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Authordc.contributor.authorTroncoso Cotal, Rodrigo Hernán 
Authordc.contributor.authorIbarra, Cristián es_CL
Authordc.contributor.authorVicencio, José Miguel es_CL
Authordc.contributor.authorJaimovich Pérez, Enrique es_CL
Authordc.contributor.authorLavandero González, Sergioes_CL
Admission datedc.date.accessioned2014-12-15T12:25:57Z
Available datedc.date.available2014-12-15T12:25:57Z
Publication datedc.date.issued2014
Cita de ítemdc.identifier.citationTrends in Endocrinology and Metabolism March 2014, Vol. 25, No. 3en_US
Identifierdc.identifier.otherdx.doi.org/10.1016/j.tem.2013.12.002
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121894
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractInsulin-like growth factor 1 (IGF-1) signaling regulates contractility, metabolism, hypertrophy, autophagy, senescence, and apoptosis in the heart. IGF-1 deficiency is associated with an increased risk of cardiovascular disease, whereas cardiac activation of IGF-1 receptor (IGF-1R) protects from the detrimental effects of a high-fat diet and myocardial infarction. IGF-1R activates multiple pathways through its intrinsic tyrosine kinase activity and through coupling to heterotrimeric G protein. These pathways involve classic second messengers, phosphorylation cascades, lipid signaling, Ca2+ transients, and gene expression. In addition, IGF-1R triggers signaling in different subcellular locations including the plasma membrane, perinuclear T tubules, and also in internalized vesicles. In this review, we provide a fresh and updated view of the complex IGF- 1 scenario in the heart, including a critical focus on therapeutic strategies.en_US
Patrocinadordc.description.sponsorshipThis work was supported by FONDECYT (grant 1120212 to S.L. and grant 11130285 to R.T.) and CONICYT (grant Anillo ACT 1111 to E.J. and S.L.; FONDAP 15130011 to S.L. and R.T.; Red 120003 to S.L.)en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevieren_US
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Keywordsdc.subjectIGF-1Ren_US
Títulodc.titleNew insights into IGF-1 signaling in the hearten_US
Document typedc.typeArtículo de revista


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile