Regulation of cardiac autophagy by insulin-like growth factor 1

Rodrigo Troncoso, Jessica Díaz-Elizondo, Sandra P. Espinoza, Mario F. Navarro-Marquez, Alejandra P. Oyarzún, Jaime A. Riquelme, Ivonne Garcia-Carvajal, Guillermo Díaz-Araya, Lorena García, Joseph A Hill, Sergio Lavandero

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Insulin-like growth factor-1 (IGF-1) signaling is a key pathway in the control of cell growth and survival. Three critical nodes in the IGF-1 signaling pathway have been described in cardiomyocytes: protein kinase Akt/mammalian target of rapamycin (mTOR), Ras/Raf/extracellular signal-regulated kinase (ERK), and phospholipase C (PLC)/inositol 1,4,5-triphosphate (InsP3)/ Ca2+. The Akt/mTOR and Ras/Raf/ERK signaling arms govern survival in the settings of cardiac stress and hypertrophic growth. By contrast, PLC/InsP3/Ca2+ functions to regulate metabolic adaptability and gene transcription. Autophagy is a catabolic process involved in protein degradation, organelle turnover, and nonselective breakdown of cytoplasmic components during nutrient starvation or stress. In the heart, autophagy is observed in a variety of human pathologies, where it can be either adaptive or maladaptive, depending on the context. We proposed the hypothesis that IGF-1 protects the heart by rescuing the mitochondrial metabolism and the energetics state, reducing cell death and controls the potentially exacerbate autophagic response to nutritional stress. In light of the importance of IGF-1 and autophagy in the heart, we review here IGF-1 signaling and autophagy regulation in the context of cardiomyocyte nutritional stress.

Original languageEnglish (US)
Pages (from-to)593-601
Number of pages9
JournalIUBMB Life
Volume65
Issue number7
DOIs
StatePublished - Jul 2013

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Autophagy
Somatomedins
Extracellular Signal-Regulated MAP Kinases
Type C Phospholipases
Sirolimus
Cardiac Myocytes
Inositol 1,4,5-Trisphosphate
Cell growth
Pathology
Cell death
Transcription
Growth
Starvation
Metabolism
Organelles
Protein Kinases
Nutrients
Proteolysis
Cell Survival
Cell Death

Keywords

  • general bioenergetics
  • signal transduction
  • signaling

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Clinical Biochemistry
  • Molecular Biology
  • Genetics

Cite this

Troncoso, R., Díaz-Elizondo, J., Espinoza, S. P., Navarro-Marquez, M. F., Oyarzún, A. P., Riquelme, J. A., ... Lavandero, S. (2013). Regulation of cardiac autophagy by insulin-like growth factor 1. IUBMB Life, 65(7), 593-601. https://doi.org/10.1002/iub.1172

Regulation of cardiac autophagy by insulin-like growth factor 1. / Troncoso, Rodrigo; Díaz-Elizondo, Jessica; Espinoza, Sandra P.; Navarro-Marquez, Mario F.; Oyarzún, Alejandra P.; Riquelme, Jaime A.; Garcia-Carvajal, Ivonne; Díaz-Araya, Guillermo; García, Lorena; Hill, Joseph A; Lavandero, Sergio.

In: IUBMB Life, Vol. 65, No. 7, 07.2013, p. 593-601.

Research output: Contribution to journalArticle

Troncoso, R, Díaz-Elizondo, J, Espinoza, SP, Navarro-Marquez, MF, Oyarzún, AP, Riquelme, JA, Garcia-Carvajal, I, Díaz-Araya, G, García, L, Hill, JA & Lavandero, S 2013, 'Regulation of cardiac autophagy by insulin-like growth factor 1', IUBMB Life, vol. 65, no. 7, pp. 593-601. https://doi.org/10.1002/iub.1172
Troncoso R, Díaz-Elizondo J, Espinoza SP, Navarro-Marquez MF, Oyarzún AP, Riquelme JA et al. Regulation of cardiac autophagy by insulin-like growth factor 1. IUBMB Life. 2013 Jul;65(7):593-601. https://doi.org/10.1002/iub.1172
Troncoso, Rodrigo ; Díaz-Elizondo, Jessica ; Espinoza, Sandra P. ; Navarro-Marquez, Mario F. ; Oyarzún, Alejandra P. ; Riquelme, Jaime A. ; Garcia-Carvajal, Ivonne ; Díaz-Araya, Guillermo ; García, Lorena ; Hill, Joseph A ; Lavandero, Sergio. / Regulation of cardiac autophagy by insulin-like growth factor 1. In: IUBMB Life. 2013 ; Vol. 65, No. 7. pp. 593-601.
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