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dc.contributor.authorStefani, Carolina Bernardi
dc.contributor.authorOliveira, Rafael Martins de
dc.contributor.authorSilveira, Angélica Aparecida Antoniellis
dc.contributor.authorFerraz, Lucio Fabio Caldas
dc.contributor.authorRibeiro, Marcelo Lima
dc.contributor.authorGambero, Alessandra
dc.contributor.authorPedrazzoli , Júnior, José
dc.date.accessioned2025-04-09T18:27:30Z
dc.date.available2025-04-09T18:27:30Z
dc.date.issued2012
dc.identifier.urihttp://repositorio.sis.puc-campinas.edu.br/xmlui/handle/123456789/17792
dc.description.abstractIntroduction Enterocromaffin-like cells (ECL) are specialized endocrine gastric cells able to release histamine, which in turn controls gastric acid production by parietal cells. Helicobacter pylori infection and other conditions signal in the gastrointestinal tract via Toll-like receptors (TLRs) and modify gastric acid production, but there is no evidence of expression and function of TLRs in ECL cells. In this work, we analyzed gene and protein expression of TLR-2, 4, 5, and 9, and other molecules involved in TLR signaling in ECL cells. Material and Methods ECL cells were isolated from Sprague–Dawley rats. The histamine-releasing ability of TLR ligands was also evaluated after culture of the ECL cells for a short time. Results With ECL cells that expressed the TLR-2, TLR-4, TLR-5, and TLR-9 genes we were able to confirm protein expression for TLR-2, TLR-5, and TLR-9. Functionally, ECL cells were able to release histamine in response to TLR-2 stimulation by peptidoglycan (PGN), a TLR-2 ligand. After PGN stimulus, IRAK and p38 phosphorylation could be observed. SB 203580, a p38 inhibitor, reversed PGN-induced histamine release. Lipopolysaccharide (LPS), a TLR-4 ligand, was also able to induce histamine release in ECL cells, but by a mechanism independent of TLRs. Conclusions We have demonstrated for the first time that ECL cells express TLRs and respond to TLR-2 ligand by increasing histamine release. This response could be involved in host defense against gastrointestinal bacterial pathogens but could also contribute to control of gastric acid secretion in the absence of pathogens.
dc.description.sponsorshipFAPESP (Fundação de Amparo à Pesquisa do Estado de São Paulo)
dc.language.isoInglês
dc.publisherSpringer Science and Business Media LLCpt_BR
dc.rightsAcesso abertopt_BR
dc.subjectLipopolysaccharide
dc.subjectPeptidoglycan
dc.subjectGastric secretion
dc.subjectp38
dc.subjectSignaling pathways
dc.titleExpression of Toll-Like receptors in enterocromaffin-like cells and their function in histamine releasept_BR
dc.typeArtigopt_BR
dc.contributor.institutionPontifícia Universidade Católica de Campinas (PUC-Campinas)pt_BR
dc.identifier.doihttps://doi.org/10.1007/s10620-012-2176-6pt_BR
dc.identifier.lattes7165708428659026pt_BR


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