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AKAP-Lbc Mobilizes a Cardiac Hypertrophy Signaling Pathway

  • Graeme K. Carnegie
  • , 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

Research output: Contribution to journalArticlepeer-review

120 Scopus citations

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.

Original languageEnglish
Pages (from-to)169-179
Number of pages11
JournalMolecular Cell
Volume32
Issue number2
DOIs
StatePublished - Oct 24 2008

Keywords

  • HUMDISEASE
  • SIGNALING

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