Suchergebnisse - "Endothelial Cells/immunology"

Immunoregulatory Endothelial Cells Interact With T Cells After Myocardial Infarction

Autoren: Lukas S. Tombor Till Lautenschläger Simone F. Glaser et al.

Quelle: Circulation Research. 137:866-879

Schlagwörter: Male, 210002 Nanobiotechnologie, Cells, Knockout, infarction, Cell Communication, ischemia, Inbred C57BL, 301207 Pharmazeutische Chemie, Mice, 210002 Nanobiotechnology, Animals, 304004 Gentherapie, T-lymphocytes, 304004 Gene therapy, Cultured, Animal, Core Binding Factor Alpha 2 Subunit/metabolism, Cytokines/metabolism, Endothelial Cells/immunology, T-Lymphocytes/immunology, endothelial cells, inflammation, Disease Models, Myocardial Infarction/immunology, 301207 Pharmaceutical chemistry

Cytotoxic Responses Mediated by NK Cells and Cytotoxic T Lymphocytes in Xenotransplantation

Autoren: Galdina, Viktoriia Puga Yung, Gisella Seebach, Jorg Dieter

Quelle: Transpl Int
Transplant International, Vol 38 (2025)

Schlagwörter: Graft Rejection, Cytotoxicity, Immunologic, Graft Rejection / prevention & control, Swine, Transplantation, Heterologous, Graft Survival, porcine endothelium, Specialties of internal medicine, Endothelial Cells, Graft Rejection / immunology, NK cells, CD8+ T cells, Graft Survival / immunology, Health Archive, xenograft rejection, T-Lymphocytes, Cytotoxic / immunology, Killer Cells, Natural, Endothelial Cells / immunology, RC581-951, cytotoxicity, Animals, Humans, Killer Cells, Natural / immunology, T-Lymphocytes, Cytotoxic

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/40012743
https://doaj.org/article/c2ec6559f83d4ba7b8090c1aa52434e0
https://archive-ouverte.unige.ch/unige:183682
https://doi.org/10.3389/ti.2025.13867

Lymphatic-derived oxysterols promote anti-tumor immunity and response to immunotherapy in melanoma

Autoren: Mengzhu Sun Laure Garnier Romane Chevalier et al.

Weitere Verfasser: Mengzhu Sun Laure Garnier Romane Chevalier et al.

Quelle: Nat Commun
Nature Communications, Vol 16, Iss 1, Pp 1-22 (2025)
Nature Communications, Vol. 16, no.1 (2025)
Nature communications, vol. 16, no. 1, pp. 1217

Schlagwörter: EXPRESSION, Male, Science, Animals, Humans, Immunotherapy/methods, Melanoma/immunology, Melanoma/therapy, Mice, Hydroxycholesterols/metabolism, Endothelial Cells/immunology, Endothelial Cells/metabolism, Mice, Inbred C57BL, Oxysterols/metabolism, Cell Line, Tumor, Lymphangiogenesis/drug effects, Lymphatic Vessels/immunology, Lymphatic Vessels/pathology, Macrophages/immunology, Macrophages/metabolism, Female, Melanoma, Experimental/immunology, Melanoma, Experimental/therapy, Steroid Hydroxylases, Melanoma, Experimental, CELL-MIGRATION, Article, ACTIVATION, TUMOR, REVEALS, MACROPHAGES, Lymphangiogenesis, Melanoma, Lymphatic Vessels, Science & Technology, Macrophages, Endothelial Cells, Oxysterols, Hydroxycholesterols, Multidisciplinary Sciences, RECEPTORS, MONOCYTES, Science & Technology - Other Topics, PPAR-GAMMA, Immunotherapy, LYMPHANGIOGENESIS

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/39890772
https://doaj.org/article/0af122abda854646bb7ed8b7aa8c081f
https://hdl.handle.net/2078.1/303168
https://serval.unil.ch/notice/serval:BIB_BADF9D7710DC
https://serval.unil.ch/resource/serval:BIB_BADF9D7710DC.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_BADF9D7710DC6

Transcriptional signatures of endothelial cells shape immune responses in cardiopulmonary health and disease

Autoren: Fließer, Elisabeth Jandl, Katharina Chen, Shiau-Haln et al.

Quelle: Fließer, E, Jandl, K, Chen, S-H, Wang, M-T, Schupp, J C, Kuebler, W M, Baker, A H & Kwapiszewska, G 2025, 'Transcriptional signatures of endothelial cells shape immune responses in cardiopulmonary health and disease', JCI INSIGHT, vol. 10, no. 10, e191059. https://doi.org/10.1172/jci.insight.191059

Schlagwörter: Humans, Endothelial Cells/immunology metabolism, Lung/immunology blood supply, Lung Diseases/immunology genetics, Animals, Transcriptome, Immunomodulation/genetics, Single-Cell Analysis

Relation: info:eu-repo/semantics/altIdentifier/pissn/2379-3708

Verfügbarkeit: https://cris.maastrichtuniversity.nl/en/publications/83e1ab41-8c98-4318-bb15-a6e3cb03f9c0
https://doi.org/10.1172/jci.insight.191059
https://www.scopus.com/pages/publications/105006425206

Perivascular B cells link intestinal angiogenesis to immunity and to the gut-brain axis during neuroinflammation.

Autoren: Peter, B. Rebeaud, J. Vigne, S. et al.

Quelle: Journal of autoimmunity, vol. 148, pp. 103292

Schlagwörter: Animals, Mice, Encephalomyelitis, Autoimmune, Experimental/immunology, Experimental/pathology, Experimental/metabolism, B-Lymphocytes/immunology, B-Lymphocytes/metabolism, Brain-Gut Axis/immunology, Neovascularization, Pathologic/immunology, Endothelial Cells/immunology, Endothelial Cells/metabolism, Neuroinflammatory Diseases/immunology, Neuroinflammatory Diseases/etiology, Neuroinflammatory Diseases/pathology, Neuroinflammatory Diseases/metabolism, Disease Models, Animal, Intestinal Mucosa/immunology, Intestinal Mucosa/pathology, Intestinal Mucosa/metabolism, Intestines/immunology, Intestines/blood supply, Intestines/pathology, Inbred C57BL, Cell Proliferation, Female, Multiple Sclerosis/immunology

Dateibeschreibung: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/39067313; info:eu-repo/semantics/altIdentifier/eissn/1095-9157; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_4306784A31225; https://serval.unil.ch/notice/serval:BIB_4306784A3122; https://serval.unil.ch/resource/serval:BIB_4306784A3122.P001/REF.pdf

Verfügbarkeit: https://serval.unil.ch/notice/serval:BIB_4306784A3122
https://doi.org/10.1016/j.jaut.2024.103292
https://serval.unil.ch/resource/serval:BIB_4306784A3122.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4306784A31225

Circadian tumor infiltration and function of CD8+ T cells dictate immunotherapy efficacy.

Autoren: Wang, C. Zeng, Q. Gül, Z.M. et al.

Quelle: Cell, vol. 187, no. 11, pp. 2690-2702.e17

Schlagwörter: Animals, Humans, Mice, CD8-Positive T-Lymphocytes/immunology, Cell Line, Tumor, Circadian Clocks, Circadian Rhythm, Endothelial Cells/immunology, Immune Checkpoint Inhibitors/therapeutic use, Immune Checkpoint Inhibitors/pharmacology, Immunotherapy/methods, Lymphocytes, Tumor-Infiltrating/immunology, Melanoma/immunology, Melanoma/therapy, Melanoma/pathology, Inbred C57BL, Tumor Microenvironment/immunology, BMAL1, CAR T therapy, PD-1, chronotherapy, circadian, immune checkpoint blockade, immunology, melanoma, tumor-infiltrating leukocyte

Dateibeschreibung: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/38723627; info:eu-repo/semantics/altIdentifier/eissn/1097-4172; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_BEDDA80F90135; https://serval.unil.ch/notice/serval:BIB_BEDDA80F9013; https://serval.unil.ch/resource/serval:BIB_BEDDA80F9013.P001/REF.pdf

Verfügbarkeit: https://serval.unil.ch/notice/serval:BIB_BEDDA80F9013
https://doi.org/10.1016/j.cell.2024.04.015
https://serval.unil.ch/resource/serval:BIB_BEDDA80F9013.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_BEDDA80F90135

Myeloid SOCS3 Deficiency Regulates Angiogenesis via Enhanced Apoptotic Endothelial Cell Engulfment

Autoren: Korovina, Irina Neuwirth, Ales Sprott, David et al.

Quelle: Journal of Innate Immunity. 12:248-256

Schlagwörter: 0301 basic medicine, Mice, 0303 health sciences, 03 medical and health sciences, Phagocytosis, Suppressor of Cytokine Signaling 3 Protein, Apoptosis/immunology [MeSH], Neovascularization, Physiologic/genetics [MeSH], Suppressor of Cytokine Signaling 3 Protein/immunology [MeSH], Suppressor of Cytokine Signaling 3 Protein/deficiency [MeSH], Myeloid Cells/immunology [MeSH], Animals [MeSH], Mice, Transgenic [MeSH], Mice [MeSH], Suppressor of cytokine signaling 3, Phagocytosis [MeSH], Growth arrest-specific 6, Mer, Apoptosis/genetics [MeSH], Endothelial Cells/immunology [MeSH], Angiogenesis, Research Article, Neovascularization, Physiologic/immunology [MeSH], Animals, Endothelial Cells, Neovascularization, Physiologic, Apoptosis, Mice, Transgenic, Myeloid Cells

Zugangs-URL: https://www.karger.com/Article/Pdf/502645
https://pubmed.ncbi.nlm.nih.gov/31574508
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265721
https://europepmc.org/article/MED/31574508
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265721
https://pubmed.ncbi.nlm.nih.gov/31574508/
https://repository.publisso.de/resource/frl:6478875

Complement Activation and Thrombin Generation by MBL Bound to β2-Glycoprotein I

Autoren: Paolo Durigutto Paolo Macor Nicola Pozzi et al.

Weitere Verfasser: Paolo Durigutto Paolo Macor Nicola Pozzi et al.

Quelle: The Journal of Immunology. 205:1385-1392

Schlagwörter: 0301 basic medicine, Calcium/metabolism, Human Umbilical Vein Endothelial Cell, Mannose-Binding Lectin, Endothelium/immunology, Cell Line, 03 medical and health sciences, Human Umbilical Vein Endothelial Cells, Thrombosis/immunology, Humans, Endothelium, Complement Activation, Antiphospholipid Syndrome, Calcium, Endothelial Cells, Protein Binding, Thrombin, Thrombosis, Tumor Necrosis Factor-alpha, beta 2-Glycoprotein I, Endothelial Cell, 0303 health sciences, Protein Binding/immunology, Complement Activation/immunology, Antiphospholipid Syndrome/immunology, beta 2-Glycoprotein I/immunology, Endothelial Cells/immunology, Tumor Necrosis Factor-alpha/immunology, Thrombin/immunology, Thrombosi, Mannose-Binding Lectin/immunology, Human

Dateibeschreibung: application/pdf

Zugangs-URL: https://www.jimmunol.org/content/jimmunol/205/5/1385.full.pdf
https://pubmed.ncbi.nlm.nih.gov/32759297
https://www.jimmunol.org/content/205/5/1385
http://hdl.handle.net/11368/2992293
https://europepmc.org/articles/PMC7489996/
https://moh-it.pure.elsevier.com/en/publications/complement-activation-and-thrombin-generation-by-mbl-bound-to-b2--2
https://pubmed.ncbi.nlm.nih.gov/32759297/
https://www.ncbi.nlm.nih.gov/pubmed/32759297
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489996
https://www.jimmunol.org/content/205/5/1385
https://hdl.handle.net/11368/2992293
https://doi.org/10.4049/jimmunol.2000570

Fibroblast‐derived IL‐33 is dispensable for lymph node homeostasis but critical for CD8 T‐cell responses to acute and chronic viral infection

Autoren: Patricia Aparicio‐Domingo Hélène Cannelle Matthew B. Buechler et al.

Quelle: European journal of immunology, vol. 51, no. 1, pp. 76-90

Schlagwörter: Male, Mice, Knockout, EMC OR-01, Models, Immunological, Endothelial Cells, Mice, Transgenic, Adaptive Immunity, CD8-Positive T-Lymphocytes, Fibroblasts, Lymphocytic Choriomeningitis, Interleukin-33, Immunity, Innate, 3. Good health, Mice, Inbred C57BL, Mice, Acute Disease, Chronic Disease, Animals, CD8-Positive T-Lymphocytes/immunology, Endothelial Cells/immunology, Fibroblasts/immunology, Homeostasis, Humans, Interleukin-33/deficiency, Interleukin-33/genetics, Interleukin-33/metabolism, Lymph Nodes/immunology, Lymphocytic Choriomeningitis/immunology, Lymphocytic choriomeningitis virus/immunology, FRC, LCMV, alarmin, fibroblastic reticular cells, Lymphocytic choriomeningitis virus, Lymph Nodes

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/32700362
https://repub.eur.nl/pub/129390
https://www.ncbi.nlm.nih.gov/pubmed/32700362
https://onlinelibrary.wiley.com/doi/abs/10.1002/eji.201948413
https://pubmed.ncbi.nlm.nih.gov/32700362/
https://serval.unil.ch/notice/serval:BIB_74E3A21E1736
https://serval.unil.ch/notice/serval:BIB_74E3A21E1736
https://serval.unil.ch/resource/serval:BIB_74E3A21E1736.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_74E3A21E17369

Translational implications of endothelial cell dysfunction in association with chronic allograft rejection

Autoren: Bruneau, S. Wedel, J. Fakhouri, F. et al.

Schlagwörter: Allografts, Animals, Biomarkers/metabolism, Cellular Microenvironment, Chronic Disease, Endothelial Cells/immunology/*metabolism, Gene Expression Regulation, Graft Rejection/*etiology/genetics/immunology/metabolism/physiopathology, Graft Survival, Humans, Kidney/*blood supply, Kidney Transplantation/*adverse effects, MicroRNAs/genetics/metabolism, Microvessels/immunology/*metabolism/physiopathology, Risk Factors, Time Factors, Translational Research, Biomedical, Treatment Outcome, Biomarkers, Endothelial cells, Graft rejection, Preventative therapeutics, Vascular endothelial growth factor, mTOR-mediated signaling, miRNA

Relation: Pediatric Nephrology; https://iris.unil.ch/handle/iris/46634; serval:BIB_33C6FA51CAB9

Verfügbarkeit: https://iris.unil.ch/handle/iris/46634
https://doi.org/10.1007/s00467-015-3094-6

Cannabidiol attenuates high glucose-induced endothelial cell inflammatory response and barrier disruption.

Autoren: Rajesh, M. Mukhopadhyay, P. Bátkai, S. et al.

Schlagwörter: Cannabidiol/administration & dosage, Cell Adhesion/drug effects, Cells, Cultured, Cytokines/immunology, Dose-Response Relationship, Drug, Endothelial Cells/drug effects, Endothelial Cells/immunology, Glucose/administration & dosage, Humans, Inflammation Mediators/immunology, Monocytes/drug effects, Monocytes/immunology

Dateibeschreibung: application/pdf

Relation: American Journal of Physiology - Heart and Circulatory Physiology; https://iris.unil.ch/handle/iris/208735; serval:BIB_A6D8869DE0A7; 000247968800074

Verfügbarkeit: https://iris.unil.ch/handle/iris/208735
https://doi.org/10.1152/ajpheart.00236.2007

Contribution of (sub)domains of Staphylococcus aureus fibronectin-binding protein to the proinflammatory and procoagulant response of human vascular endothelial cells.

Autoren: Heying, R. van de Gevel, J. Que, Y.A. et al.

Schlagwörter: Adhesins, Bacterial/genetics, Bacterial/immunology, Cells, Cultured, Endothelial Cells/immunology, Endothelial Cells/metabolism, Fibronectins/metabolism, Humans, Lactococcus lactis/genetics, Mutant Proteins/genetics, Mutant Proteins/immunology, Staphylococcal Infections/genetics, Staphylococcal Infections/immunology, Staphylococcus aureus/genetics, Staphylococcus aureus/immunology, Thromboplastin/metabolism

Relation: Thrombosis and Haemostasis; https://iris.unil.ch/handle/iris/166877; serval:BIB_AE718F07FC46; 000264382400015

Verfügbarkeit: https://iris.unil.ch/handle/iris/166877
https://doi.org/10.1160/TH08-06-0395

Platelet hyaluronidase-2 regulates the early stages of inflammatory disease in colitis

Autoren: Aaron C. Petrey Dana R. Obery Sean P. Kessler et al.

Quelle: Petrey, A C, Obery, D R, Kessler, S P, Zawerton, A, Flamion, B & de la Motte, C A 2019, 'Platelet hyaluronidase-2 regulates the early stages of inflammatory disease in colitis', Blood, vol. 134, no. 9, pp. 765-775. https://doi.org/10.1182/blood.2018893594

Schlagwörter: Blood Platelets, 0301 basic medicine, Inflammatory Bowel Diseases/immunology, Cells, Knockout, Hyaluronoglucosaminidase, GPI-Linked Proteins, Mice, 03 medical and health sciences, GPI-Linked Proteins/immunology, Animals, Humans, Colitis/immunology, Hyaluronic Acid/immunology, Hyaluronic Acid, Blood Platelets/immunology, Cells, Cultured, Inflammation, Mice, Knockout, 0303 health sciences, Cultured, Hyaluronoglucosaminidase/immunology, Endothelial Cells/immunology, Endothelial Cells, Inflammation/immunology, Colitis, Inflammatory Bowel Diseases, 3. Good health

Dateibeschreibung: application/pdf

Zugangs-URL: https://ashpublications.org/blood/article-pdf/134/9/765/1554331/blood893594.pdf
https://pubmed.ncbi.nlm.nih.gov/31262781
https://researchportal.unamur.be/en/publications/95a2f13d-64a5-4058-9d3f-ffcc111f9575
https://doi.org/10.1182/blood.2018893594
https://pubmed.ncbi.nlm.nih.gov/31262781/
https://ashpublications.org/blood/article/134/9/765/260778/Platelet-hyaluronidase-2-regulates-the-early
https://europepmc.org/article/MED/31262781
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716076
https://www.ncbi.nlm.nih.gov/pubmed/31262781
https://www.sciencedirect.com/science/article/pii/S000649712072327X
https://pure.unamur.be/ws/files/54064036/blood893594.pdf

Antibody-Mediated Neutralization of uPA Proteolytic Function Reduces Disease Progression in Mouse Arthritis Models

Autoren: Josephine B Hebsgaard Kasper Almholt Anneline Nansen et al.

Quelle: The Journal of Immunology. 200:957-965

Schlagwörter: Male, 0301 basic medicine, Neutrophils, Macrophages/immunology, Delayed/immunology, Inbred C57BL, Antibodies, Etanercept, Receptors, Urokinase Plasminogen Activator, Arthritis, Rheumatoid, Mice, 03 medical and health sciences, 0302 clinical medicine, Receptors, Hypersensitivity, Inbred DBA, Animals, Humans, Experimental/pathology, Hypersensitivity, Delayed, Synovial Membrane/immunology, 2. Zero hunger, 0303 health sciences, Urokinase-Type Plasminogen Activator/antagonists & inhibitors, Animal, Tumor Necrosis Factor-alpha/antagonists & inhibitors, Tumor Necrosis Factor-alpha, Arthritis, Macrophages, Neutrophils/immunology, Synovial Membrane, Endothelial Cells/immunology, Etanercept/pharmacology, Antibodies, Monoclonal, Endothelial Cells, Arthritis, Experimental, 3. Good health, Mice, Inbred C57BL, Disease Models, Animal, Urokinase Plasminogen Activator/metabolism, Mice, Inbred DBA, Disease Models, Disease Progression, Female, Monoclonal/immunology, Rheumatoid/pathology

Zugangs-URL: https://www.jimmunol.org/content/jimmunol/200/3/957.full.pdf
https://pubmed.ncbi.nlm.nih.gov/29282305
https://www.ncbi.nlm.nih.gov/pubmed/29282305
https://pubmed.ncbi.nlm.nih.gov/29282305/
https://europepmc.org/article/MED/29282305

Acid Sphingomyelinase–Derived Ceramide Regulates ICAM-1 Function during T Cell Transmigration across Brain Endothelial Cells

Autoren: Melissa A Lopes Pinheiro Jeffrey Kroon Mark Hoogenboezem et al.

Quelle: Lopes Pinheiro, M A, Kroon, J, Hoogenboezem, M, Geerts, D, van Het Hof, B, van der Pol, S M A, van Buul, J D & de Vries, H E 2016, 'Acid Sphingomyelinase-Derived Ceramide Regulates ICAM-1 Function during T Cell Transmigration across Brain Endothelial Cells', Journal of Immunology, vol. 196, no. 1, pp. 72-79. https://doi.org/10.4049/jimmunol.1500702

Schlagwörter: Adult, Male, 0301 basic medicine, Multiple Sclerosis, Cell Adhesion/genetics, Filamins, T-Lymphocytes, Intercellular Adhesion Molecule-1/biosynthesis, Ceramides, Cell Line, 03 medical and health sciences, Ceramides/metabolism, 80 and over, Cell Adhesion, Humans, Sphingomyelin Phosphodiesterase/genetics, Multiple Sclerosis/immunology, Phosphorylation, Filamins/metabolism, Aged, Aged, 80 and over, 0303 health sciences, Cytoskeletal Proteins/metabolism, Transendothelial and Transepithelial Migration, Endothelial Cells/immunology, Brain, Endothelial Cells, T-Lymphocytes/immunology, EMC MM-02-54-03, Middle Aged, Transendothelial and Transepithelial Migration/immunology, Intercellular Adhesion Molecule-1, Cytoskeletal Proteins, Sphingomyelin Phosphodiesterase, Brain/cytology, Phosphorylation/genetics, Female

Zugangs-URL: https://www.jimmunol.org/content/jimmunol/196/1/72.full.pdf
https://pubmed.ncbi.nlm.nih.gov/26597010
https://europepmc.org/article/MED/26597010
https://pubmed.ncbi.nlm.nih.gov/26597010/
https://www.ncbi.nlm.nih.gov/pubmed/26597010
https://research.vumc.nl/en/publications/acid-sphingomyelinase-derived-ceramide-regulates-icam-1-function-
http://www.jimmunol.org/content/jimmunol/196/1/72.full.pdf
https://www.narcis.nl/publication/RecordID/oai%3Apure.amc.nl%3Apublications%2F76230c07-4226-4efa-8ec8-688174488561
https://research.vumc.nl/en/publications/fc7bdd95-cd9e-4af2-a14f-f0420c8273d5

Phenotypic Variation in Aicardi–Goutières Syndrome Explained by Cell-Specific IFN-Stimulated Gene Response and Cytokine Release

Autoren: Machiel H. Jansen Lidia De Filippis Angelo L. Vescovi et al.

Weitere Verfasser: Machiel H. Jansen Lidia De Filippis Angelo L. Vescovi et al.

Quelle: Cuadrado, E, Michailidou, I, van Bodegraven, E J, Jansen, M H, Sluijs, J A, Geerts, D, Couraud, P-O, De Filippis, L, Vescovi, A L, Kuijpers, T W & Hol, E M 2015, 'Phenotypic variation in Aicardi-Goutières syndrome explained by cell-specific IFN-stimulated gene response and cytokine release', Journal of Immunology, vol. 194, no. 8, pp. 3623-33. https://doi.org/10.4049/jimmunol.1401334

Schlagwörter: 0301 basic medicine, Astrocytes/immunology, Exodeoxyribonucleases/genetics, Autoimmune Diseases of the Nervous System/genetics, Adenosine Deaminase, Interferon-alpha/genetics, Immunology, Ribonuclease H, Nervous System Malformations, Monomeric GTP-Binding Proteins/genetics, SAM Domain and HD Domain-Containing Protein 1, 03 medical and health sciences, Autoimmune Diseases of the Nervous System, Neural Stem Cells, Phosphoproteins/genetics, Taverne, Neural Stem Cells/immunology, Journal Article, Humans, Gene Silencing, Monomeric GTP-Binding Proteins, 0303 health sciences, Cytokines/genetics, Research Support, Non-U.S. Gov't, Endothelial Cells/immunology, Endothelial Cells, Interferon-alpha, RNA-Binding Proteins, Ribonuclease H/genetics, EMC MM-02-54-03, Phosphoproteins, RNA-Binding Proteins/genetics, 3. Good health, Exodeoxyribonucleases, HEK293 Cells, Astrocytes, Cytokines, Mutation, Adenosine Deaminase/genetics, Nervous System Malformations/genetics

Dateibeschreibung: application/pdf

Zugangs-URL: https://www.jimmunol.org/content/jimmunol/194/8/3623.full.pdf
https://pubmed.ncbi.nlm.nih.gov/25769924
https://europepmc.org/abstract/MED/25769924
http://www.jimmunol.org/lookup/doi/10.4049/jimmunol.1401334
https://repub.eur.nl/pub/84282
https://www.ncbi.nlm.nih.gov/pubmed/25769924
https://pure.knaw.nl/ws/files/2109943/Cuadrado2015JImmunol.pdf
https://moh-it.pure.elsevier.com/en/publications/phenotypic-variation-in-aicardi-gouti%C3%A8res-syndrome-explained-by-c
https://research.vumc.nl/en/publications/efa4e71f-d194-4310-aa85-d083d3aa5da9
https://dspace.library.uu.nl/handle/1874/331333

Serum Reactivity Against Herpes Simplex Virus Type 1 UL48 Protein in Behçet’s Disease Patients and a Behçet’s Disease-like Mouse Model

Autoren: Zhenlong Zheng Dongsik Bang Keun Jae Ahn et al.

Weitere Verfasser: Zhenlong Zheng Dongsik Bang Keun Jae Ahn et al.

Quelle: Acta Dermato Venereologica. 95:952-958

Schlagwörter: Adult, Male, 0301 basic medicine, Microvessels/immunology, Herpesvirus 1, Human, Cross Reactions, Behçet's disease-like mouse model, Young Adult, Behçet's disease, Mice, Viral Proteins, 03 medical and health sciences, proteomics, Animals, Humans, UL48, Recombinant Proteins/immunology, Human/immunology, Mice, Inbred ICR, 0303 health sciences, Behcet Syndrome/blood, Immunoglobulin G/blood, Animal, Herpesvirus 1, Behcet Syndrome, HSC70 Heat-Shock Proteins, Endothelial Cells/immunology, Endothelial Cells, Middle Aged, herpes simplex virus, Inbred ICR, heat shock cognate 71 kDa protein, Recombinant Proteins, Immunoglobulin A, 3. Good health, Immunoglobulin A/blood, Disease Models, Animal, Case-Control Studies, Immunoglobulin G, Disease Models, Microvessels, Female, HSC70 Heat-Shock Proteins/immunology, Viral Proteins/immunology

Dateibeschreibung: 952~958

Zugangs-URL: https://www.medicaljournals.se/acta/download/10.2340/00015555-2127/
https://pubmed.ncbi.nlm.nih.gov/25916670
https://pubmed.ncbi.nlm.nih.gov/25916670/
https://www.ncbi.nlm.nih.gov/pubmed/25916670
https://www.medicaljournals.se/acta/content/?doi=10.2340/00015555-2127

Liver X Receptor Alpha Is Important in Maintaining Blood-Brain Barrier Function

Autoren: Elien Wouters Nienke M. de Wit Jasmine Vanmol et al.

Quelle: Front Immunol
Frontiers in Immunology, Vol 10 (2019)
Wouters, E, de Wit, N M, Vanmol, J, van der Pol, S M A, van Het Hof, B, Sommer, D, Loix, M, Geerts, D, Gustafsson, J A, Steffensen, K R, Vanmierlo, T, Bogie, J F J, Hendriks, J J A & de Vries, H E 2019, 'Liver X Receptor Alpha Is Important in Maintaining Blood-Brain Barrier Function', Frontiers in Immunology, vol. 10, pp. 1811. https://doi.org/10.3389/fimmu.2019.01811

Schlagwörter: EXPRESSION, DISRUPTION, 0301 basic medicine, Encephalomyelitis, Autoimmune, Experimental, endothelium, Knockout, Immunology, ISCHEMIC BRAIN, BETA, Vascular Cell Adhesion Molecule-1, Vascular Cell Adhesion Molecule-1/genetics, neuroinflammation, Cell Line, ACTIVATION, liver X receptors, Mice, 03 medical and health sciences, Liver X Receptors/genetics, DEFICIENT, LIPID-METABOLISM, Animals, Humans, Experimental/genetics, Encephalomyelitis, Liver X Receptors, blood-brain barrier, permeability, Mice, Knockout, 0303 health sciences, LXR-ALPHA, Blood-Brain Barrier/immunology, Endothelial Cells/immunology, Endothelial Cells, RC581-607, ENDOTHELIAL-CELLS, 3. Good health, MONOCYTES, Blood-Brain Barrier, Gene Knockdown Techniques, Immunologic diseases. Allergy, Autoimmune

Dateibeschreibung: application/pdf

Zugangs-URL: https://www.frontiersin.org/articles/10.3389/fimmu.2019.01811/pdf
https://pubmed.ncbi.nlm.nih.gov/31417573
https://doaj.org/article/56fc8933ec1142a69ee5c39bf8b09233
https://research.vumc.nl/en/publications/liver-x-receptor-alpha-is-important-in-maintaining-blood-brain-ba
https://scholars.houstonmethodist.org/en/publications/liver-x-receptor-alpha-is-important-in-maintaining-blood-brain-ba
https://www.narcis.nl/publication/RecordID/oai%3Apure.atira.dk%3Apublications%2F34833f5a-f811-4a86-a65d-56a348ce7f6c
https://figshare.com/collections/Liver_X_Receptor_Alpha_Is_Important_in_Maintaining_Blood-Brain_Barrier_Function/4602224
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685401
https://europepmc.org/abstract/MED/31417573
https://research.vumc.nl/en/publications/34833f5a-f811-4a86-a65d-56a348ce7f6c
https://pure.amsterdamumc.nl/en/publications/52f69205-e68c-4154-8289-ec2a89c7020b
https://doi.org/10.3389/fimmu.2019.01811
http://hdl.handle.net/1942/29080

The Potential of Endothelial Colony-Forming Cells to Improve Early Graft Loss after Intraportal Islet Transplantation

Autoren: Kyong Soo Park Hakmo Lee Hye Seung Jung et al.

Weitere Verfasser: Kyong Soo Park Hakmo Lee Hye Seung Jung et al.

Quelle: Cell Transplantation, Vol 23 (2014)

Schlagwörter: Blood Glucose, Graft Rejection, Swine, Nude, Islets of Langerhans Transplantation, Tumor Necrosis Factor-alpha/analysis, Endothelial progenitor cell, Islets of Langerhans Transplantation/methods, Mice, 0302 clinical medicine, HMGB1 Protein, High-mobility group box 1 (HMGB1), Cells, Cultured, Heterologous, Cultured, Stem Cells, Inflammation/immunology, Stem Cells/immunology, 3. Good health, Early graft loss, Medicine, Graft Rejection/prevention & control, Islets of Langerhans Transplantation/immunology, Cells, Transplantation, Heterologous, Mice, Nude, Islet transplantation (ITx), Diabetes Mellitus, Experimental, Endothelial colony-forming cells (ECFCs), Islets of Langerhans, 03 medical and health sciences, Diabetes Mellitus, Islets of Langerhans/immunology, Animals, Humans, Inflammation, Transplantation, Instant blood-mediated inflammatory reaction (IBMIR), Tumor Necrosis Factor-alpha, Endothelial Cells/cytology, Endothelial Cells/immunology, Endothelial Cells, Blood Glucose/analysis, Graft Rejection/immunology, Experimental/surgery, Islets of Langerhans/cytology, Coculture Techniques, HMGB1 Protein/analysis, Stem Cells/cytology, Coculture Techniques/methods

Dateibeschreibung: 273~283

Zugangs-URL: http://journals.sagepub.com/doi/pdf/10.3727/096368912X661364
https://pubmed.ncbi.nlm.nih.gov/23294520
https://doaj.org/article/71b493198797484080cf333ba6bd0ff0
https://europepmc.org/article/MED/23294520
https://pubmed.ncbi.nlm.nih.gov/23294520/
https://www.ncbi.nlm.nih.gov/pubmed/23294520
https://journals.sagepub.com/doi/10.3727/096368912X661364
https://snucm.elsevierpure.com/en/publications/the-potential-of-endothelial-colony-forming-cells-to-improve-earl
http://journals.sagepub.com/doi/10.3727/096368912X661364

Saikosaponin C inhibits lipopolysaccharide-induced apoptosis by suppressing caspase-3 activation and subsequent degradation of focal adhesion kinase in human umbilical vein endothelial cells

Autoren: Byeong Mo Kim Jihoon Chang Tae Ho Lee et al.

Weitere Verfasser: Byeong Mo Kim Jihoon Chang Tae Ho Lee et al.

Quelle: Biochemical and Biophysical Research Communications. 445:615-621

Schlagwörter: Focal adhesion kinase (FAK), Lipopolysaccharides, 0301 basic medicine, Non-Steroidal/chemistry, Lipopolysaccharides/immunology, Anti-Inflammatory Agents, Human Umbilical Vein Endothelial Cells/cytology, Lipopolysaccharide (LPS), Apoptosis, Non-Steroidal/pharmacology, 03 medical and health sciences, Human Umbilical Vein Endothelial Cells, Humans, Endothelial cell apoptosis, Bupleurum/chemistry, Oleanolic Acid, Focal Adhesion Protein-Tyrosine Kinases/immunology, 0303 health sciences, Human Umbilical Vein Endothelial Cells/drug effects, Oleanolic Acid/pharmacology, Caspase 3/immunology, Caspase 3, Oleanolic Acid/chemistry, Apoptosis/drug effects, Anti-Inflammatory Agents, Non-Steroidal, Saponins, Bupleurum, 3. Good health, Caspase-3, Oleanolic Acid/analogs & derivatives, Saikosaponin C (SSc), Focal Adhesion Protein-Tyrosine Kinases, Human umbilical vein endothelial cells (HUVECs), Human Umbilical Vein Endothelial Cells/immunology, Saponins/pharmacology, Saponins/chemistry

Dateibeschreibung: 615~621

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/24565837
https://www.sciencedirect.com/science/article/pii/S0006291X14003088
https://pubag.nal.usda.gov/catalog/5329713
https://ir.ymlib.yonsei.ac.kr/handle/22282913/138761