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PMID: 15530641 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

The TRPM ion channel subfamily: molecular, biophysical and functional features.

Trends in pharmacological sciences ·Vol. 25 ·No. 12 ·2004-12-00 ·Pages 633-9

Fleig A, Penner R

Abstract

Significant progress in the molecular and functional characterization of a subfamily of genes that encode melastatin-related transient receptor potential (TRPM) cation channels has been made during the past few years. This subgroup of the TRP superfamily of ion channels contains eight mammalian members and has isoforms in most eukaryotic organisms. The individual members of the TRPM subfamily have specific expression patterns and ion selectivity, and their specific gating and regulatory mechanisms are tailored to integrate multiple signaling pathways. The diverse functional properties of these channels have a profound effect on the regulation of ion homoeostasis by mediating direct influx of Ca2+, controlling Mg2+ entry, and determining the potential of the cell membrane. TRPM channels are involved in several physiological and pathological conditions in electrically excitable and non-excitable cells, which make them exciting targets for drug discovery.

MeSH Terms
Animals Calcium/metabolism Calcium Channels/genetics,physiology Cell Membrane/metabolism Humans Ion Channels/genetics,physiology Magnesium/metabolism Signal Transduction
Chemicals
Calcium Channels Ion Channels Magnesium Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fleig Andrea
Laboratory of Cell and Molecular Signaling, Center for Biomedical Research, The Queen's Medical Center and Department of Cell and Molecular Biology, John A. Burns School of Medicine, The University of Hawaii, Honolulu, HI 96813, USA.
Penner Reinhold
Article Info
Journal
Trends in pharmacological sciences
Abbr.
Trends Pharmacol Sci
ISSN
0165-6147
Published
2004-12-00
Pages
633-9
Language
English
Region
England
NLM ID
7906158
Subset
IM
Grants
NIGMS NIH HHS · R01-GM065360 · United States
NIGMS NIH HHS · R01-GM63954 · United States
NINDS NIH HHS · R01-NS040927 · United States
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