RESUMO
Helicobacter pylori infects the human stomach and causes a spectrum of disease that includes gastritis, peptic ulcers, and gastric adenocarcinoma. A chronic, neutrophil-rich inflammatory response characterizes this infection. It is established that H. pylori stimulates neutrophil chemotaxis and a robust respiratory burst, but other aspects of this interaction are incompletely defined. We demonstrate here that H. pylori induces N1-like subtype differentiation of human neutrophils as indicated by profound nuclear hypersegmentation, a CD62Ldim, CD16bright, CD11bbright, CD66bbright, CD63bright surface phenotype, proinflammatory cytokine secretion, and cytotoxicity. Hypersegmentation requires direct neutrophil-H. pylori contact as well as transcription and both host and bacterial protein synthesis, but not urease, NapA, VacA, CagA, or CagT. The concept of neutrophil plasticity is new and, to our knowledge, these data are the first evidence that neutrophils can undergo subtype differentiation in vitro in response to bacterial pathogen infection. We hypothesize that these changes favor H. pylori persistence and disease.
Assuntos
Helicobacter pylori/fisiologia , Interações Hospedeiro-Patógeno , Neutrófilos/microbiologia , Neutrófilos/fisiologia , Antígenos CD/genética , Antígenos CD/imunologia , Proteínas de Bactérias/genética , Diferenciação Celular , Núcleo Celular/ultraestrutura , Citocinas/imunologia , Citocinas/metabolismo , Humanos , Transtornos Leucocíticos , Neutrófilos/imunologia , Neutrófilos/ultraestrutura , Fenótipo , Urease/genéticaRESUMO
Both 3-farnesyl salicylic acid and 3-geranyl salicylic acid were synthesized from 2,6-dibromophenol and showed low levels of antimicrobial activity against E. coli strains.
