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Serine proteinases from Bothrops snake venom activates PI3K/Akt mediated angiogenesis

dc.contributor.authorBhat, Shreesha K.
dc.contributor.authorJoshi, Manjunath B.
dc.contributor.authorUllah, Anwar [UNESP]
dc.contributor.authorMasood, Rehana [UNESP]
dc.contributor.authorBiligiri, Setlur G.
dc.contributor.authorArni, Raghuvir K. [UNESP]
dc.contributor.authorSatyamoorthy, Kapaettu
dc.contributor.institutionManipal University
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionJagadale Industries
dc.date.accessioned2018-12-11T16:44:37Z
dc.date.available2018-12-11T16:44:37Z
dc.date.issued2016-12-15
dc.description.abstractThe discovery of rapid acting and powerful angiogenic proteins are of significant interest in the treatment of various human disorders associated with insufficient angiogenesis such as ischemia, menorrhagia and delayed wound healing. Snake venoms consist of a mixture of bioactive proteins and polypeptides and are rich sources of pharmacologically important molecules. Serine proteinases are one of the abundant proteins present in Bothrops snake venoms and possess multiple biological functions including the regulation of the blood coagulation cascade. In this study, serine proteinases from Bothrops atrox (B. atrox) and Bothrops brazili (B. brazili) that modulate angiogenesis were purified and characterized. Molecular size exclusion chromatography, affinity chromatography followed by ion exchange chromatography of the serine proteinases indicated molecular masses of around 32 kDa. Serine proteinases from both the species exhibited diverse catalytic activities such as the ability to induce amidolytic, fibrinogenolytic, gelatinolytic activities and also coagulated plasma with a minimal coagulation concentration of 2.4 μg/mL. Serine proteinases facilitated the sprouting of human umbilical vein endothelial cells (HUVEC) in three-dimensional culture systems and induced tubule formation in monolayer culture systems. Serine proteinase stimulated Aktser473 and eNOSser1177 phosphorylation in endothelial cells and addition of PI3K inhibitor LY294002 abrogated the effects of serine proteinases on sprout formation of endothelial cells in 3D collagen gels, suggesting that serine proteinase facilitated angiogenesis was mediated by PI3K/eNOS signaling axis. We also show in agarose plug assays using a mouse model, serine proteinases from Bothrops venoms significantly enhanced neovascularization. Our data suggests pro-angiogenic activity by the serine proteinases from B. atrox and B. brazili venom and further studies are warranted to explore the therapeutic applications.en
dc.description.affiliationSchool of Life Sciences Manipal University
dc.description.affiliationMultiuser Center for Biomolecular Innovation IBILCE/UNESP
dc.description.affiliationJuggat Pharma Jagadale Industries
dc.description.affiliationUnespMultiuser Center for Biomolecular Innovation IBILCE/UNESP
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2015/13765-0
dc.description.sponsorshipIdFAPESP: 401388/2013-1
dc.description.sponsorshipIdFAPESP: MCTI/CNPq/DBT
dc.format.extent63-72
dc.identifierhttp://dx.doi.org/10.1016/j.toxicon.2016.11.001
dc.identifier.citationToxicon, v. 124, p. 63-72.
dc.identifier.doi10.1016/j.toxicon.2016.11.001
dc.identifier.file2-s2.0-84994893799.pdf
dc.identifier.issn1879-3150
dc.identifier.issn0041-0101
dc.identifier.lattes9162508978945887
dc.identifier.orcid0000-0003-2460-1145
dc.identifier.scopus2-s2.0-84994893799
dc.identifier.urihttp://hdl.handle.net/11449/169137
dc.language.isoeng
dc.relation.ispartofToxicon
dc.relation.ispartofsjr0,692
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAngiogenesis
dc.subjectBlood coagulation
dc.subjectBothrops
dc.subjectSerine proteinases
dc.subjectTherapeutic applications
dc.subjectVenom
dc.titleSerine proteinases from Bothrops snake venom activates PI3K/Akt mediated angiogenesisen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.lattes9162508978945887[6]
unesp.author.orcid0000-0003-2460-1145[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt

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