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http://dx.doi.org/10.5483/BMBRep.2013.46.5.077

SERCA2a: a prime target for modulation of cardiac contractility during heart failure

Park, Woo Jin (Global Research Laboratory and College of Life Sciences, Gwangju Institute of Science and Technology)
Oh, Jae Gyun (Global Research Laboratory and College of Life Sciences, Gwangju Institute of Science and Technology)

Publication Information

BMB Reports / v.46, no.5, 2013 , pp. 237-243 More about this Journal

Abstract

Heart failure is one of the leading causes of sudden death in developed countries. While current therapies are mostly aimed at mitigating associated symptoms, novel therapies targeting the subcellular mechanisms underlying heart failure are emerging. Failing hearts are characterized by reduced contractile properties caused by impaired $Ca^{2+}$ cycling between the sarcoplasm and sarcoplasmic reticulum (SR). Sarcoplasmic/endoplasmic reticulum $Ca^{2+}$ ATPase 2a (SERCA2a) mediates $Ca^{2+}$ reuptake into the SR in cardiomyocytes. Of note, the expression level and/or activity of SERCA2a, translating to the quantity of SR $Ca^{2+}$ uptake, are significantly reduced in failing hearts. Normalization of the SERCA2a expression level by gene delivery has been shown to restore hampered cardiac functions and ameliorate associated symptoms in pre-clinical as well as clinical studies. SERCA2a activity can be regulated at multiple levels of a signaling cascade comprised of phospholamban, protein phosphatase 1, inhibitor-1, and $PKC{\alpha}$ . SERCA2 activity is also regulated by post-translational modifications including SUMOylation and acetylation. In this review, we will highlight the molecular mechanisms underlying the regulation of SERCA2a activity and the potential therapeutic modalities for the treatment of heart failure.

Keywords

Inhibitor-1; Phospholamban; $PKC{\alpha}$ ; Protein phosphatase 1; SERCA2a;

Citations & Related Records

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