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J Physiol Volume 582, Number 3, 939-944, August 1, 2007 DOI: 10.1113/jphysiol.2007.132522
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SYMPOSIUM REPORTS

Modulation of TRPs by PIPs

Thomas Voets1 and Bernd Nilius1

1 Laboratory of Ion Channel Research, Division of Physiology, Department of Molecular Cell Biology, KU Leuven, Onderwijs & Navorsing 1, Herestraat 49 bus 802, 3000 Leuven, Belgium

The TRP superfamily of cation channels encompasses 28 mammalian members related to the product of the Drosophila trp (transient receptor potential) gene. TRP channels have a widespread distribution in many cell types and organs and gate in response to a broad variety of physical and chemical stimuli; as such, they can be considered as ubiquitous cellular sensors. Several recent studies reported modulation of different TRP channels by phosphoinositides, in particular by phosphatidylinositol 4,5-bisphosphate (PIP2). In most cases, PIP2 promotes TRP channel activation. Here we provide a brief overview of current insights and controversies about the mechanisms and structural determinants of PIP2–TRP channel interactions, and zoom in on the regulation of the Ca2+- and voltage-gated TRPM4 by phosphoinositides.

(Received 15 March 2007; accepted after revision 27 March 2007; first published online 29 March 2007)
Corresponding author T. Voets: Laboratory of Ion Channel Research, Division of Physiology, Department of Molecular Cell Biology, KU Leuven, Onderwijs & Navorsing 1, Herestraat 49 bus 802, 3000 Leuven, Belgium. Email: thomas.voets{at}med.kuleuven.be


This report was presented at The Journal of Physiology Symposium on Regulation of ion channels and transporters by phosphatidylinositol 4,5-bisphosphate (PIP2), Baltimore, MD, USA, 2 March 2007. It was commissioned by the Editorial Board and reflects the views of the authors.




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