Regulation of cell cycle progression by calcium/calmodulin-dependent pathways.

Published

Journal Article (Review)

Many hormones, growth factors, and cytokines regulate proliferation of their target cells. Perhaps the most universal signaling cascades required for proliferative responses are those initiated by transient rises in intracellular calcium (Ca(2+)). The major intracellular receptor for Ca(2+) is calmodulin (CaM). CaM is a small protein that contains four EF-hand Ca(2+) binding sites and is highly conserved among eukaryotes. In all organisms in which the CaM gene has been deleted, it is essential. Although Ca(2+)/CaM is required for proliferation in both unicellular and multicellular eukaryotes, the essential targets of Ca(2+)/CaM-dependent pathways required for cell proliferation remain elusive. Potential Ca(2+)/CaM-dependent targets include the serine/threonine phosphatase calcineurin and the family of multifunctional Ca(2+)/CaM-dependent protein kinases. Whereas these enzymes are essential in Aspergillus nidulans, they are not required under normal growth conditions in yeast. However, in mammalian cells, studies demonstrate that both types of enzymes contribute to the regulation of cell cycle progression. Unfortunately, the mechanism by which Ca(2+)/CaM and its downstream targets, particularly calcineurin and the Ca(2+)/CaM-dependent protein kinases, regulate key cell cycle-regulatory proteins, remains enigmatic. By understanding how Ca(2+)/CaM regulates cell cycle progression in normal mammalian cells, we may gain insight into how hormones control cell division and how cancer cells subvert the need for Ca(2+) and its downstream targets to proliferate.

Full Text

Duke Authors

Cited Authors

  • Kahl, CR; Means, AR

Published Date

  • December 2003

Published In

Volume / Issue

  • 24 / 6

Start / End Page

  • 719 - 736

PubMed ID

  • 14671000

Pubmed Central ID

  • 14671000

Electronic International Standard Serial Number (EISSN)

  • 1945-7189

International Standard Serial Number (ISSN)

  • 0163-769X

Digital Object Identifier (DOI)

  • 10.1210/er.2003-0008

Language

  • eng