dc.creator | Moreira, Vanessa | |
dc.creator | Lomonte, Bruno | |
dc.creator | Vinolo, Marco Aurélio Ramirez | |
dc.creator | Curi, Rui | |
dc.creator | Gutiérrez, José María | |
dc.creator | Teixeira, Catarina | |
dc.date | 2014 | |
dc.date | 2015-11-27T13:42:29Z | |
dc.date | 2015-11-27T13:42:29Z | |
dc.date.accessioned | 2018-03-29T01:20:42Z | |
dc.date.available | 2018-03-29T01:20:42Z | |
dc.identifier | Mediators Of Inflammation. v. 2014, p. 105879, 2014. | |
dc.identifier | 1466-1861 | |
dc.identifier | 10.1155/2014/105879 | |
dc.identifier | http://www.ncbi.nlm.nih.gov/pubmed/24808633 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/201384 | |
dc.identifier | 24808633 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1301617 | |
dc.description | Phospholipases A2 (PLA2) are key enzymes for production of lipid mediators. We previously demonstrated that a snake venom sPLA2 named MT-III leads to prostaglandin (PG)E2 biosynthesis in macrophages by inducing the expression of cyclooxygenase-2 (COX-2). Herein, we explored the molecular mechanisms and signaling pathways leading to these MT-III-induced effects. Results demonstrated that MT-III induced activation of the transcription factor NF-κB in isolated macrophages. By using NF-κB selective inhibitors, the involvement of this factor in MT-III-induced COX-2 expression and PGE2 production was demonstrated. Moreover, MT-III-induced COX-2 protein expression and PGE2 release were attenuated by pretreatment of macrophages with SB202190, and Ly294002, and H-7-dihydro compounds, indicating the involvement of p38MAPK, PI3K, and PKC pathways, respectively. Consistent with this, MT-III triggered early phosphorylation of p38MAPK, PI3K, and PKC. Furthermore, SB202190, H-7-dihydro, but not Ly294002 treatment, abrogated activation of NF-κB induced by MT-III. Altogether, these results show for the first time that the induction of COX-2 protein expression and PGE2 release, which occur via NF-κB activation induced by the sPLA2-MT-III in macrophages, are modulated by p38MAPK and PKC, but not by PI3K signaling proteins. | |
dc.description | 2014 | |
dc.description | 105879 | |
dc.language | eng | |
dc.relation | Mediators Of Inflammation | |
dc.relation | Mediators Inflamm. | |
dc.rights | aberto | |
dc.rights | | |
dc.source | PubMed | |
dc.subject | Animals | |
dc.subject | Cells, Cultured | |
dc.subject | Chromones | |
dc.subject | Cyclooxygenase 2 | |
dc.subject | Dinoprostone | |
dc.subject | Imidazoles | |
dc.subject | Macrophages | |
dc.subject | Male | |
dc.subject | Mice | |
dc.subject | Morpholines | |
dc.subject | Nf-kappa B | |
dc.subject | Phospholipases A2 | |
dc.subject | Protein Kinase C | |
dc.subject | Pyridines | |
dc.subject | Snake Venoms | |
dc.subject | P38 Mitogen-activated Protein Kinases | |
dc.title | An Asp49 Phospholipase A2 From Snake Venom Induces Cyclooxygenase-2 Expression And Prostaglandin E2 Production Via Activation Of Nf-κb, P38mapk, And Pkc In Macrophages. | |
dc.type | Artículos de revistas | |