology | Homeostasis | Animals | Endothelial Cells - cytology | Nitric Oxide Synthase Type III - metabolism | Endothelial Cells - pathology | Myocytes, Smooth Muscle - cytology | Myocytes, Smooth Muscle - metabolism | Cardiology | Analysis | Cellular signal transduction | Cellular biology | Stress response
Journal Article