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AMP-activated protein kinase (AMPK) is the downstream component of a protein kinase cascade that plays a key role in the regulation of energy metabolism. In humans, mutations in the gamma2-subunit of AMPK cause cardiac hypertrophy associated with Wolff-Parkinson-White syndrome, characterized by ventricular preexcitation. The effect of these mutations on AMPK activity and in development of the disease is enigmatic. Here we report that transgenic mice with cardiac-specific expression of gamma2 harboring a mutation of arginine residue 531 to glycine (RG-TG) develop a striking cardiac phenotype by 4 wk of age, including hypertrophy, impaired contractile function, electrical conduction abnormalities, and marked glycogen accumulation. At this stage, AMPK activity isolated from hearts of RG-TG mice was almost completely abolished but could be restored after phosphorylation by an upstream AMPK kinase. At 1 wk of age, there was no detectable evidence of a cardiac phenotype, and AMPK activity in RG-TG hearts was similar to that in nontransgenic, control mice. We propose that mutations in gamma2 lead to suppression of total cardiac AMPK activity secondary to increased glycogen accumulation. The subsequent decrease in AMPK activity provides a mechanism that may explain the development of cardiac hypertrophy in this model.

Original publication

DOI

10.1152/ajpheart.01020.2005

Type

Journal article

Journal

Am J Physiol Heart Circ Physiol

Publication Date

05/2006

Volume

290

Pages

H1942 - H1951

Keywords

AMP-Activated Protein Kinases, Animals, Cardiomegaly, Disease Models, Animal, Female, Humans, Mice, Mice, Transgenic, Multienzyme Complexes, Mutagenesis, Site-Directed, Mutation, Protein-Serine-Threonine Kinases, Structure-Activity Relationship, Wolff-Parkinson-White Syndrome