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CYR61 (CCN1) overexpression induces lung injury in mice.
Grazioli, Serge; Gil, Sucheol; An, Dowon; Kajikawa, Osamu; Farnand, Alex W; Hanson, Josiah F; Birkland, Timothy; Chen, Peter; Duffield, Jeremy; Schnapp, Lynn M; Altemeier, William A; Matute-Bello, Gustavo.
Afiliação
  • Grazioli S; Pediatric Critical Care Unit, University Hospital of Geneva, Geneva, Switzerland; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Gil S; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • An D; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Kajikawa O; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Farnand AW; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Hanson JF; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Birkland T; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Chen P; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Duffield J; Division of Nephrology, Department of Medicine, University of Washington, Seattle, Washington;
  • Schnapp LM; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Altemeier WA; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington;
  • Matute-Bello G; Center for Lung Biology, Division of Pulmonary and Critical Medicine, Department of Medicine, University of Washington, Seattle, Washington; Veterans Affairs Puget Sound Healthcare System, Seattle, Washington.
Am J Physiol Lung Cell Mol Physiol ; 308(8): L759-65, 2015 Apr 15.
Article em En | MEDLINE | ID: mdl-25713320
ABSTRACT
Cysteine-rich protein-61 (CYR61), also known as connective tissue growth factor, CYR61, and nephroblastoma overexpressed gene 1 (CCN1), is a heparin-binding protein member of the CCN family of matricellular proteins. Gene expression profiles showed that Cyr61 is upregulated in human acute lung injury (ALI), but its functional role is unclear. We hypothesized that CYR61 contributes to ALI in mice. First, we demonstrated that CYR61 expression increases after bleomycin-induced lung injury. We then used adenovirus-mediated gene transfer to determine whether CYR61 overexpression in the lungs was sufficient to cause ALI. Mice instilled with CYR61 adenovirus showed greater weight loss, increased bronchoalveolar lavage total neutrophil counts, increased protein concentrations, and increased mortality compared with mice instilled with empty-vector adenovirus. Immunohistochemical studies in lungs from humans with idiopathic pulmonary fibrosis revealed CYR61 expression on the luminal membrane of alveolar epithelial cells in areas of injury. We conclude that CYR61 is upregulated in ALI and that CYR61 overexpression exacerbates ALI in mice.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Expressão Gênica / Lesão Pulmonar Aguda / Proteína Rica em Cisteína 61 Limite: Animals / Humans / Male Idioma: En Revista: Am J Physiol Lung Cell Mol Physiol Assunto da revista: BIOLOGIA MOLECULAR / FISIOLOGIA Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Expressão Gênica / Lesão Pulmonar Aguda / Proteína Rica em Cisteína 61 Limite: Animals / Humans / Male Idioma: En Revista: Am J Physiol Lung Cell Mol Physiol Assunto da revista: BIOLOGIA MOLECULAR / FISIOLOGIA Ano de publicação: 2015 Tipo de documento: Article