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
. 2006;100(5):519-24.
doi: 10.1254/jphs.cpj06004x. Epub 2006 May 13.

Calcium ion as a second messenger with special reference to excitation-contraction coupling

Affiliations
Free article
Review

Calcium ion as a second messenger with special reference to excitation-contraction coupling

Makoto Endo. J Pharmacol Sci. 2006.
Free article

Abstract

Calcium ion (Ca(2+)) plays an important role in stimulus-response reactions of cells as a second messenger. This is done by keeping cytoplasmic Ca(2+) concentration low at rest and by mobilizing Ca(2+) in response to stimulus, which in turn activates the cellular reaction. The role of Ca(2+) as a second messenger was first discovered in excitation-contraction coupling of skeletal muscle. The history of the discovery was reviewed. Characteristics of Ca(2+) as a second messenger, diversity of target molecules, capability of rapid and massive mobilization and also of oscillatory mobilization, tendency toward localization, and on the other side, ability to cause generalized cell response were described. The possible bases for these characteristics was discussed. Ca(2+) itself induces release of Ca(2+) from the sarcoplasmic reticulum (Ca(2+)-induced Ca(2+) release [CICR]). The Ca(2+) release channel, ryanodine receptor, incorporated into lipid bilayer shows CICR activity. Ca(2+) release induced by inositol trisphosphate also has an apparent CICR nature. The significance of CICR or apparent CICR with its inherently regenerative nature in physiological contractions of skeletal, cardiac, and smooth muscles was discussed.

PubMed Disclaimer

MeSH terms

Substances