AKAP-Lbc Mobilizes a Cardiac Hypertrophy Signaling Pathway

被引:116
|
作者
Carnegie, Graeme K. [1 ,5 ]
Soughayer, Joseph [1 ,5 ]
Smith, F. Donelson [1 ,5 ]
Pedroja, Benjamin S. [1 ,5 ]
Zhang, Fang [1 ,5 ]
Diviani, Dario [2 ]
Bristow, Michael R. [3 ]
Kunkel, Maya T. [4 ]
Newton, Alexandra C. [4 ]
Langeberg, Lorene K. [1 ,5 ]
Scott, John D. [1 ,5 ]
机构
[1] Univ Washington, Howard Hughes Med Inst, Dept Pharmacol, Sch Med, Seattle, WA 98195 USA
[2] Univ Lausanne, Dept Pharmacol & Toxicol, CH-1005 Lausanne, Switzerland
[3] Univ Colorado, Hlth Sci Ctr, Div Cardiol, Denver, CO 80262 USA
[4] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[5] Oregon Hlth & Sci Univ, Vollum Inst, Howard Hughes Med Inst, Portland, OR 97239 USA
关键词
D O I
10.1016/j.molcel.2008.08.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:169 / 179
页数:11
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