STEM CELLS, ISSN 1066-5099, 01/2019, Volume 37, Issue 1, pp. 14 - 25
The therapeutic potential of stem cell‐based therapies may be largely dependent on the ability of stem cells to modulate host cells rather than on their...
Organelle transfer | Mitochondria | Tunneling nanotubules | Stem cells | Lysosomes | Extracellular vesicles | Cellular fusion | Intercellular communication | MULTIPOTENT STROMAL CELLS | AXONAL-TRANSPORT | MITOCHONDRIAL TRANSFER | PLASMA-MEMBRANE | CUTTING EDGE | CELL & TISSUE ENGINEERING | CELL BIOLOGY | MEMBRANE NANOTUBES | IN-VITRO | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | TUNNELING NANOTUBES | ENDOTHELIAL-CELLS | HEMATOLOGY | Intercellular signalling | Therapeutic applications | Nanotubes | Organelles | Nanotechnology
Organelle transfer | Mitochondria | Tunneling nanotubules | Stem cells | Lysosomes | Extracellular vesicles | Cellular fusion | Intercellular communication | MULTIPOTENT STROMAL CELLS | AXONAL-TRANSPORT | MITOCHONDRIAL TRANSFER | PLASMA-MEMBRANE | CUTTING EDGE | CELL & TISSUE ENGINEERING | CELL BIOLOGY | MEMBRANE NANOTUBES | IN-VITRO | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | TUNNELING NANOTUBES | ENDOTHELIAL-CELLS | HEMATOLOGY | Intercellular signalling | Therapeutic applications | Nanotubes | Organelles | Nanotechnology
Journal Article
STEM CELLS, ISSN 1066-5099, 01/2019, Volume 37, Issue 1, pp. 14 - 25
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 11/2017, Volume 196, Issue 10, pp. 1275 - 1286
Litvack and colleagues also showed that, although not true AMs, stem cell-derived, alveolar-like macrophages improved bacterial and neutrophil clearance in...
Medical research | Oxidative stress | Pneumonia | Phosphorylation | Cytokines | Clinical trials | Inflammation | Studies | Genotype & phenotype | Mitochondria | Respiratory distress syndrome | Bioenergetics | Rodents | Stem cells | Bone marrow | Sepsis
Medical research | Oxidative stress | Pneumonia | Phosphorylation | Cytokines | Clinical trials | Inflammation | Studies | Genotype & phenotype | Mitochondria | Respiratory distress syndrome | Bioenergetics | Rodents | Stem cells | Bone marrow | Sepsis
Journal Article
STEM CELLS, ISSN 1066-5099, 08/2016, Volume 34, Issue 8, pp. 2210 - 2223
Mesenchymal stromal cells (MSC) have been reported to improve bacterial clearance in preclinical models of Acute Respiratory Distress Syndrome (ARDS) and...
Mitochondrial transfer | Macrophages | ARDS | Phagocytosis | Mesenchymal stem cells | SURVIVAL | ACUTE LUNG INJURY | SEPSIS | ORGANELLE TRANSFER | RESPIRATORY-DISTRESS-SYNDROME | CELL & TISSUE ENGINEERING | CELL BIOLOGY | MEMBRANE NANOTUBES | BACTERIAL CLEARANCE | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENDOTHELIAL-CELLS | MICE | STROMAL CELLS | HEMATOLOGY | Respiratory Distress Syndrome, Adult - pathology | Macrophages - pathology | Anti-Infective Agents - metabolism | Coculture Techniques | Humans | Cells, Cultured | Pneumonia - pathology | Cell Communication | Mesenchymal Stromal Cells - metabolism | Mitochondria - metabolism | Pneumonia - microbiology | Nanotubes - chemistry | Animals | Mice | Macrophages, Alveolar - metabolism | Escherichia coli - physiology | Neutrophils - metabolism | Disease Models, Animal | Acute respiratory distress syndrome | Pneumonia | Bacterial pneumonia | Stem cells | Nanotubes | Models | Mitochondrial DNA | Fish | Flow cytometry | Mesenchyme | Immune clearance | Fluorescence | Antiinfectives and antibacterials | Bisphosphonates | Blockage | Phagocytes | Mitochondria | Bioenergetics | E coli | Modulation | Imaging | Tunneling | Bacteria | Inhibition | Alveoli | Failure | Immune system | Clodronic acid | Flow | Cytometry | Monocytes | Depletion | Respiratory distress syndrome | Lungs | Stromal cells | Sepsis | In vivo methods and tests | In vitro methods and tests | Nanotechnology | Translational and Clinical Research
Mitochondrial transfer | Macrophages | ARDS | Phagocytosis | Mesenchymal stem cells | SURVIVAL | ACUTE LUNG INJURY | SEPSIS | ORGANELLE TRANSFER | RESPIRATORY-DISTRESS-SYNDROME | CELL & TISSUE ENGINEERING | CELL BIOLOGY | MEMBRANE NANOTUBES | BACTERIAL CLEARANCE | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENDOTHELIAL-CELLS | MICE | STROMAL CELLS | HEMATOLOGY | Respiratory Distress Syndrome, Adult - pathology | Macrophages - pathology | Anti-Infective Agents - metabolism | Coculture Techniques | Humans | Cells, Cultured | Pneumonia - pathology | Cell Communication | Mesenchymal Stromal Cells - metabolism | Mitochondria - metabolism | Pneumonia - microbiology | Nanotubes - chemistry | Animals | Mice | Macrophages, Alveolar - metabolism | Escherichia coli - physiology | Neutrophils - metabolism | Disease Models, Animal | Acute respiratory distress syndrome | Pneumonia | Bacterial pneumonia | Stem cells | Nanotubes | Models | Mitochondrial DNA | Fish | Flow cytometry | Mesenchyme | Immune clearance | Fluorescence | Antiinfectives and antibacterials | Bisphosphonates | Blockage | Phagocytes | Mitochondria | Bioenergetics | E coli | Modulation | Imaging | Tunneling | Bacteria | Inhibition | Alveoli | Failure | Immune system | Clodronic acid | Flow | Cytometry | Monocytes | Depletion | Respiratory distress syndrome | Lungs | Stromal cells | Sepsis | In vivo methods and tests | In vitro methods and tests | Nanotechnology | Translational and Clinical Research
Journal Article
STEM CELLS, ISSN 1066-5099, 08/2016, Volume 34, Issue 8, pp. 2210 - 2223
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 11/2017, Volume 196, Issue 10, pp. 1275 - 1286
Rationale: Acute respiratory distress syndrome (ARDS) remains a major cause of respiratory failure in critically ill patients. Mesenchymal stromal cells (MSCs)...
Acute respiratory distress syndrome | Extracellular vesicles | Mesenchymal stromal cells | Mitochondria | Macrophages | STEM-CELLS | extracellular vesicles | INTERNATIONAL-SOCIETY | VIVO | mitochondria | mesenchymal stromal cells | RESOLUTION | MICROVESICLES | INDUCTION | RESPIRATORY-DISTRESS-SYNDROME | macrophages | IN-VITRO | THERAPY | RESPIRATORY SYSTEM | acute respiratory distress syndrome | SECRETION | CRITICAL CARE MEDICINE | Acute Lung Injury - physiopathology | Acute Lung Injury - therapy | Humans | Male | Animals | Extracellular Vesicles - physiology | Female | Models, Animal | Mice | Macrophage-Activating Factors - therapeutic use | Mitochondria - physiology | Mesenchymal Stem Cell Transplantation | Mesenchymal Stromal Cells - physiology | Original
Acute respiratory distress syndrome | Extracellular vesicles | Mesenchymal stromal cells | Mitochondria | Macrophages | STEM-CELLS | extracellular vesicles | INTERNATIONAL-SOCIETY | VIVO | mitochondria | mesenchymal stromal cells | RESOLUTION | MICROVESICLES | INDUCTION | RESPIRATORY-DISTRESS-SYNDROME | macrophages | IN-VITRO | THERAPY | RESPIRATORY SYSTEM | acute respiratory distress syndrome | SECRETION | CRITICAL CARE MEDICINE | Acute Lung Injury - physiopathology | Acute Lung Injury - therapy | Humans | Male | Animals | Extracellular Vesicles - physiology | Female | Models, Animal | Mice | Macrophage-Activating Factors - therapeutic use | Mitochondria - physiology | Mesenchymal Stem Cell Transplantation | Mesenchymal Stromal Cells - physiology | Original
Journal Article
Bio-protocol, ISSN 2331-8325, 05/2017, Volume 7, Issue 9
Mesenchymal stem/stromal cells (MSC) are adult stem cells which have been shown to improve survival, enhance bacterial clearance and alleviate inflammation in...
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Expression pattern of arenicins-the antimicrobial peptides of polychaete Arenicola marina
Frontiers in Physiology, ISSN 1664-042X, 2014, Volume 5, p. 497
Immune responses of invertebrate animals are mediated through innate mechanisms, among which production of antimicrobial peptides play an important role....
Arenicola marina | Coelomocytes | Annelid | Invertebrate immunity | Antimicrobial peptides | CELLS | ANTIBACTERIAL PEPTIDES | PHYSIOLOGY | DEFENSINS | annelid | EXTRAVASAL TISSUE | CHALLENGE | invertebrate immunity | PURIFICATION | coelomocytes | HEART-BODY | PROMOTES | antimicrobial peptides | LEECH
Arenicola marina | Coelomocytes | Annelid | Invertebrate immunity | Antimicrobial peptides | CELLS | ANTIBACTERIAL PEPTIDES | PHYSIOLOGY | DEFENSINS | annelid | EXTRAVASAL TISSUE | CHALLENGE | invertebrate immunity | PURIFICATION | coelomocytes | HEART-BODY | PROMOTES | antimicrobial peptides | LEECH
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Frontiers in Physiology, ISSN 1664-042X, 12/2014, Volume 5
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10.
Full Text
Expression pattern of arenicins - the antimicrobial peptides of polychaete Arenicolamarina
Frontiers in Physiology, 12/2014, Volume 5
Immune responses of invertebrate animals are mediated through innate mechanisms, among which production of antimicrobial peptides play an important role....
Annelids | Arenicola marina | invertebrate immunity | coelomocytes | antimicrobial peptides
Annelids | Arenicola marina | invertebrate immunity | coelomocytes | antimicrobial peptides
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 04/2013, Volume 187, Issue 7, pp. 751 - 760
Rationale: Mesenchymal stem cells secrete paracrine factors that can regulate lung permeability and decrease inflammation, making it a potentially attractive...
Acute lung injury | Cell-based therapy | Keratinocyte growth factor | Bacterial pneumonia | PROGENITOR CELLS | keratinocyte growth factor | GROWTH-FACTOR PROTECTS | SEPSIS | acute lung injury | RESPIRATORY-DISTRESS-SYNDROME | INTRATRACHEAL INSTILLATION | ENGRAFTMENT | EPITHELIAL-CELLS | cell-based therapy | RESPIRATORY SYSTEM | bacterial pneumonia | MICE | STROMAL CELLS | EXPRESSION | CRITICAL CARE MEDICINE | Macrophages, Alveolar - microbiology | Receptor, Fibroblast Growth Factor, Type 2 - metabolism | Humans | Pneumonia, Bacterial - complications | Cells, Cultured | Phagocytosis - physiology | Mesenchymal Stromal Cells - secretion | Mesenchymal Stem Cell Transplantation - methods | Inflammation - therapy | Acute Lung Injury - microbiology | Analysis of Variance | Pulmonary Alveoli - metabolism | Fibroblast Growth Factor 7 - secretion | Acute Lung Injury - etiology | Escherichia coli Infections - complications
Acute lung injury | Cell-based therapy | Keratinocyte growth factor | Bacterial pneumonia | PROGENITOR CELLS | keratinocyte growth factor | GROWTH-FACTOR PROTECTS | SEPSIS | acute lung injury | RESPIRATORY-DISTRESS-SYNDROME | INTRATRACHEAL INSTILLATION | ENGRAFTMENT | EPITHELIAL-CELLS | cell-based therapy | RESPIRATORY SYSTEM | bacterial pneumonia | MICE | STROMAL CELLS | EXPRESSION | CRITICAL CARE MEDICINE | Macrophages, Alveolar - microbiology | Receptor, Fibroblast Growth Factor, Type 2 - metabolism | Humans | Pneumonia, Bacterial - complications | Cells, Cultured | Phagocytosis - physiology | Mesenchymal Stromal Cells - secretion | Mesenchymal Stem Cell Transplantation - methods | Inflammation - therapy | Acute Lung Injury - microbiology | Analysis of Variance | Pulmonary Alveoli - metabolism | Fibroblast Growth Factor 7 - secretion | Acute Lung Injury - etiology | Escherichia coli Infections - complications
Journal Article
FASEB JOURNAL, ISSN 0892-6638, 04/2019, Volume 33, Issue 4, pp. 5585 - 5598
Acute respiratory distress syndrome (ARDS) is a devastating disorder characterized by diffuse inflammation and edema formation. The main management strategy,...
MORTALITY | wound healing | BIOCHEMISTRY & MOLECULAR BIOLOGY | INJURY | CELL BIOLOGY | IN-VITRO | VENTILATION | MODELS | INFLAMMATION | hypercapnic acidosis | ENDOTHELIAL-CELLS | BIOLOGY | mitochondrial transfer | STROMAL CELLS | EXPRESSION | ARDS | CAVEOLIN-1 | Research
MORTALITY | wound healing | BIOCHEMISTRY & MOLECULAR BIOLOGY | INJURY | CELL BIOLOGY | IN-VITRO | VENTILATION | MODELS | INFLAMMATION | hypercapnic acidosis | ENDOTHELIAL-CELLS | BIOLOGY | mitochondrial transfer | STROMAL CELLS | EXPRESSION | ARDS | CAVEOLIN-1 | Research
Journal Article
STEM CELLS Translational Medicine, ISSN 2157-6564, 10/2019
Journal Article
Thorax, ISSN 0040-6376, 06/2012, Volume 67, Issue 6, pp. 533 - 539
RationaleBacterial pneumonia is the most common infectious cause of death worldwide and treatment is increasingly hampered by antibiotic resistance....
INTERLEUKIN-17 | RESPIRATORY SYSTEM | INFLAMMATION | INDUCED ACUTE LUNG | INJURY | MICE | INFECTION | GELATINASE-ASSOCIATED LIPOCALIN | TNF-ALPHA | SEPSIS | STROMAL CELLS | Lipocalins - biosynthesis | Lipocalins - metabolism | Up-Regulation | Pneumonia, Bacterial - microbiology | Escherichia coli Infections - surgery | Acute-Phase Proteins - metabolism | Mice, Inbred C57BL | Oncogene Proteins - metabolism | Treatment Outcome | Mesenchymal Stem Cell Transplantation - methods | Animals | Pneumonia, Bacterial - surgery | Lipocalin-2 | Escherichia coli - pathogenicity | Oncogene Proteins - biosynthesis | Survival Analysis | Mice | Trachea | Acute-Phase Proteins - biosynthesis | Escherichia coli Infections - complications | Disease Models, Animal
INTERLEUKIN-17 | RESPIRATORY SYSTEM | INFLAMMATION | INDUCED ACUTE LUNG | INJURY | MICE | INFECTION | GELATINASE-ASSOCIATED LIPOCALIN | TNF-ALPHA | SEPSIS | STROMAL CELLS | Lipocalins - biosynthesis | Lipocalins - metabolism | Up-Regulation | Pneumonia, Bacterial - microbiology | Escherichia coli Infections - surgery | Acute-Phase Proteins - metabolism | Mice, Inbred C57BL | Oncogene Proteins - metabolism | Treatment Outcome | Mesenchymal Stem Cell Transplantation - methods | Animals | Pneumonia, Bacterial - surgery | Lipocalin-2 | Escherichia coli - pathogenicity | Oncogene Proteins - biosynthesis | Survival Analysis | Mice | Trachea | Acute-Phase Proteins - biosynthesis | Escherichia coli Infections - complications | Disease Models, Animal
Journal Article
STEM CELLS, ISSN 1066-5099, 05/2018, Volume 36, Issue 5, pp. 796 - 806
Bone marrow derived mesenchymal stromal cells have been shown to have significant therapeutic effects in experimental models of pneumonia and lung injury. The...
Toll‐like receptor | Pneumonia | Protease‐activated receptor | Mesenchymal stem cells | Lung injury | Protease-activated receptor | Toll-like receptor | STEM-CELLS | ESCHERICHIA-COLI | ACUTE LUNG INJURY | E. COLI | CELL & TISSUE ENGINEERING | CELL BIOLOGY | CROSS-TALK | TOLL-LIKE | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | INFLAMMATION | IN-VIVO | COAGULATION | TNF-ALPHA | HEMATOLOGY | Bacterial pneumonia | Analysis | Escherichia coli | Stem cells | Thrombin | Health aspects | Animal models | Cell survival | Mesenchyme | Secretion | Stem cell transplantation | Cytotoxicity | Inflammation | TLR4 protein | Survival | Signal transduction | Signaling | Pathways | E coli | Lungs | Stromal cells | Bone marrow | Toll-like receptors | Prothrombin | In vivo methods and tests | protease-activated receptor | toll-like receptor | lung injury | pneumonia | mesenchymal stem cells
Toll‐like receptor | Pneumonia | Protease‐activated receptor | Mesenchymal stem cells | Lung injury | Protease-activated receptor | Toll-like receptor | STEM-CELLS | ESCHERICHIA-COLI | ACUTE LUNG INJURY | E. COLI | CELL & TISSUE ENGINEERING | CELL BIOLOGY | CROSS-TALK | TOLL-LIKE | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | INFLAMMATION | IN-VIVO | COAGULATION | TNF-ALPHA | HEMATOLOGY | Bacterial pneumonia | Analysis | Escherichia coli | Stem cells | Thrombin | Health aspects | Animal models | Cell survival | Mesenchyme | Secretion | Stem cell transplantation | Cytotoxicity | Inflammation | TLR4 protein | Survival | Signal transduction | Signaling | Pathways | E coli | Lungs | Stromal cells | Bone marrow | Toll-like receptors | Prothrombin | In vivo methods and tests | protease-activated receptor | toll-like receptor | lung injury | pneumonia | mesenchymal stem cells
Journal Article
STEM CELLS, ISSN 1066-5099, 06/2011, Volume 29, Issue 6, pp. 913 - 919
Morbidity and mortality have declined only modestly in patients with clinical acute lung injury (ALI) and acute respiratory distress syndrome (ARDS), despite...
Acute lung injury | Angiopoietin‐1 | Keratinocyte growth factor | LL‐37 | Pulmonary edema | Mesenchymal stem cells | Angiopoietin-1 | LL-37 | GROWTH-FACTOR PROTECTS | MYOCARDIAL-INFARCTION | BONE-MARROW | MULTIPOTENT STROMAL CELLS | RESPIRATORY-DISTRESS-SYNDROME | CELL & TISSUE ENGINEERING | CELL BIOLOGY | INTRATRACHEAL INSTILLATION | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | EPITHELIAL FLUID TRANSPORT | ANTIGEN-PRESENTING CELL | ANGIOPOIETIN-1 GENE-THERAPY | HEMATOLOGY | PULMONARY-EDEMA FLUID | Acute Lung Injury - physiopathology | Lung - pathology | Pneumonia, Bacterial - microbiology | Capillary Permeability | Paracrine Communication | Acute Lung Injury - therapy | Immunomodulation | Humans | Pneumonia, Bacterial - etiology | Mesenchymal Stromal Cells - metabolism | Clinical Trials as Topic | Lung - physiopathology | Acute Lung Injury - pathology | Mesenchymal Stem Cell Transplantation - adverse effects | Pneumonia, Bacterial - prevention & control | Mesenchymal Stromal Cells - immunology | Intercellular Signaling Peptides and Proteins - metabolism | Regeneration | Animals | Lung - metabolism | Disease Models, Animal
Acute lung injury | Angiopoietin‐1 | Keratinocyte growth factor | LL‐37 | Pulmonary edema | Mesenchymal stem cells | Angiopoietin-1 | LL-37 | GROWTH-FACTOR PROTECTS | MYOCARDIAL-INFARCTION | BONE-MARROW | MULTIPOTENT STROMAL CELLS | RESPIRATORY-DISTRESS-SYNDROME | CELL & TISSUE ENGINEERING | CELL BIOLOGY | INTRATRACHEAL INSTILLATION | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | EPITHELIAL FLUID TRANSPORT | ANTIGEN-PRESENTING CELL | ANGIOPOIETIN-1 GENE-THERAPY | HEMATOLOGY | PULMONARY-EDEMA FLUID | Acute Lung Injury - physiopathology | Lung - pathology | Pneumonia, Bacterial - microbiology | Capillary Permeability | Paracrine Communication | Acute Lung Injury - therapy | Immunomodulation | Humans | Pneumonia, Bacterial - etiology | Mesenchymal Stromal Cells - metabolism | Clinical Trials as Topic | Lung - physiopathology | Acute Lung Injury - pathology | Mesenchymal Stem Cell Transplantation - adverse effects | Pneumonia, Bacterial - prevention & control | Mesenchymal Stromal Cells - immunology | Intercellular Signaling Peptides and Proteins - metabolism | Regeneration | Animals | Lung - metabolism | Disease Models, Animal
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