Nature Methods, ISSN 1548-7091, 02/2017, Volume 14, Issue 3, pp. 228 - 232
We argue that the field of extracellular vesicle (EV) biology needs more transparent reporting to facilitate interpretation and replication of experiments. To...
CELLS | NEED | SAMPLE COLLECTION | SUBPOPULATIONS | MINIMUM INFORMATION | COMPLEXES | BIOCHEMICAL RESEARCH METHODS | EXOSOMES | PHENOTYPE | STANDARDS | RELEASE | Extracellular Vesicles - physiology | Biomedical Research | Databases, Bibliographic | Internationality | Medicine, Experimental | Medical research | Extracellular matrix | Cell organelles | Observations | Reporting | Knowledge base | Biology | Life Sciences
CELLS | NEED | SAMPLE COLLECTION | SUBPOPULATIONS | MINIMUM INFORMATION | COMPLEXES | BIOCHEMICAL RESEARCH METHODS | EXOSOMES | PHENOTYPE | STANDARDS | RELEASE | Extracellular Vesicles - physiology | Biomedical Research | Databases, Bibliographic | Internationality | Medicine, Experimental | Medical research | Extracellular matrix | Cell organelles | Observations | Reporting | Knowledge base | Biology | Life Sciences
Journal Article
Seminars in Thrombosis and Hemostasis, ISSN 0094-6176, 06/2014, Volume 40, Issue 4, pp. 422 - 430
Abstract Hemolytic uremic syndrome (HUS) is a rare, life-threatening disease characterized by thrombocytopenia, microangiopathic hemolytic anemia, and acute...
aHUS | complement | thrombotic microangiopathy | C3 CONVERTASE | FACTOR-I | COMPLEMENT FACTOR-H | INHIBITOR ECULIZUMAB | ALTERNATIVE PATHWAY | ENDOTHELIAL-CELLS | BINDING-AFFINITY | TERMINAL REGION | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | MEMBRANE COFACTOR PROTEIN | MOLECULAR-BASIS | Genetic Predisposition to Disease | Genetic Association Studies | Introns | Humans | Diacylglycerol Kinase - genetics | Thrombotic Microangiopathies - genetics | Autoantibodies - immunology | RNA Splicing | Complement Factor B - genetics | Complement System Proteins - genetics | Heterozygote | Mutation | Thrombomodulin - genetics | Complement Factor H - genetics | Atypical Hemolytic Uremic Syndrome - genetics | Complement C3 - genetics
aHUS | complement | thrombotic microangiopathy | C3 CONVERTASE | FACTOR-I | COMPLEMENT FACTOR-H | INHIBITOR ECULIZUMAB | ALTERNATIVE PATHWAY | ENDOTHELIAL-CELLS | BINDING-AFFINITY | TERMINAL REGION | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | MEMBRANE COFACTOR PROTEIN | MOLECULAR-BASIS | Genetic Predisposition to Disease | Genetic Association Studies | Introns | Humans | Diacylglycerol Kinase - genetics | Thrombotic Microangiopathies - genetics | Autoantibodies - immunology | RNA Splicing | Complement Factor B - genetics | Complement System Proteins - genetics | Heterozygote | Mutation | Thrombomodulin - genetics | Complement Factor H - genetics | Atypical Hemolytic Uremic Syndrome - genetics | Complement C3 - genetics
Journal Article
FRONTIERS IN IMMUNOLOGY, ISSN 1664-3224, 06/2019, Volume 10, p. 1288
Mesenchymal stem or stromal cells (MSC) have proven immunomodulatory properties toward B cell activation and induce regulatory B cells (Breg), through a dual...
Ev isolation | mesenchymal stromal cells | memory B cell | immunosuppression | IMMUNOLOGY | STROMAL CELLS | CHROMATOGRAPHY | exosome | regulatory B cell | MESENCHYMAL STEM-CELLS | Stem cells | B cells | Usage | Research | Gel permeation chromatography
Ev isolation | mesenchymal stromal cells | memory B cell | immunosuppression | IMMUNOLOGY | STROMAL CELLS | CHROMATOGRAPHY | exosome | regulatory B cell | MESENCHYMAL STEM-CELLS | Stem cells | B cells | Usage | Research | Gel permeation chromatography
Journal Article
Frontiers in Immunology, ISSN 1664-3224, 2014, Volume 5, p. 416
Organ transplantation is often the unique solution for organ failure. However, rejection is still an unsolved problem. Although acute rejection is well...
Graft survival | Extracellular vesicles | Tolerance | Transplantation immunology | Organ transplantation | Exosomes | Graft rejection | graft rejection | TOLEROGENIC DENDRITIC CELLS | extracellular vesicles | LONG-TERM SURVIVAL | REPERFUSION INJURY | graft survival | ALLOGRAFT SURVIVAL | IMMUNOLOGY | VERSUS-HOST-DISEASE | MESENCHYMAL STEM-CELLS | transplantation immunology | organ transplantation | exosomes | REGULATORY T-CELLS | NOVO KIDNEY-TRANSPLANTATION | PROTEOMIC ANALYSIS | PEPTIDE-BASED VACCINE | tolerance | Graft Rejection | Graft Survival | Organ Transplantation | Transplantation Immunology
Graft survival | Extracellular vesicles | Tolerance | Transplantation immunology | Organ transplantation | Exosomes | Graft rejection | graft rejection | TOLEROGENIC DENDRITIC CELLS | extracellular vesicles | LONG-TERM SURVIVAL | REPERFUSION INJURY | graft survival | ALLOGRAFT SURVIVAL | IMMUNOLOGY | VERSUS-HOST-DISEASE | MESENCHYMAL STEM-CELLS | transplantation immunology | organ transplantation | exosomes | REGULATORY T-CELLS | NOVO KIDNEY-TRANSPLANTATION | PROTEOMIC ANALYSIS | PEPTIDE-BASED VACCINE | tolerance | Graft Rejection | Graft Survival | Organ Transplantation | Transplantation Immunology
Journal Article
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Full Text
Extracellular vesicle isolation methods: rising impact of size-exclusion chromatography
CELLULAR AND MOLECULAR LIFE SCIENCES, ISSN 1420-682X, 06/2019, Volume 76, Issue 12, pp. 2369 - 2382
Extracellular vesicles (EVs) include a variety of nanosized vesicles released to the extracellular microenvironment by the vast majority of cells transferring...
CELLS | Purification | SUBPOPULATIONS | QUANTIFICATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | MICROVESICLES | Exosomes | IDENTIFICATION | Theranostics | CELL BIOLOGY | LIQUID-CHROMATOGRAPHY | ULTRAFILTRATION | BIOGENESIS | Isolation methods | SEPARATION | Nanomedicine | Usage | RNA | Analysis | Physiological aspects | Lipids | Research institutes | Methods | Cells | Chromatography | Blood proteins | Size exclusion chromatography | Intercellular signalling | Laboratories | Immunomodulation | MiRNA | Ultracentrifugation | mRNA | Ribonucleic acid--RNA | Electron microscopy | Proteins | Heterogeneity | Vesicles | Plasma proteins | Quality standards | Biomarkers | Scaling | Conditioning | Non-coding RNA
CELLS | Purification | SUBPOPULATIONS | QUANTIFICATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | MICROVESICLES | Exosomes | IDENTIFICATION | Theranostics | CELL BIOLOGY | LIQUID-CHROMATOGRAPHY | ULTRAFILTRATION | BIOGENESIS | Isolation methods | SEPARATION | Nanomedicine | Usage | RNA | Analysis | Physiological aspects | Lipids | Research institutes | Methods | Cells | Chromatography | Blood proteins | Size exclusion chromatography | Intercellular signalling | Laboratories | Immunomodulation | MiRNA | Ultracentrifugation | mRNA | Ribonucleic acid--RNA | Electron microscopy | Proteins | Heterogeneity | Vesicles | Plasma proteins | Quality standards | Biomarkers | Scaling | Conditioning | Non-coding RNA
Journal Article
Stem Cell Research and Therapy, ISSN 1757-6512, 01/2019, Volume 10, Issue 1, pp. 23 - 12
BackgroundThe uterus is a histologically dynamic organ, and the mechanisms coordinating its regeneration during the oestrous cycle and implantation are poorly...
Embryo implantation | Inflammation | Endometrial mesenchymal stem cells | Cell migration | MEDICINE, RESEARCH & EXPERIMENTAL | STEM-CELLS | IMMUNE-SYSTEM | DECIDUALIZATION | MODEL | PREGNANCY | CELL BIOLOGY | Research | Cell differentiation | Gene expression | Epithelial cells | Stem cells | Vimentin | Cell proliferation | Tropism | Alkaline phosphatase | Mesenchyme | Oct-4 protein | Lymphocytes T | Metastasis | Estrus cycle | Phosphatase | Cell surface | Cell adhesion & migration | Cell growth | Uterus | Cattle | CD44 antigen | Fibroblasts | Tumor necrosis factor-TNF | Oviduct | Endometrium | Immune system | CD34 antigen | Estrus | Cytokines | Immunomodulation | Implantation | Tumor necrosis factor-α | Pregnancy | Immortalization | Cell lines | Interferon
Embryo implantation | Inflammation | Endometrial mesenchymal stem cells | Cell migration | MEDICINE, RESEARCH & EXPERIMENTAL | STEM-CELLS | IMMUNE-SYSTEM | DECIDUALIZATION | MODEL | PREGNANCY | CELL BIOLOGY | Research | Cell differentiation | Gene expression | Epithelial cells | Stem cells | Vimentin | Cell proliferation | Tropism | Alkaline phosphatase | Mesenchyme | Oct-4 protein | Lymphocytes T | Metastasis | Estrus cycle | Phosphatase | Cell surface | Cell adhesion & migration | Cell growth | Uterus | Cattle | CD44 antigen | Fibroblasts | Tumor necrosis factor-TNF | Oviduct | Endometrium | Immune system | CD34 antigen | Estrus | Cytokines | Immunomodulation | Implantation | Tumor necrosis factor-α | Pregnancy | Immortalization | Cell lines | Interferon
Journal Article
Frontiers in Immunology, ISSN 1664-3224, 11/2017, Volume 8, p. 1577
The ectoenzymes CD39 and CD73 regulate the purinergic signaling through the hydrolysis of adenosine triphosphate (ATP)/ADP to AMP and to adenosine (Ado),...
Mesenchymal stem cell | Myocardial infarction | Regeneration | Adenosine | CD73 | Immunomodulation | Purigernic signaling | Ectonucleotidase | immunomodulation | mesenchymal stem cell | FUNCTIONAL RECOVERY | ACTIVATION | DENDRITIC CELLS | MACROPHAGES | myocardial infarction | IMMUNOLOGY | adenosine | ADENOSINE A(2A) RECEPTORS | regenerationIN | REGULATORY T-CELLS | CD39 | GENERATION | purigernic signaling | STROMAL CELLS | ectonucleotidase | INHIBIT | Monocytes | Genetic aspects | Health aspects | Heart attack | Stem cells
Mesenchymal stem cell | Myocardial infarction | Regeneration | Adenosine | CD73 | Immunomodulation | Purigernic signaling | Ectonucleotidase | immunomodulation | mesenchymal stem cell | FUNCTIONAL RECOVERY | ACTIVATION | DENDRITIC CELLS | MACROPHAGES | myocardial infarction | IMMUNOLOGY | adenosine | ADENOSINE A(2A) RECEPTORS | regenerationIN | REGULATORY T-CELLS | CD39 | GENERATION | purigernic signaling | STROMAL CELLS | ectonucleotidase | INHIBIT | Monocytes | Genetic aspects | Health aspects | Heart attack | Stem cells
Journal Article
Scientific Reports, ISSN 2045-2322, 09/2016, Volume 6, Issue 1, p. 33641
Extracellular vesicles (EVs) have become an attractive field among the scientific community. Yet, a major challenge is to define a consensus method for EVs...
BIOMARKERS | EXOSOMES | PROTOCOL | DISEASES | MICROPARTICLES | MULTIDISCIPLINARY SCIENCES | Proteins | CD9 antigen | Vesicles | Plasma proteins | CD63 antigen | Polyethylene glycol | CD81 antigen | Ultracentrifugation | Electron microscopy | Chromatography
BIOMARKERS | EXOSOMES | PROTOCOL | DISEASES | MICROPARTICLES | MULTIDISCIPLINARY SCIENCES | Proteins | CD9 antigen | Vesicles | Plasma proteins | CD63 antigen | Polyethylene glycol | CD81 antigen | Ultracentrifugation | Electron microscopy | Chromatography
Journal Article
European Journal of Immunology, ISSN 0014-2980, 03/2017, Volume 47, Issue 3, pp. 504 - 515
C3 is the central component of the complement system. Upon activation, C3 sequentially generates various proteolytic fragments, C3a, C3b, iC3b, C3dg, each of...
C3b | Complement inhibition | Monoclonal antibody | C3bBb convertase | ACTIVATION | FACTOR-B | MECHANISM | ELECTRON-MICROSCOPY | FACTOR-H | 2 PARTS | PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA | IMMUNOLOGY | INHIBITION | ALTERNATIVE PATHWAY | DISEASE | Complement C3-C5 Convertases - metabolism | Immunoglobulin Fab Fragments - genetics | Complement C3 - metabolism | Humans | Complement C3 - immunology | Mice, Knockout | Antibodies, Monoclonal - genetics | Animals | Genetic Engineering | Hybridomas | Protein Binding | Protein Conformation | Mice | Antibodies, Monoclonal - metabolism | Antigen-Antibody Complex - metabolism | Complement Pathway, Alternative | Complement C3 - genetics | Hemolytic Plaque Technique | Proteins | Immunohistochemistry | Monoclonal antibodies | Health aspects
C3b | Complement inhibition | Monoclonal antibody | C3bBb convertase | ACTIVATION | FACTOR-B | MECHANISM | ELECTRON-MICROSCOPY | FACTOR-H | 2 PARTS | PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA | IMMUNOLOGY | INHIBITION | ALTERNATIVE PATHWAY | DISEASE | Complement C3-C5 Convertases - metabolism | Immunoglobulin Fab Fragments - genetics | Complement C3 - metabolism | Humans | Complement C3 - immunology | Mice, Knockout | Antibodies, Monoclonal - genetics | Animals | Genetic Engineering | Hybridomas | Protein Binding | Protein Conformation | Mice | Antibodies, Monoclonal - metabolism | Antigen-Antibody Complex - metabolism | Complement Pathway, Alternative | Complement C3 - genetics | Hemolytic Plaque Technique | Proteins | Immunohistochemistry | Monoclonal antibodies | Health aspects
Journal Article
BioMed Research International, ISSN 2314-6133, 2015, Volume 2015, pp. 439808 - 9
Cell-based strategies to regenerate injured myocardial tissue have emerged over the past decade, but the optimum cell type is still under scrutiny. In this...
MEDICINE, RESEARCH & EXPERIMENTAL | RESPONSES | IN-VITRO | THERAPY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | REGENERATION | DIFFERENTIATION | VERSUS-HOST-DISEASE | MARROW STROMAL CELLS | INHIBIT | LYMPHOCYTE-PROLIFERATION | TRANSPLANTATION | Fetal Blood - immunology | Stem Cells - immunology | Antibody Formation - immunology | Heart - physiology | Humans | Cells, Cultured | Immunologic Factors - immunology | Umbilical Cord - immunology | T-Lymphocytes - immunology | Adipose Tissue - immunology | Coculture Techniques - methods | Mesenchymal Stromal Cells - immunology | Adipose tissues | Cell interaction | T cells | Observations | Health aspects | Stem cells | Studies | Heart failure | Cytokines | Laboratories | Blood
MEDICINE, RESEARCH & EXPERIMENTAL | RESPONSES | IN-VITRO | THERAPY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | REGENERATION | DIFFERENTIATION | VERSUS-HOST-DISEASE | MARROW STROMAL CELLS | INHIBIT | LYMPHOCYTE-PROLIFERATION | TRANSPLANTATION | Fetal Blood - immunology | Stem Cells - immunology | Antibody Formation - immunology | Heart - physiology | Humans | Cells, Cultured | Immunologic Factors - immunology | Umbilical Cord - immunology | T-Lymphocytes - immunology | Adipose Tissue - immunology | Coculture Techniques - methods | Mesenchymal Stromal Cells - immunology | Adipose tissues | Cell interaction | T cells | Observations | Health aspects | Stem cells | Studies | Heart failure | Cytokines | Laboratories | Blood
Journal Article
CELL DEATH & DISEASE, ISSN 2041-4889, 05/2018, Volume 9, Issue 5, pp. 499 - 14
TLR sensing of pathogens triggers monocyte activation to initiate the host innate immune response to infection Monocytes can dynamically adapt to different TLR...
SIGNALING PATHWAYS | INFLUENZA-A VIRUS | DENDRITIC CELLS | INDUCIBLE GENE-I | HUMAN MACROPHAGES | TOLL-LIKE RECEPTORS | RIG-I | ACUTE-RENAL-FAILURE | INTRACELLULAR LPS | PATTERN-RECOGNITION RECEPTORS | CELL BIOLOGY | Tumor necrosis factor receptors | Antigen presentation | TLR7 protein | Immune response | Poly (I:C) | Inflammation | TLR4 protein | Tumor necrosis factor-α | Immunological tolerance | TLR3 protein | Lipopolysaccharides | Interleukin 6 | Monocytes | Cell activation | Cell death | Toll-like receptors | MyD88 protein | Apoptosis
SIGNALING PATHWAYS | INFLUENZA-A VIRUS | DENDRITIC CELLS | INDUCIBLE GENE-I | HUMAN MACROPHAGES | TOLL-LIKE RECEPTORS | RIG-I | ACUTE-RENAL-FAILURE | INTRACELLULAR LPS | PATTERN-RECOGNITION RECEPTORS | CELL BIOLOGY | Tumor necrosis factor receptors | Antigen presentation | TLR7 protein | Immune response | Poly (I:C) | Inflammation | TLR4 protein | Tumor necrosis factor-α | Immunological tolerance | TLR3 protein | Lipopolysaccharides | Interleukin 6 | Monocytes | Cell activation | Cell death | Toll-like receptors | MyD88 protein | Apoptosis
Journal Article
Clinical and Translational Allergy, ISSN 2045-7022, 11/2016, Volume 6, Issue S1
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 05/2016, Volume 27, Issue 5, pp. 1305 - 1311
The complement factor H (FH) mutation R1210C, which was described in association with atypical hemolytic uremic syndrome (aHUS), also confers high risk of...
Macular Degeneration - genetics | Pedigree | Complement C3 | Humans | Middle Aged | Female | Male | Mutation | Complement Factor H - genetics | Atypical Hemolytic Uremic Syndrome - genetics | Kidney Diseases - genetics | Kidney Glomerulus | glomerular disease | complement | hemolytic uremic syndrome | Brief Communications
Macular Degeneration - genetics | Pedigree | Complement C3 | Humans | Middle Aged | Female | Male | Mutation | Complement Factor H - genetics | Atypical Hemolytic Uremic Syndrome - genetics | Kidney Diseases - genetics | Kidney Glomerulus | glomerular disease | complement | hemolytic uremic syndrome | Brief Communications
Journal Article