Matches in SemOpenAlex for { <https://semopenalex.org/work/W2051848340> ?p ?o ?g. }
- W2051848340 endingPage "2501" @default.
- W2051848340 startingPage "2491" @default.
- W2051848340 abstract "Background— Secretoneurin is a neuropeptide located in nerve fibers along blood vessels, is upregulated by hypoxia, and induces angiogenesis. We tested the hypothesis that secretoneurin gene therapy exerts beneficial effects in a rat model of myocardial infarction and evaluated the mechanism of action on coronary endothelial cells. Methods and Results— In vivo secretoneurin improved left ventricular function, inhibited remodeling, and reduced scar formation. In the infarct border zone, secretoneurin induced coronary angiogenesis, as shown by increased density of capillaries and arteries. In vitro secretoneurin induced capillary tubes, stimulated proliferation, inhibited apoptosis, and activated Akt and extracellular signal-regulated kinase in coronary endothelial cells. Effects were abrogated by a vascular endothelial growth factor (VEGF) antibody, and secretoneurin stimulated VEGF receptors in these cells. Secretoneurin furthermore increased binding of VEGF to endothelial cells, and binding was blocked by heparinase, indicating that secretoneurin stimulates binding of VEGF to heparan sulfate proteoglycan binding sites. Additionally, secretoneurin increased binding of VEGF to its coreceptor neuropilin-1. In endothelial cells, secretoneurin also stimulated fibroblast growth factor receptor-3 and insulin-like growth factor-1 receptor, and in coronary vascular smooth muscle cells, we observed stimulation of VEGF receptor-1 and fibroblast growth factor receptor-3. Exposure of cardiac myocytes to hypoxia and ischemic heart after myocardial infarction revealed increased secretoneurin messenger RNA and protein. Conclusions— Our data show that secretoneurin acts as an endogenous stimulator of VEGF signaling in coronary endothelial cells by enhancing binding of VEGF to low-affinity binding sites and neuropilin-1 and stimulates further growth factor receptors like fibroblast growth factor receptor-3. Our in vivo findings indicate that secretoneurin may be a promising therapeutic tool in ischemic heart disease." @default.
- W2051848340 created "2016-06-24" @default.
- W2051848340 creator A5005446581 @default.
- W2051848340 creator A5007410452 @default.
- W2051848340 creator A5014823061 @default.
- W2051848340 creator A5015655934 @default.
- W2051848340 creator A5018292189 @default.
- W2051848340 creator A5020084134 @default.
- W2051848340 creator A5024396516 @default.
- W2051848340 creator A5028567131 @default.
- W2051848340 creator A5031707276 @default.
- W2051848340 creator A5041895189 @default.
- W2051848340 creator A5043989944 @default.
- W2051848340 creator A5045030140 @default.
- W2051848340 creator A5049348856 @default.
- W2051848340 creator A5062003804 @default.
- W2051848340 creator A5066346307 @default.
- W2051848340 creator A5083861048 @default.
- W2051848340 creator A5087916167 @default.
- W2051848340 creator A5090820164 @default.
- W2051848340 creator A5090898004 @default.
- W2051848340 date "2012-11-20" @default.
- W2051848340 modified "2023-10-17" @default.
- W2051848340 title "The Angiogenic Factor Secretoneurin Induces Coronary Angiogenesis in a Model of Myocardial Infarction by Stimulation of Vascular Endothelial Growth Factor Signaling in Endothelial Cells" @default.
- W2051848340 cites W122651877 @default.
- W2051848340 cites W145648313 @default.
- W2051848340 cites W1562216431 @default.
- W2051848340 cites W1754620482 @default.
- W2051848340 cites W1977387194 @default.
- W2051848340 cites W1991362893 @default.
- W2051848340 cites W1992112921 @default.
- W2051848340 cites W1999171451 @default.
- W2051848340 cites W2014368942 @default.
- W2051848340 cites W2014608793 @default.
- W2051848340 cites W2028172989 @default.
- W2051848340 cites W2036607811 @default.
- W2051848340 cites W2037519944 @default.
- W2051848340 cites W2067825063 @default.
- W2051848340 cites W2087436793 @default.
- W2051848340 cites W2089029717 @default.
- W2051848340 cites W2098902079 @default.
- W2051848340 cites W2124715674 @default.
- W2051848340 cites W2125150769 @default.
- W2051848340 cites W2138868579 @default.
- W2051848340 cites W2140449419 @default.
- W2051848340 cites W2144804597 @default.
- W2051848340 cites W2150464881 @default.
- W2051848340 cites W2152843042 @default.
- W2051848340 cites W2167661646 @default.
- W2051848340 cites W2168884406 @default.
- W2051848340 cites W2170950673 @default.
- W2051848340 doi "https://doi.org/10.1161/circulationaha.111.076950" @default.
- W2051848340 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3839617" @default.
- W2051848340 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23081990" @default.
- W2051848340 hasPublicationYear "2012" @default.
- W2051848340 type Work @default.
- W2051848340 sameAs 2051848340 @default.
- W2051848340 citedByCount "86" @default.
- W2051848340 countsByYear W20518483402013 @default.
- W2051848340 countsByYear W20518483402014 @default.
- W2051848340 countsByYear W20518483402015 @default.
- W2051848340 countsByYear W20518483402016 @default.
- W2051848340 countsByYear W20518483402017 @default.
- W2051848340 countsByYear W20518483402018 @default.
- W2051848340 countsByYear W20518483402019 @default.
- W2051848340 countsByYear W20518483402020 @default.
- W2051848340 countsByYear W20518483402021 @default.
- W2051848340 countsByYear W20518483402022 @default.
- W2051848340 countsByYear W20518483402023 @default.
- W2051848340 crossrefType "journal-article" @default.
- W2051848340 hasAuthorship W2051848340A5005446581 @default.
- W2051848340 hasAuthorship W2051848340A5007410452 @default.
- W2051848340 hasAuthorship W2051848340A5014823061 @default.
- W2051848340 hasAuthorship W2051848340A5015655934 @default.
- W2051848340 hasAuthorship W2051848340A5018292189 @default.
- W2051848340 hasAuthorship W2051848340A5020084134 @default.
- W2051848340 hasAuthorship W2051848340A5024396516 @default.
- W2051848340 hasAuthorship W2051848340A5028567131 @default.
- W2051848340 hasAuthorship W2051848340A5031707276 @default.
- W2051848340 hasAuthorship W2051848340A5041895189 @default.
- W2051848340 hasAuthorship W2051848340A5043989944 @default.
- W2051848340 hasAuthorship W2051848340A5045030140 @default.
- W2051848340 hasAuthorship W2051848340A5049348856 @default.
- W2051848340 hasAuthorship W2051848340A5062003804 @default.
- W2051848340 hasAuthorship W2051848340A5066346307 @default.
- W2051848340 hasAuthorship W2051848340A5083861048 @default.
- W2051848340 hasAuthorship W2051848340A5087916167 @default.
- W2051848340 hasAuthorship W2051848340A5090820164 @default.
- W2051848340 hasAuthorship W2051848340A5090898004 @default.
- W2051848340 hasBestOaLocation W20518483401 @default.
- W2051848340 hasConcept C126322002 @default.
- W2051848340 hasConcept C134018914 @default.
- W2051848340 hasConcept C146285616 @default.
- W2051848340 hasConcept C14858245 @default.
- W2051848340 hasConcept C15215337 @default.
- W2051848340 hasConcept C167734588 @default.
- W2051848340 hasConcept C2777025900 @default.
- W2051848340 hasConcept C2780394083 @default.