Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/45304
Título: The phospholipase C-InsP(3) pathway is involved in calcium mobilization induced by growth hormone in hepatocytes
Autores/as: Marrero Arencibia, María Isabel 
Déniz, A.
Clasificación UNESCO: 32 Ciencias médicas
320102 Genética clínica
2415 Biología molecular
Palabras clave: Isolated Rat Hepatocytes
C-Dependent Processes
Polymorphonuclear Neutrophils
Inositol 1,4,5-Trisphosphate
Signal-Transduction, et al.
Fecha de publicación: 2004
Publicación seriada: Growth Hormone and IGF Research 
Resumen: We investigated the effects of bovine GH (bGH) on Ca2+ handling, phospholipase C (PLC) activation and inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] formation in hepatocytes. bGH generates oscillations in cytosolic free Ca2+ concentration ([Ca2+]i) in single male rat hepatocytes microinjected with the photoprotein aequorin. In the absence of extracellular Ca2+ these transients persisted for more than 10 min indicating a requirement for intracellular Ca2+. Treatment of the hepatocyte with the phosphatidylinositol-specific phospholipase C (PI-PLC) inhibitor U-73122 removed the oscillations. These results suggest bGH-induced oscillations are due to PLC activation and generation of Ins(1,4,5)P3. We measured the mass of Ins(1,4,5)P3 in freshly isolated hepatocyte suspensions in response to bGH, and vasopressin as a control. Both agonists rapidly increased the levels of Ins(1,4,5)P3. This is the first study to indicate that early events in the signal transduction pathways mediated by GH in hepatocytes involve intracellular Ca2+ mobilization via activation of a PI-PLC and subsequent Ins(1,4,5 )P3 production.
URI: http://hdl.handle.net/10553/45304
ISSN: 1096-6374
DOI: 10.1016/j.ghir.2003.11.001
Fuente: Growth Hormone & Igf Research [ISSN 1096-6374],v. 14 (2), p. 85-90
Colección:Artículos
Vista completa

Google ScholarTM

Verifica

Altmetric


Comparte



Exporta metadatos



Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.