Mammalian Trp Channels As Molecular Targets

Transient receptor potential (TRP) genes were originally identified as encoding critical components of phototransduction in Drosophila. Since the discovery of the first mammalian transient receptor potential channel (TRPC), more than 20 mammalian homologues have been reported. These ion channel proteins are widely distributed in tissues and appear to play a fundamental role in cell signalling, growth and death. There are two major subfamilies of TRP channels. The TRPV channels include the VR1 vanilloid receptor, epithelial Ca2+ channels and OTRPC4, a channel that appears to be regulated by changes in osmolarity. Their functions may range from sensory transduction in nerves to Ca2+ transport in the gastrointestinal tract and renal tubule. The TRPM channels, which are the largest proteins in the TRP family, include the founding member, melastatin, and a novel bifunctional channel enzyme, TRP-PLIK. This book brings together contributions from key investigators in the area of TRP channels. It covers the structure, function and regulation of mammalian TRP channels and of mechanisms of signal transduction. The discussions highlight future studies towards a better understanding of the role of TRP channels in normal cellular physiology, the involvement of TRP channels in disease states, and their potential use as molecular targets for novel therapeutic agents. Related Novartis Foundation symposia: 245 Ion channels: from atomic resolution physiology to functional genomics Chair: Frances Ashcroft 241 Sodium channels and neuronal hyperexcitability Chair: Stephen G. WaxmanNovartis Foundation Symposium Staff is the author of 'Mammalian Trp Channels As Molecular Targets' with ISBN 9780470862544 and ISBN 0470862548.