Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases
Versión final del documento embargada hasta 2081-08 por política editorial
| Autores: | , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2011 |
| País: | Costa Rica |
| Institución: | Universidad de Costa Rica |
| Repositorio: | Kérwá |
| OAI Identifier: | oai:kerwa.ucr.ac.cr:10669/29556 |
| Acceso en línea: | http://www.sciencedirect.com/science/article/pii/S187439191100128X https://hdl.handle.net/10669/29556 http://dx.doi.org/10.1016/j.jprot.2011.03.026 |
| Access Level: | acceso embargado |
| Palabra clave: | Snake venom Metalloproteinases Hemorrhage Capillary vessels Basement membrane Disintegrin-like domain Cysteine-rich domain Collagens Perlecan Nidogen |
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| dc.title.es_ES.fl_str_mv |
Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases |
| title |
Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases |
| spellingShingle |
Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases Escalante Muñoz, Teresa Snake venom Metalloproteinases Hemorrhage Capillary vessels Basement membrane Disintegrin-like domain Cysteine-rich domain Collagens Perlecan Nidogen |
| title_short |
Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases |
| title_full |
Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases |
| title_fullStr |
Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases |
| title_full_unstemmed |
Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases |
| title_sort |
Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases |
| dc.creator.none.fl_str_mv |
Escalante Muñoz, Teresa Rucavado Romero, Alexandra Fox, Jay W. Gutiérrez, José María |
| author |
Escalante Muñoz, Teresa |
| author_facet |
Escalante Muñoz, Teresa Rucavado Romero, Alexandra Fox, Jay W. Gutiérrez, José María |
| author_role |
author |
| author2 |
Rucavado Romero, Alexandra Fox, Jay W. Gutiérrez, José María |
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author author author |
| dc.subject.es_ES.fl_str_mv |
Snake venom Metalloproteinases Hemorrhage Capillary vessels Basement membrane Disintegrin-like domain Cysteine-rich domain Collagens Perlecan Nidogen |
| topic |
Snake venom Metalloproteinases Hemorrhage Capillary vessels Basement membrane Disintegrin-like domain Cysteine-rich domain Collagens Perlecan Nidogen |
| description |
Versión final del documento embargada hasta 2081-08 por política editorial |
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2011 |
| dc.date.issued.none.fl_str_mv |
2011-08-24 |
| dc.date.accessioned.none.fl_str_mv |
2017-02-27T15:53:36Z |
| dc.date.available.none.fl_str_mv |
2017-02-27T15:53:36Z |
| dc.type.none.fl_str_mv |
artículo original http://purl.org/coar/resource_type/c_2df8fbb1 info:eu-repo/semantics/article |
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article |
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http://www.sciencedirect.com/science/article/pii/S187439191100128X |
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1874-3919 |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10669/29556 |
| dc.identifier.doi.none.fl_str_mv |
http://dx.doi.org/10.1016/j.jprot.2011.03.026 |
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741-A7-604 741-A7-502 741-B0-606 |
| dc.identifier.pmid.none.fl_str_mv |
21447411 |
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http://www.sciencedirect.com/science/article/pii/S187439191100128X https://hdl.handle.net/10669/29556 http://dx.doi.org/10.1016/j.jprot.2011.03.026 |
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1874-3919 741-A7-604 741-A7-502 741-B0-606 21447411 |
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en_US |
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en_US |
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acceso embargado http://purl.org/coar/access_right/c_f1cf info:eu-repo/semantics/embargoedAccess |
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acceso embargado http://purl.org/coar/access_right/c_f1cf |
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embargoedAccess |
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Journal of Proteomics; Volumen 74, Número 9, 2011 |
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reponame:Kérwá instname:Universidad de Costa Rica instacron:UCR |
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Escalante Muñoz, Teresa86d9e00a-76f8-4552-9d02-a03587d50166600Rucavado Romero, Alexandraf62bf3bf-c612-451f-90ef-a366ebb3f4b5600Fox, Jay W.9b8320ba-4241-4f7e-9982-b24409e85c45600Gutiérrez, José María6a9bac5f-130f-4977-8ddf-ab97fcafacc46002017-02-27T15:53:36Z2017-02-27T15:53:36Z2011-08-24http://www.sciencedirect.com/science/article/pii/S187439191100128X1874-3919https://hdl.handle.net/10669/29556http://dx.doi.org/10.1016/j.jprot.2011.03.026741-A7-604741-A7-502741-B0-60621447411Versión final del documento embargada hasta 2081-08 por política editorialHemorrhage is one of the most significant effects in envenomings induced by viperid snakebites. Damage to the microvasculature, induced by snake venom metalloproteinases (SVMPs), is the main event responsible for this effect. The precise mechanism by which SVMPs disrupt the microvasculature has remained elusive, although recent developments provide valuable clues to deciphering the details of this pathological effect. The main targets of hemorrhagic SVMPs are components of basement membrane (BM) and surrounding extracellular matrix (ECM), which provide mechanical stability to capillaries. P-III SVMPs, comprising disintegrin-like and cysteine-rich domains in addition to the catalytic domain, are more potent hemorrhagic toxins than P-I SVMPs, constituted only by the metalloproteinase domain. This is likely due to the presence of exosites in the additional domains, which contribute to the binding of SVMPs to relevant targets in the microvasculature. Recent in vivo studies have shown that P-III SVMPs are preferentially located in microvessels. On the other hand, the structural determinants responsible for the different hemorrhagic potential of P-I SVMPs remain largely unknown, although backbone flexibility in a loop located near the active site is likely to play a role. Moreover, hemorrhagic and non-hemorrhagic SVMPs differ in their capacity to hydrolyze in vivo key BM proteins, such as type IV collagen and perlecan, as well as other ECM proteins, like types VI and XV collagens, which play a critical role by connecting BM components to perivascular fibrillar collagens. The evidence gathered support a two-step model for the pathogenesis of SVMP-induced hemorrhage: initially, hemorrhagic SVMPs bind to and hydrolyze components of the BM and associated extracellular matrix proteins that play a key role in the mechanical stability of BM. In conditions of normal blood flow in the tissues, such cleavage results in the weakening, distension and eventual disruption of capillary wall due to the action of biophysical forces operating in vivo.Universidad de Costa Rica/[741-A7-604]/UCR/Costa RicaUniversidad de Costa Rica/[741-A7-502]/UCR/Costa RicaUniversidad de Costa Rica/[741-B0-606]/UCR/Costa RicaInternational Foundation for Science//IFS/SueciaOrganisation for the Prohibition of Chemical Weapons/[F/4096-1]/OPCW/Paises BajosNetwork for Research and Training in Tropical Diseases in Central America/[2-N-2008]/NeTropica/Network for Research and Training in Tropical Diseases in Central America/[01-N-2010]/NeTropica/University of Virginia School of Medicine//J.W.F./Estados UnidosUCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias de la Salud::Instituto Clodomiro Picado (ICP)en_USacceso embargadohttp://purl.org/coar/access_right/c_f1cfinfo:eu-repo/semantics/embargoedAccessJournal of Proteomics; Volumen 74, Número 9, 2011reponame:Kérwáinstname:Universidad de Costa Ricainstacron:UCRSnake venomMetalloproteinasesHemorrhageCapillary vesselsBasement membraneDisintegrin-like domainCysteine-rich domainCollagensPerlecanNidogenKey events in microvascular damage induced by snake venom hemorrhagic metalloproteinasesartículo originalhttp://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articleTHUMBNAIL320_2011_J.Proteomics_Escalante_SVMP_hemorrhage_review.pdf.jpg320_2011_J.Proteomics_Escalante_SVMP_hemorrhage_review.pdf.jpgGenerated Thumbnailimage/jpeg3556https://www.kerwa.ucr.ac.cr/bitstreams/56eb8c2b-0ba2-4381-92a3-7ddfd126ab3b/downloada63dfdd6bfe9f2199e0527add45d1bf6MD54ORIGINAL320_2011_J.Proteomics_Escalante_SVMP_hemorrhage_review.pdf320_2011_J.Proteomics_Escalante_SVMP_hemorrhage_review.pdfVersión finalapplication/pdf1924633https://www.kerwa.ucr.ac.cr/bitstreams/6e79f7c7-7f24-4a0d-8a98-c022e0a87362/downloadbc7a4426b2786ee92345404280cc66edMD51LICENSElicense.txtlicense.txttext/plain; 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