4.3 Review

Analysis of CaM-kinase signaling in cells

期刊

CELL CALCIUM
卷 50, 期 1, 页码 1-8

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.ceca.2011.02.007

关键词

Calcium; CaM kinase; CaM kinase I; CaM kinase kinase; CaM kinase IV; CaM kinase II, neuron; Dominant negative, sh-RNA

资金

  1. NIH [MH086032, NS027037, GM041292]
  2. Hope for Depression Foundation
  3. Ministry of Education, Culture, Sports, Science and Technology of Japan [21570143]
  4. Grants-in-Aid for Scientific Research [21570143] Funding Source: KAKEN

向作者/读者索取更多资源

A change in intracellular free calcium is a common signaling mechanism that modulates a wide array of physiological processes in most cells. Responses to increased intracellular Ca(2+) are often mediated by the ubiquitous protein calmodulin (CaM) that upon binding Ca(2+) can interact with and alter the functionality of numerous proteins including a family of protein kinases referred to as CaM-kinases (CaMKs). Of particular interest are multifunctional CaMKs, such as CaMKI, CaMKII, CaMKIV and CaMKK, that can phosphorylate multiple downstream targets. This review will outline several protocols we have used to identify which members and/or isoforms of this CaMK family mediate specific cellular responses with a focus on studies in neurons. Many previous studies have relied on a single approach such as pharmacological inhibitors or transfected dominant-negative kinase constructs. Since each of these protocols has its limitations, that will be discussed, we emphasize the necessity to use multiple, independent approaches in mapping out cellular signaling pathways. Published by Elsevier Ltd.

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