IIB   20738
INSTITUTO DE INVESTIGACIONES BIOLOGICAS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
ACTIVATED AMPK IS CRUCIAL TO ACHIEVING RESILIENT HYPOMETABOLIC STATE DURING DORMANCY IN THE ECHINOCOCCUS GRANULOSUS LARVAL STAGES.
Autor/es:
JULIA LOOS; DANIELA VILLAMONTE; ANDREA CUMINO
Lugar:
Mar del Plata
Reunión:
Congreso; LVIII Reunión Anual de la Sociedad Argentina de Investigación Clínica (SAIC); 2013
Institución organizadora:
LVIII Reunión Científica Anual de la Sociedad Argentina de Investigación Clínica (SAIC), Reunión Anual de la Sociedad Argentina de Fisiología (SAFIS), XLV Reunión Anual de la Sociedad Argentina de Farmaco
Resumen:
Molecular pathways which are activated to induce the hypometabolism include stimulation of the AMP-activated protein kinase (AMPK) in nematodes and insects. The inverse relationship between TOR and AMPK activity is critical for long term survival when nutrients are limiting. It is unknown in *Echinococcus granulosus *larval stages, causative agent of the human hydatidosis. Previously, we identified and analyzed encoding genes for α, β and γ subunits of Eg-AMPK and carried out transcriptional expression studies of these prototypical subunits in the parasite. Furthermore, we demonstrated that an AMPK agonist, the metformin, reduced the vitality of protoscoleces and metacestodes in a dose-dependent manner; decreased the transcriptional expression level of *pepck*, *g6p* and *mdh*, increased the type II fermentation and induced autophagy, indicating that a prolonged exposure to the drug impairs the energy asset of larval stages. In this work, we showed that metformin effects resulted in a mitochondrial membrane depolarization as shown by JC-1 stain, indicating a raise in the AMP levels and the allosteric activation of AMPK. Also, AMPK was highly activated in control protoscoleces and was confirmed its sensibility to metformin by two-fold increases in the amount of active phosphorylated AMPK (Eg-AMPKα-PThr176) assessed by immunoblotting. The phosphorylation of Eg-AMPKα implicates upstream kinases, LKB1 and CaMKK, both identified by their conserved structures in the cestode. Additionally, we identified highly conserved C-terminal hydrophobic amino acids that function as a nuclear export sequence (NES) in the AMPKα and its nuclear expression in control protoscoleces by confocal microscopy was verified. Due to the recent description of FoxO proteins as transcriptional regulators targeted by AMPK linked with signaling during hypometabolism states, we identified the only one FoxO ortholog in *E. granulosus* genome in accordance to the occurrence in others invertebrates.