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dc.contributor.author | Marcos, L.A. | |
dc.contributor.author | Terashima, A. | |
dc.contributor.author | Yi, P. | |
dc.contributor.author | Andrade, R. | |
dc.contributor.author | Cubero, F.J. | |
dc.contributor.author | Albanis, E. | |
dc.contributor.author | Gotuzzo Herencia, José Eduardo | |
dc.contributor.author | Espinoza, J.R. | |
dc.contributor.author | Friedman, S.L. | |
dc.date.accessioned | 2022-01-18T19:34:43Z | |
dc.date.available | 2022-01-18T19:34:43Z | |
dc.date.issued | 2011 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/11191 | |
dc.description.abstract | We have evaluated the possible mechanisms of liver fibrosis caused by Fasciola hepatica in an animal model and in culture using immortalized human stellate cells. Liver biopsies of F. hepatica-infected rats were performed at wk 8 and 16. Serum-starved LX-2 cells, a human stellate cell line, were exposed to increasing concentrations of Fas2 antigen. The expression of key fibrosis-related genes was evaluated by qRT-PCR. There was a significant correlation between fibrogenic gene expression and both intensity and duration of infection. LX-2 cells exposed to Fas2 showed progressively increased expression of mRNAs for Collagen I, alpha-smooth muscle-actin, platelet-derived growth factor beta receptor, and tissue inhibitor of metalloproteinase II; inhibition of Fas2 cysteine proteinase activity by E-64 abrogated these increases, suggesting that the protease activity of Fas2 is involved in fibrogenic stimulation. In summary, F. hepatica infection is associated with up-regulation of mRNAs associated with hepatic fibrogenesis in vivo and in activated hepatic stellate cells. | en_US |
dc.language.iso | eng | |
dc.publisher | American Society of Parasitologists | |
dc.relation.ispartofseries | Journal of Parasitology | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.subject | Humans|controlled study | en_US |
dc.subject | pathology | en_US |
dc.subject | animal | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | animal tissue | en_US |
dc.subject | Animals | en_US |
dc.subject | collagen type 1 | en_US |
dc.subject | genetics | en_US |
dc.subject | in vitro study | en_US |
dc.subject | in vivo study | en_US |
dc.subject | metabolism | en_US |
dc.subject | non|physiology | en_US |
dc.subject | pathogenicity | en_US |
dc.subject | polymerase chain reaction | en_US |
dc.subject | infectious disease | en_US |
dc.subject | parasite antigen | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | disease association | en_US |
dc.subject | gene expression | en_US |
dc.subject | Disease Models, Animal | en_US |
dc.subject | Analysis of Variance | en_US |
dc.subject | Cell Line | en_US |
dc.subject | messenger RNA | en_US |
dc.subject | upregulation | en_US |
dc.subject | disease model | en_US |
dc.subject | real time polymerase chain reaction | en_US |
dc.subject | enzymology | en_US |
dc.subject | tissue inhibitor of metalloproteinase 1 | en_US |
dc.subject | Fasciola hepatica | en_US |
dc.subject | Fascioliasis | en_US |
dc.subject | enzyme activity | en_US |
dc.subject | Animalia | en_US |
dc.subject | Antigens, Helminth | en_US |
dc.subject | cysteine proteinase | en_US |
dc.subject | Rats | en_US |
dc.subject | analysis of variance | en_US |
dc.subject | Gene Expression | en_US |
dc.subject | functional morphology | en_US |
dc.subject | genetic analysis | en_US |
dc.subject | numerical model | en_US |
dc.subject | gelatinase A | en_US |
dc.subject | experimental study | en_US |
dc.subject | transforming growth factor beta1 | en_US |
dc.subject | Rattus | en_US |
dc.subject | Actins | en_US |
dc.subject | alpha smooth muscle actin | en_US |
dc.subject | antigen | en_US |
dc.subject | cell activation | en_US |
dc.subject | cell organelle | en_US |
dc.subject | Collagen | en_US |
dc.subject | Cysteine Endopeptidases | en_US |
dc.subject | Fas antigen | en_US |
dc.subject | Fas2 antigen | en_US |
dc.subject | Fas2 antigen, Fasciola hepatica | en_US |
dc.subject | fibrogenesis | en_US |
dc.subject | flatworm | en_US |
dc.subject | Hepatic Stellate Cells | en_US |
dc.subject | inhibitor | en_US |
dc.subject | liver biopsy | en_US |
dc.subject | Liver Cirrhosis | en_US |
dc.subject | liver fibrosis | en_US |
dc.subject | n [n (3 carboxyoxirane 2 carbonyl)leucyl]agmatine | en_US |
dc.subject | platelet derived growth factor beta receptor | en_US |
dc.subject | Receptor, Platelet-Derived Growth Factor beta | en_US |
dc.subject | stellate cell | en_US |
dc.subject | tissue inhibitor of metalloproteinase 2 | en_US |
dc.subject | Tissue Inhibitor of Metalloproteinase-2 | en_US |
dc.title | Mechanisms of liver fibrosis associated with experimental fasciola hepatica infection: Roles of Fas2 proteinase and hepatic stellate cell activation | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1645/GE-2420.1 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.03.07 | |
dc.relation.issn | 1937-2345 |
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