Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Cytoplasmic Ca(2+) is an universal intracellular messenger that activates cellular responses over a broad temporal range, from neurotransmitter release to cell growth and proliferation. Inherent to the use of the multifarious Ca(2+) signal is the question of specificity: how can some Ca(2+)-dependent responses be activated in a cell and not others? A rise in cytoplasmic Ca(2+) can evoke a response either by binding directly to the target (as occurs with certain Ca(2+)-activated K(+) and Cl(-) channels, for example) or through recruitment of intermediary proteins, such as calmodulin and troponin C. A substantial body of evidence has now established that Ca(2+)-binding proteins differ both in their affinities for Ca(2+) and in their on- and off-rates for Ca(2+) binding/unbinding. Furthermore, different Ca(2+)-binding proteins often occupy distinct locations within the cell. Therefore, the size, kinetics and spatial profile of a cytoplasmic Ca(2+) signal are all important in determining which Ca(2+)-dependent response will be activated, when and for how long.

Original publication

DOI

10.4161/chan.25298

Type

Journal article

Journal

Channels (Austin)

Publication Date

09/2013

Volume

7

Pages

374 - 378

Keywords

NFAT, calcium signaling, gene expression, store-operated channels, transcription factor, Animals, Calcium Channels, Calcium Signaling, Cell Adhesion Molecules, Gene Expression Regulation, Humans, Membrane Proteins, Neoplasm Proteins, ORAI1 Protein, Stromal Interaction Molecule 1, Stromal Interaction Molecule 2