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    Wyświetlanie 1-20 z 20
    Tytuł:
    Comparison of permeable cell culture inserts for use in culture of a human in vitro air-liquid interface model system.
    Autorzy:
    Brocke SA; Curriculum in Toxicology and Environmental Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
    Speen AM; Center for Environmental Medicine, Asthma, and Lung Biology, University of North Carolina, Chapel Hill, North Carolina, USA.
    Masood S; Curriculum in Toxicology and Environmental Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
    Worden CP; Department of Otolaryngology, Head and Neck Surgery, University of North Carolina, Chapel Hill, North Carolina, USA.
    Jaspers I; Curriculum in Toxicology and Environmental Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.; Center for Environmental Medicine, Asthma, and Lung Biology, University of North Carolina, Chapel Hill, North Carolina, USA.
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    Źródło:
    Physiological reports [Physiol Rep] 2024 Feb; Vol. 12 (3), pp. e15921.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Cell Culture Techniques*/methods
    Epithelial Cells*/metabolism
    Humans ; Male ; Respiratory System ; Cells, Cultured ; Cell Differentiation
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Simple graphical approach to investigate differences in transepithelial paracellular leak pathway permeability.
    Autorzy:
    Monaco A; Department of Biomedical Sciences, NYIT College of Osteopathic Medicine, Old Westbury, New York, USA.
    Axis J; Department of Biomedical Sciences, NYIT College of Osteopathic Medicine, Old Westbury, New York, USA.
    Amsler K; Department of Biomedical Sciences, NYIT College of Osteopathic Medicine, Old Westbury, New York, USA.
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    Źródło:
    Physiological reports [Physiol Rep] 2022 Mar; Vol. 10 (5), pp. e15202.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Epithelial Cells*/metabolism
    Tight Junctions*/metabolism
    Permeability
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Expression of SARS-CoV-2 entry factors, electrolyte, and mineral transporters in different mouse intestinal epithelial cell types.
    Autorzy:
    Pearce SC; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
    Suntornsaratoon P; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.; Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
    Kishida K; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
    Al-Jawadi A; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
    Guardia J; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
    Nadler I; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
    Flores J; Department of Biological Sciences, Life Science Center, Rutgers University, Newark, New Jersey, USA.
    Shiarella R; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
    Auvinen M; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
    Yu S; Department of Biological Sciences, Life Science Center, Rutgers University, Newark, New Jersey, USA.
    Gao N; Department of Biological Sciences, Life Science Center, Rutgers University, Newark, New Jersey, USA.
    Ferraris RP; Department of Pharmacology, Physiology and Neurosciences, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
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    Źródło:
    Physiological reports [Physiol Rep] 2021 Nov; Vol. 9 (21), pp. e15061.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
    MeSH Terms:
    COVID-19/*virology
    Electrolytes/*metabolism
    Epithelial Cells/*metabolism
    Intestines/*physiology
    Membrane Transport Proteins/*metabolism
    Minerals/*metabolism
    SARS-CoV-2/*metabolism
    Angiotensin-Converting Enzyme 2/metabolism ; Animals ; COVID-19/metabolism ; COVID-19/pathology ; COVID-19/transmission ; Epithelial Cells/cytology ; Epithelial Cells/virology ; Immunohistochemistry ; Intestines/cytology ; Intestines/virology ; Male ; Membrane Proteins/metabolism ; Mice ; SARS-CoV-2/isolation & purification ; Serine Endopeptidases/metabolism
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    β3 adrenergic receptor as potential therapeutic target in ADPKD.
    Autorzy:
    Schena G; Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut, USA.
    Carmosino M; Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut, USA.; Department of Sciences, University of Basilicata, Potenza, Italy.
    Chiurlia S; Schena Foundation, Valenzano, Italy.
    Onuchic L; Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut, USA.
    Mastropasqua M; Department of Emergency and Organ Transplantation, Section of Pathological Anatomy, University of Bari, Bari, Italy.
    Maiorano E; Department of Emergency and Organ Transplantation, Section of Pathological Anatomy, University of Bari, Bari, Italy.
    Schena FP; Schena Foundation, Valenzano, Italy.; Department of Emergency and Organ Transplantation, Section of Nephrology, University of Bari, Bari, Italy.
    Caplan MJ; Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut, USA.
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    Źródło:
    Physiological reports [Physiol Rep] 2021 Oct; Vol. 9 (20), pp. e15058.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
    MeSH Terms:
    Cyclic AMP/*metabolism
    Epithelial Cells/*drug effects
    Kidney/*drug effects
    Polycystic Kidney, Autosomal Dominant/*drug therapy
    Propanolamines/*pharmacology
    Receptors, Adrenergic, beta-3/*chemistry
    Adrenergic beta-3 Receptor Antagonists/pharmacology ; Animals ; Case-Control Studies ; Cell Proliferation ; Cells, Cultured ; Epithelial Cells/metabolism ; Epithelial Cells/pathology ; Humans ; Kidney/metabolism ; Kidney/pathology ; Male ; Mice ; Mice, Knockout ; Polycystic Kidney, Autosomal Dominant/etiology ; Polycystic Kidney, Autosomal Dominant/metabolism ; Polycystic Kidney, Autosomal Dominant/pathology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Sphingomyelinase decreases transepithelial anion secretion in airway epithelial cells in part by inhibiting CFTR-mediated apical conductance.
    Autorzy:
    Cottrill KA; Molecular and Systems Pharmacology PhD Program, Emory University, Atlanta, Georgia, USA.
    Peterson RJ; Biochemistry, Cell, and Developmental Biology PhD Program, Emory University, Atlanta, Georgia, USA.
    Lewallen CF; Georgia Institute of Technology, G.W. Woodruff School of Mechanical Engineering, Atlanta, Georgia, USA.
    Koval M; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, Emory University, Atlanta, Georgia, USA.; Department of Cell Biology, Emory University, Atlanta, Georgia, USA.
    Bridges RJ; Department of Physiology and Biophysics, Center for Genetic Diseases, Chicago Medical School, North Chicago, Illinois, USA.
    McCarty NA; Molecular and Systems Pharmacology PhD Program, Emory University, Atlanta, Georgia, USA.; Department of Pediatrics and Children's Healthcare of Atlanta, Center for Cystic Fibrosis and Airways Disease Research, Emory University School of Medicine, Atlanta, Georgia, USA.
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    Źródło:
    Physiological reports [Physiol Rep] 2021 Aug; Vol. 9 (15), pp. e14928.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Anions/*metabolism
    Bronchi/*metabolism
    Cystic Fibrosis Transmembrane Conductance Regulator/*metabolism
    Epithelial Cells/*metabolism
    Sphingomyelin Phosphodiesterase/*metabolism
    Staphylococcus aureus/*enzymology
    Trachea/*metabolism
    Bronchi/cytology ; Cell Polarity ; Cells, Cultured ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics ; Epithelial Cells/cytology ; Humans ; Ion Transport ; Mutation ; Sphingomyelin Phosphodiesterase/genetics ; Trachea/cytology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Primary human mesothelial cell culture in the evaluation of the inflammatory response to different sclerosing agents used for pleurodesis.
    Autorzy:
    Mierzejewski M; Department of Internal Medicine, Pulmonary Diseases & Allergy, Medical University of Warsaw, Warsaw, Poland.
    Paplinska-Goryca M; Department of Internal Medicine, Pulmonary Diseases & Allergy, Medical University of Warsaw, Warsaw, Poland.
    Korczynski P; Department of Internal Medicine, Pulmonary Diseases & Allergy, Medical University of Warsaw, Warsaw, Poland.
    Krenke R; Department of Internal Medicine, Pulmonary Diseases & Allergy, Medical University of Warsaw, Warsaw, Poland.
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    Źródło:
    Physiological reports [Physiol Rep] 2021 Apr; Vol. 9 (8), pp. e14846.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Anti-Inflammatory Agents/*pharmacology
    Cytokines/*metabolism
    Epithelial Cells/*drug effects
    Pleura/*cytology
    Povidone-Iodine/*pharmacology
    Primary Cell Culture/*methods
    Sclerosing Solutions/*pharmacology
    Cell Line ; Cells, Cultured ; Cytokines/genetics ; Epithelial Cells/metabolism ; Humans ; Pleurodesis/methods ; Talc/toxicity
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Long noncoding RNA TINCR is a novel regulator of human bronchial epithelial cell differentiation state.
    Autorzy:
    Omote N; Pulmonary, Critical Care and Sleep Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
    Sakamoto K; Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.
    Li Q; Pulmonary, Critical Care and Sleep Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
    Schupp JC; Pulmonary, Critical Care and Sleep Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
    Adams T; Pulmonary, Critical Care and Sleep Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
    Ahangari F; Pulmonary, Critical Care and Sleep Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
    Chioccioli M; Pulmonary, Critical Care and Sleep Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
    DeIuliis G; Pulmonary, Critical Care and Sleep Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
    Hashimoto N; Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.
    Hasegawa Y; Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.; Department of Respiratory Medicine, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
    Kaminski N; Pulmonary, Critical Care and Sleep Medicine Section, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
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    Źródło:
    Physiological reports [Physiol Rep] 2021 Feb; Vol. 9 (3), pp. e14727.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Cell Differentiation*
    Bronchi/*metabolism
    Epithelial Cells/*metabolism
    RNA, Long Noncoding/*metabolism
    Bronchi/cytology ; Cell Movement ; Cell Proliferation ; Cells, Cultured ; Cytoskeletal Proteins/genetics ; Cytoskeletal Proteins/metabolism ; Gene Expression Regulation ; Humans ; Phenotype ; RNA, Long Noncoding/genetics ; RNA-Binding Proteins/genetics ; RNA-Binding Proteins/metabolism ; Receptors, Notch/genetics ; Receptors, Notch/metabolism ; SOXB1 Transcription Factors/genetics ; SOXB1 Transcription Factors/metabolism ; Signal Transduction
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Overexpression of Substance P in pig airways increases MUC5AC through an NF-kβ pathway.
    Autorzy:
    Sponchiado M; Department of Physiological Sciences, University of Florida, Gainesville, FL, USA.
    Liao YS; Department of Physiological Sciences, University of Florida, Gainesville, FL, USA.
    Atanasova KR; Department of Physiological Sciences, University of Florida, Gainesville, FL, USA.; Department of Medicinal Chemistry and Center for Natural Products, Drug Discovery and Development, University of Florida, Gainesville, FL, USA.
    Collins EN; Department of Physiological Sciences, University of Florida, Gainesville, FL, USA.
    Schurmann V; Department of Physiological Sciences, University of Florida, Gainesville, FL, USA.
    Bravo L; Department of Physiological Sciences, University of Florida, Gainesville, FL, USA.
    Reznikov LR; Department of Physiological Sciences, University of Florida, Gainesville, FL, USA.
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    Źródło:
    Physiological reports [Physiol Rep] 2021 Feb; Vol. 9 (3), pp. e14749.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural
    MeSH Terms:
    Epithelial Cells/*metabolism
    Inflammation Mediators/*metabolism
    Lung/*metabolism
    Mucin 5AC/*metabolism
    NF-kappa B/*metabolism
    Substance P/*metabolism
    Animals ; Animals, Newborn ; Bronchoconstriction ; Cells, Cultured ; Female ; Interleukin-10/genetics ; Interleukin-10/metabolism ; Lung/cytology ; Male ; Mucin 5AC/genetics ; Mucociliary Clearance ; Signal Transduction ; Substance P/genetics ; Sus scrofa ; Up-Regulation
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Alteration of chemokine production in bovine endometrial epithelial and stromal cells under heat stress conditions.
    Autorzy:
    Sakai S; Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
    Hatabu T; Laboratory of Animal Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
    Yamamoto Y; Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
    Kimura K; Laboratory of Reproductive Physiology, Graduate School of Environmental and Life Science, Okayama University, Okayama, Japan.
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    Źródło:
    Physiological reports [Physiol Rep] 2020 Nov; Vol. 8 (22), pp. e14640.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Heat-Shock Response*
    Chemokine CCL2/*metabolism
    Endometrium/*metabolism
    Epithelial Cells/*metabolism
    Interleukin-6/*metabolism
    Animals ; Cattle ; Cells, Cultured ; Endometrium/cytology ; Female ; Macrophages/metabolism ; Stromal Cells/metabolism
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Multiple calcium sources are required for intracellular calcium mobilization during gastric organoid epithelial repair.
    Autorzy:
    Engevik KA; Department of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.
    Karns RA; Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
    Oshima Y; Biomedical Optics Lab, Graduate School of Biomedical Engineering, Tohoku University, Miyagi, Japan.
    Montrose MH; Department of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.
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    Źródło:
    Physiological reports [Physiol Rep] 2020 Mar; Vol. 8 (5), pp. e14384.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Calcium/*metabolism
    Calcium Signaling/*physiology
    Epithelial Cells/*metabolism
    Gastric Mucosa/*metabolism
    Wound Healing/*physiology
    Animals ; Inositol 1,4,5-Trisphosphate Receptors/metabolism ; Mice, Inbred C57BL ; Mice, Transgenic ; Organoids ; Type C Phospholipases/metabolism
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Transcriptomic and barrier responses of human airway epithelial cells exposed to cannabis smoke.
    Autorzy:
    Aguiar JA; Department of Biology, University of Waterloo, Waterloo, Ontario, Canada.
    Huff RD; Division of Respiratory Medicine, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
    Tse W; Division of Respiratory Medicine, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
    Stämpfli MR; Firestone Institute for Respiratory Health - Division of Respirology, Department of Medicine, McMaster University, Hamilton, Ontario.
    McConkey BJ; Department of Biology, University of Waterloo, Waterloo, Ontario, Canada.; Firestone Institute for Respiratory Health - Division of Respirology, Department of Medicine, McMaster University, Hamilton, Ontario.
    Doxey AC; Department of Biology, University of Waterloo, Waterloo, Ontario, Canada.; Firestone Institute for Respiratory Health - Division of Respirology, Department of Medicine, McMaster University, Hamilton, Ontario.
    Hirota JA; Department of Biology, University of Waterloo, Waterloo, Ontario, Canada.; Division of Respiratory Medicine, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.; Firestone Institute for Respiratory Health - Division of Respirology, Department of Medicine, McMaster University, Hamilton, Ontario.
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    Źródło:
    Physiological reports [Physiol Rep] 2019 Oct; Vol. 7 (20), pp. e14249.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Marijuana Smoking*
    Tobacco Smoke Pollution*
    Transcriptome*
    Epithelial Cells/*metabolism
    Respiratory Mucosa/*metabolism
    Cell Line, Tumor ; Cell Survival/physiology ; Humans ; Smoke
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Novel lnc RNA regulated by HIF-1 inhibits apoptotic cell death in the renal tubular epithelial cells under hypoxia.
    Autorzy:
    Mimura I; Division of Nephrology and Endocrinology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
    Hirakawa Y; Division of Nephrology and Endocrinology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
    Kanki Y; Isotope Science Center, The University of Tokyo., Tokyo, Japan.
    Kushida N; Division of Nephrology and Endocrinology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
    Nakaki R; Division of GenomeScience, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
    Suzuki Y; Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.
    Tanaka T; Division of Nephrology and Endocrinology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
    Aburatani H; Division of GenomeScience, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
    Nangaku M; Division of Nephrology and Endocrinology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan .
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    Źródło:
    Physiological reports [Physiol Rep] 2017 Apr; Vol. 5 (8).
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Apoptosis*
    Epithelial Cells/*metabolism
    Hypoxia-Inducible Factor 1/*metabolism
    RNA, Long Noncoding/*genetics
    Cell Hypoxia ; Cell Line ; Epigenesis, Genetic ; Humans ; Kidney Tubules/cytology ; Protein Binding ; RNA, Long Noncoding/metabolism ; Response Elements ; Up-Regulation
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Cigarette smoke-induced urothelial cell damage: potential role of platelet-activating factor.
    Autorzy:
    Kispert SE; Department of Pathology, Saint Louis University School of Medicine, Saint Louis, Missouri.
    Marentette J; Department of Pathology, Saint Louis University School of Medicine, Saint Louis, Missouri.
    Campian EC; Department of Obstetrics, Gynecology & Women's Health, Saint Louis University School of Medicine, Saint Louis, Missouri.
    Isbell TS; Department of Pathology, Saint Louis University School of Medicine, Saint Louis, Missouri.
    Kuenzel H; Department of Pathology, Saint Louis University School of Medicine, Saint Louis, Missouri.
    McHowat J; Department of Pathology, Saint Louis University School of Medicine, Saint Louis, Missouri .
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    Źródło:
    Physiological reports [Physiol Rep] 2017 Mar; Vol. 5 (5).
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Smoke*
    Epithelial Cells/*drug effects
    Platelet Activating Factor/*metabolism
    Platelet Membrane Glycoproteins/*metabolism
    Receptors, G-Protein-Coupled/*metabolism
    Urothelium/*drug effects
    Animals ; Cell Line ; Epithelial Cells/cytology ; Epithelial Cells/metabolism ; Humans ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Smoking ; Urothelium/cytology ; Urothelium/metabolism ; Wound Healing/drug effects ; Wound Healing/physiology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    CRISPLD2 (LGL1) inhibits proinflammatory mediators in human fetal, adult, and COPD lung fibroblasts and epithelial cells.
    Autorzy:
    Zhang H; Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
    Kho AT; Children's Hospital Informatics Program Boston Children's Hospital, Boston, Massachusetts.
    Wu Q; Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
    Halayko AJ; Department of Physiology and Pathophysiology, University of Manitoba, Winnipeg, Manitoba, Canada Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada Biology of Breathing Group, Manitoba Institute of Child Health, Winnipeg, Manitoba, Canada.
    Limbert Rempel K; Department of Physiology and Pathophysiology, University of Manitoba, Winnipeg, Manitoba, Canada Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada Biology of Breathing Group, Manitoba Institute of Child Health, Winnipeg, Manitoba, Canada.
    Chase RP; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital Harvard Medical School, Boston, Massachusetts.
    Sweezey NB; The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada Departments of Paediatrics and Physiology, University of Toronto, Toronto, Ontario, Canada.
    Weiss ST; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital Harvard Medical School, Boston, Massachusetts.
    Kaplan F; Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada Departments of Human Genetics and Pediatrics, McGill University, Montreal, Quebec, Canada .
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    Źródło:
    Physiological reports [Physiol Rep] 2016 Sep; Vol. 4 (17).
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Bronchopulmonary Dysplasia/*metabolism
    Cell Adhesion Molecules/*metabolism
    Epithelial Cells/*metabolism
    Fibroblasts/*metabolism
    Inflammation Mediators/*antagonists & inhibitors
    Interferon Regulatory Factors/*metabolism
    Lung/*metabolism
    Pulmonary Disease, Chronic Obstructive/*metabolism
    Adult ; Aged ; Animals ; Bronchopulmonary Dysplasia/embryology ; Bronchopulmonary Dysplasia/pathology ; Cell Adhesion Molecules/deficiency ; Cell Adhesion Molecules/genetics ; Cell Proliferation/physiology ; Cells, Cultured ; Epithelial Cells/cytology ; Epithelial Cells/pathology ; Epithelial-Mesenchymal Transition/physiology ; Fibroblasts/cytology ; Fibroblasts/pathology ; HEK293 Cells ; Humans ; Inflammation Mediators/metabolism ; Interferon Regulatory Factors/deficiency ; Interferon Regulatory Factors/genetics ; Interleukin-6/metabolism ; Lipopolysaccharides/metabolism ; Lung/cytology ; Lung/embryology ; Lung/pathology ; Male ; Mice ; Middle Aged ; Pulmonary Disease, Chronic Obstructive/pathology ; Respiratory Mucosa/metabolism ; Respiratory Mucosa/pathology ; Signal Transduction
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Expression of polycomb protein BMI-1 maintains the plasticity of basal bronchial epithelial cells.
    Autorzy:
    Torr E; Division of Respiratory Medicine, Queens Medical Centre University of Nottingham, Nottingham, United Kingdom.
    Heath M; Cytogenetics Unit, Nottingham City Hospital, Hucknall Road, Nottingham, United Kingdom.
    Mee M; School of Life Sciences, Queens Medical Centre University of Nottingham, Nottingham, United Kingdom.
    Shaw D; Division of Respiratory Medicine, Queens Medical Centre University of Nottingham, Nottingham, United Kingdom.
    Sharp TV; Centre for Molecular Oncology, Barts Cancer Institute Queen Mary University of London, London, United Kingdom.
    Sayers I; Division of Respiratory Medicine, Queens Medical Centre University of Nottingham, Nottingham, United Kingdom .
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    Źródło:
    Physiological reports [Physiol Rep] 2016 Aug; Vol. 4 (16).
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Bronchi/*cytology
    Cell Plasticity/*genetics
    Epithelial Cells/*metabolism
    Polycomb Repressive Complex 1/*metabolism
    Adult ; Cell Differentiation/genetics ; Cell Differentiation/physiology ; Cellular Senescence/genetics ; Genes, p16 ; Genetic Engineering/methods ; Humans ; In Vitro Techniques ; Karyotype ; Lentivirus/genetics ; Male ; Middle Aged ; Peptide Fragments/metabolism ; Retroviridae/genetics ; Telomerase/metabolism
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    ADAM17 and EGFR regulate IL-6 receptor and amphiregulin mRNA expression and release in cigarette smoke-exposed primary bronchial epithelial cells from patients with chronic obstructive pulmonary disease (COPD).
    Autorzy:
    Stolarczyk M; Cell Biology, Erasmus MC, Rotterdam, The Netherlands.
    Amatngalim GD; Pulmonology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
    Yu X; Cell Biology, Erasmus MC, Rotterdam, The Netherlands.
    Veltman M; Cell Biology, Erasmus MC, Rotterdam, The Netherlands.
    Hiemstra PS; Pulmonology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
    Scholte BJ; Cell Biology, Erasmus MC, Rotterdam, The Netherlands .
    Pokaż więcej
    Źródło:
    Physiological reports [Physiol Rep] 2016 Aug; Vol. 4 (16).
    Typ publikacji:
    Journal Article
    MeSH Terms:
    ADAM17 Protein/*genetics
    Bronchi/*cytology
    Epithelial Cells/*metabolism
    ErbB Receptors/*genetics
    Pulmonary Disease, Chronic Obstructive/*metabolism
    RNA, Messenger/*genetics
    Receptors, Interleukin-6/*metabolism
    Smoking/*metabolism
    Aged ; Airway Remodeling ; Amphiregulin ; Female ; Humans ; Inhalation Exposure ; Male ; Middle Aged ; Pulmonary Disease, Chronic Obstructive/physiopathology ; Quinazolines/administration & dosage ; Quinazolines/adverse effects ; Quinazolines/metabolism ; Signal Transduction ; Smoking/adverse effects ; Nicotiana/adverse effects ; Tyrphostins/administration & dosage ; Tyrphostins/adverse effects ; Tyrphostins/metabolism
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Posttranscriptional regulation of 14-3-3ζ by RNA-binding protein HuR modulating intestinal epithelial restitution after wounding.
    Autorzy:
    Hansraj NZ; Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland.
    Xiao L; Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland Baltimore Veterans Affairs Medical Center, Baltimore, Maryland.
    Wu J; Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland.
    Chen G; Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland.
    Turner DJ; Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland Baltimore Veterans Affairs Medical Center, Baltimore, Maryland.
    Wang JY; Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland Baltimore Veterans Affairs Medical Center, Baltimore, Maryland Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland.
    Rao JN; Cell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland Baltimore Veterans Affairs Medical Center, Baltimore, Maryland .
    Pokaż więcej
    Źródło:
    Physiological reports [Physiol Rep] 2016 Jul; Vol. 4 (13).
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
    MeSH Terms:
    Protein Processing, Post-Translational*
    Re-Epithelialization*
    14-3-3 Proteins/*metabolism
    ELAV-Like Protein 1/*metabolism
    Epithelial Cells/*metabolism
    Intestinal Mucosa/*metabolism
    Molecular Chaperones/*metabolism
    14-3-3 Proteins/genetics ; 3' Untranslated Regions ; Animals ; Base Sequence ; Caco-2 Cells ; Cell Movement ; ELAV-Like Protein 1/deficiency ; ELAV-Like Protein 1/genetics ; Epithelial Cells/pathology ; Gene Expression Regulation ; Humans ; Intestinal Mucosa/pathology ; Mice, Knockout ; Molecular Chaperones/genetics ; Molecular Sequence Data ; RNA Interference ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Rats ; Signal Transduction ; Time Factors ; Transfection
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Non-neuronal, but atropine-sensitive ileal contractile responses to short-chain fatty acids: age-dependent desensitization and restoration under inflammatory conditions in mice.
    Autorzy:
    Yajima M; Laboratory of Histology and Cytology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan Laboratory of Physiology, School of Food and Nutritional Sciences, Graduate Division of Nutritional and Environmental Sciences, University of Shizuoka, Shizuoka, Japan Meiji Dairies Research Chair, Creative Research Institution, Hokkaido University, Sapporo, Japan .
    Kimura S; Laboratory of Histology and Cytology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
    Karaki S; Laboratory of Physiology, School of Food and Nutritional Sciences, Graduate Division of Nutritional and Environmental Sciences, University of Shizuoka, Shizuoka, Japan.
    Nio-Kobayashi J; Laboratory of Histology and Cytology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
    Tsuruta T; Meiji Dairies Research Chair, Creative Research Institution, Hokkaido University, Sapporo, Japan Department of Animal Science, Graduate School of Natural Science and Technology, Okayama University, Okayama, Japan.
    Kuwahara A; Laboratory of Physiology, School of Food and Nutritional Sciences, Graduate Division of Nutritional and Environmental Sciences, University of Shizuoka, Shizuoka, Japan.
    Yajima T; Laboratory of Histology and Cytology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan Meiji Dairies Research Chair, Creative Research Institution, Hokkaido University, Sapporo, Japan.
    Iwanaga T; Laboratory of Histology and Cytology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
    Pokaż więcej
    Źródło:
    Physiological reports [Physiol Rep] 2016 Apr; Vol. 4 (7).
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Atropine/*pharmacology
    Epithelial Cells/*drug effects
    Fatty Acids/*pharmacology
    Ileum/*drug effects
    Inflammation/*physiopathology
    Intestinal Mucosa/*drug effects
    Muscle Contraction/*drug effects
    Muscle, Smooth/*drug effects
    Acetic Acid/pharmacology ; Acetylcholine/metabolism ; Acetylcholinesterase/genetics ; Acetylcholinesterase/metabolism ; Age Factors ; Animals ; Choline O-Acetyltransferase/genetics ; Choline O-Acetyltransferase/metabolism ; Cholinesterase Inhibitors/pharmacology ; Disease Models, Animal ; Epithelial Cells/metabolism ; GPI-Linked Proteins/antagonists & inhibitors ; GPI-Linked Proteins/genetics ; GPI-Linked Proteins/metabolism ; Ileum/metabolism ; Ileum/physiopathology ; Inflammation/chemically induced ; Inflammation/genetics ; Inflammation/metabolism ; Intestinal Mucosa/metabolism ; Lipopolysaccharides ; Male ; Membrane Transport Proteins/genetics ; Membrane Transport Proteins/metabolism ; Mice, Inbred BALB C ; Muscle, Smooth/metabolism ; Muscle, Smooth/physiopathology ; Propionates/pharmacology ; Receptors, G-Protein-Coupled/agonists ; Receptors, G-Protein-Coupled/genetics ; Receptors, G-Protein-Coupled/metabolism ; Time Factors
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Enhancement in cellular Na+K+ATPase activity by low doses of peroxynitrite in mouse renal tissue and in cultured HK2 cells.
    Autorzy:
    Maiti AK; Department of Physiology, Hypertension and Renal Center of Excellence, Tulane University Health Sciences Center, New Orleans, Louisiana.
    Islam MT; Department of Physiology, Hypertension and Renal Center of Excellence, Tulane University Health Sciences Center, New Orleans, Louisiana.
    Satou R; Department of Physiology, Hypertension and Renal Center of Excellence, Tulane University Health Sciences Center, New Orleans, Louisiana.
    Majid DS; Department of Physiology, Hypertension and Renal Center of Excellence, Tulane University Health Sciences Center, New Orleans, Louisiana .
    Pokaż więcej
    Źródło:
    Physiological reports [Physiol Rep] 2016 Apr; Vol. 4 (7). Date of Electronic Publication: 2016 Apr 13.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Cell Membrane/*drug effects
    Enzyme Activators/*pharmacology
    Epithelial Cells/*drug effects
    Kidney Tubules, Proximal/*drug effects
    Peroxynitrous Acid/*pharmacology
    Sodium-Potassium-Exchanging ATPase/*metabolism
    Animals ; Cell Line ; Cell Membrane/enzymology ; Dose-Response Relationship, Drug ; Enzyme Inhibitors/pharmacology ; Epithelial Cells/enzymology ; Free Radical Scavengers/pharmacology ; Humans ; Kidney Tubules, Proximal/enzymology ; Mice, Inbred C57BL ; Nitric Oxide/metabolism ; Sodium-Potassium-Exchanging ATPase/antagonists & inhibitors ; Time Factors
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
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