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Endothelial injury triggers a Ca2+ wave comprising peak and plateau phases with distinct mechanisms of intracellular store depletion and Ca2+ influx, resulting in nitric oxide generation. Connexin hemichannels play a crucial role in regulating this process, as blocking them reduces injury-induced nitric oxide production. Connexin mimetic peptides show promise in mitigating Ca2+ elevation and nitric oxide synthesis in aortic endothelial cells, offering potential therapeutic implications.
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Connexin hemichannels-mediated Ca2+ entry results in nitric oxide production in in situ injured endothelial cells Everardo Avelino Secondo anno Ciclo XXII
Introduction Injury provokes a Ca2+ wave characterized by two phases, peak and plateau PEAK ~ 60% > intracellular stores depletion (P2Y1,2,12,13) ~ 40 > Ca2+ influx (P2X and Gap junctions) PLATEAU Ca2+ influx (Gap junctions)
Introduction • Endothelium functions: • Angiogenesis and vasculogenesis • Preserve a surface unreactive toward circulating cells • Mantain thromboresistence • Inhibit vascular tone • Inhibit cells growth in outer layer of the vesell wall.
Nitric oxide measurement DAF FM DA Fluorescent dye Indicator of NO production Emission: 510nm Excitation: 490nm
Injury augments nitric oxide production in rat aortic endothelium
Injury augments nitric oxide production in rat aortic endothelium
Injury induced NOP* depend on extracellular Ca2+ * Nitric oxide production
Putative blockers of CxHcs* reduce NO synthesis induced by Ca2+ entry in injured endothelium *Connexin hemichannels
Putative blockers of CxHcs* reduce NO synthesis induced by Ca2+ entry in injured endothelium *Connexin hemichannels
Connexin mimetic peptides reduce both injury-induced Ca2+ elevation and NO production in ra aortic EC’s Pre-incubation
Connexin mimetic peptides reduce both injury-induced Ca2+ elevation and NO production in ra aortic EC’s Pre-incubation
Connexin mimetic peptides reduce both injury-induced Ca2+ elevation and NO production in ra aortic EC’s Accute effect
Connexin mimetic peptides reduce both injury-induced Ca2+ elevation and NO production in ra aortic EC’s
Summary ? Ca2+ ATPase ATP ATP Activates NCCE Inhibit CCE TRPV4 eNOS PLC PG ATP CaM IP3 Ca2+ Ca2+ Gap Ca2+ IP3R Intracellular Ca2+ stores Gap Nucleus Ca2+