dc.creatorMORANDINI, Ana Carolina F.
dc.creatorSIPERT, Carla Renata
dc.creatorGASPAROTO, Thais Helena
dc.creatorGREGHI, Sebastiao Luiz A.
dc.creatorPASSANEZI, Euloir
dc.creatorREZENDE, Maria Lucia R.
dc.creatorSANT`ANA, Adriana P.
dc.creatorCAMPANELLI, Ana Paula
dc.creatorGARLET, Gustavo P.
dc.creatorSANTOS, Carlos F.
dc.date.accessioned2012-10-20T00:57:47Z
dc.date.accessioned2018-07-04T15:25:18Z
dc.date.available2012-10-20T00:57:47Z
dc.date.available2018-07-04T15:25:18Z
dc.date.created2012-10-20T00:57:47Z
dc.date.issued2010
dc.identifierJOURNAL OF PERIODONTOLOGY, v.81, n.2, p.310-317, 2010
dc.identifier0022-3492
dc.identifierhttp://producao.usp.br/handle/BDPI/26077
dc.identifier10.1902/jop.2009.090375
dc.identifierhttp://dx.doi.org/10.1902/jop.2009.090375
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1622741
dc.description.abstractBackground: Fibroblasts are considered important cells in periodontitis. When challenged by different agents, they respond through the release of cytokines that participate in the inflammatory process. The aim of this study is to evaluate and compare the expression and production of macrophage inflammatory protein (MIP)-1 alpha, stromal-derived factor (SDF)-1, and interleukin (IL)-6 by human cultured periodontal ligament and gingival fibroblasts challenged with lipopolysaccharide (LPS) from Porphyromonas gingivalis. Methods: Fibroblasts were cultured from biopsies of gingival tissue and periodontal ligament of the same donors and used on the fourth passage. After confluence in 24-well plates, the culture medium alone (control) or with 0.1 to 10 mu g/ml of LPS from P. gingivalis was added to the wells, and after 1, 6, and 24 hours, the supernatant and the cells were collected and analyzed by enzyme-linked immunosorbent assay and real-time polymerase chain reaction, respectively. Results: MIP-1 alpha, SDF-1, and IL-6 protein production was significantly greater in gingival fibroblasts compared to periodontal ligament fibroblasts. IL-6 was upregulated in a time-dependent manner, mainly in gingival fibroblasts (P<0.05), which secreted more MIP-1 alpha in the lowest concentration of LPS used (0.1 mu g/ml). In contrast, a basal production of SDF-1 that was inhibited with the increase of LPS concentration was detected, especially after 24 hours (P<0.05). Conclusion: The distinct ability of the gingival and periodontal ligament fibroblasts to secrete MIP-1 alpha, SDF-1, and IL-6 emphasizes that these cells may differently contribute to the balance of cytokines in the LPS-challenged periodontium. J Periodontol 2010;81:310-317.
dc.languageeng
dc.publisherAMER ACAD PERIODONTOLOGY
dc.relationJournal of Periodontology
dc.rightsCopyright AMER ACAD PERIODONTOLOGY
dc.rightsrestrictedAccess
dc.subjectCytokines
dc.subjectfibroblasts
dc.subjectperiodontitis
dc.subjectPorphyromonas gingivalis
dc.titleDifferential Production of Macrophage Inflammatory Protein-1 alpha, Stromal-Derived Factor-1, and IL-6 by Human Cultured Periodontal Ligament and Gingival Fibroblasts Challenged With Lipopolysaccharide From P. gingivalis
dc.typeArtículos de revistas


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