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      Junctophilin-2 expression silencing causes cardiocyte hypertrophy and abnormal intracellular calcium-handling.

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          Abstract

          Junctophilin-2 (JPH2), a protein expressed in the junctional membrane complex, is necessary for proper intracellular calcium (Ca(2+)) signaling in cardiac myocytes. Downregulation of JPH2 expression in a model of cardiac hypertrophy was recently associated with defective coupling between plasmalemmal L-type Ca(2+) channels and sarcoplasmic reticular ryanodine receptors. However, it remains unclear whether JPH2 expression is altered in patients with hypertrophic cardiomyopathy (HCM). In addition, the effects of downregulation of JPH2 expression on intracellular Ca(2+) handling are presently poorly understood. We sought to determine whether loss of JPH2 expression is noted among patients with HCM and whether expression silencing might perturb Ca(2+) handling in a prohypertrophic manner.

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          Author and article information

          Journal
          Circ Heart Fail
          Circulation. Heart failure
          1941-3297
          1941-3289
          Mar 2011
          : 4
          : 2
          Affiliations
          [1 ] Department of Molecular Pharmacology & Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN 55905, USA.
          Article
          CIRCHEARTFAILURE.110.958694 NIHMS271398
          10.1161/CIRCHEARTFAILURE.110.958694
          3059380
          21216834
          6c8cb125-c533-4aed-97bb-7b1f3ad47a4c
          History

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