1. Academic Validation
  2. AKAP-Lbc mobilizes a cardiac hypertrophy signaling pathway

AKAP-Lbc mobilizes a cardiac hypertrophy signaling pathway

  • Mol Cell. 2008 Oct 24;32(2):169-79. doi: 10.1016/j.molcel.2008.08.030.
Graeme K Carnegie 1 Joseph Soughayer F Donelson Smith Benjamin S Pedroja Fang Zhang Dario Diviani Michael R Bristow Maya T Kunkel Alexandra C Newton Lorene K Langeberg John D Scott
Affiliations

Affiliation

  • 1 Howard Hughes Medical Institute, Vollum Institute, Oregon Health and Science University, Portland, OR 97239, USA.
Abstract

Elevated catecholamines in the heart evoke transcriptional activation of the Myocyte Enhancer Factor (MEF) pathway to induce a cellular response known as pathological myocardial hypertrophy. We have discovered that the A-Kinase Anchoring Protein (AKAP)-Lbc is upregulated in hypertrophic cardiomyocytes. It coordinates activation and movement of signaling proteins that initiate MEF2-mediated transcriptional reprogramming events. Live-cell imaging, fluorescent kinase activity reporters, and RNA interference techniques show that AKAP-Lbc couples activation of protein kinase D (PKD) with the phosphorylation-dependent nuclear export of the class II histone deacetylase HDAC5. These studies uncover a role for AKAP-Lbc in which increased expression of the anchoring protein selectively amplifies a signaling pathway that drives cardiac myocytes toward a pathophysiological outcome.

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