Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2005 Dec;37(6):375-80.
doi: 10.1007/s10863-005-9474-z.

SERCA2a in heart failure: role and therapeutic prospects

Affiliations
Review

SERCA2a in heart failure: role and therapeutic prospects

Davide Gianni et al. J Bioenerg Biomembr. 2005 Dec.

Abstract

Ca(2+) is a key molecule controlling several cellular processes, from fertilization to cell death, in all cell types. In excitable and contracting cells, such as cardiac myocytes, Ca(2+) controls muscle contractility. The spatial and temporal segregation of Ca(2+) concentrations are central to maintain its concentration gradients across the cells and the cellular compartments for proper function. SERCA2a is a cornerstone molecule for maintaining a balanced concentration of Ca(2+) during the cardiac cycle, since it controls the transport of Ca(2+) to the sarcoplasmic reticulum (SR) during relaxation. Alterations of the activity of this pump have been widely investigated, emphasizing its central role in the control of Ca(2+) homeostasis and consequently in the pathogenesis of the contractile defect seen with heart failure. This review focuses on the molecular characteristics of the pump, its role during the cardiac cycle and the prospects derived from the manipulation of SERCA2a for heart failure treatment.

PubMed Disclaimer

References

    1. J Biol Chem. 1989 Aug 5;264(22):13038-42 - PubMed
    1. Circulation. 1990 Oct;82(4):1266-78 - PubMed
    1. Circ Res. 2001 Mar 2;88(4):415-21 - PubMed
    1. Trends Cardiovasc Med. 2003 May;13(4):152-7 - PubMed
    1. J Biol Chem. 1991 Oct 5;266(28):18839-45 - PubMed

MeSH terms

Substances