
doi: 10.1038/nn952
pmid: 12368808
We used differential screening of cDNAs from individual taste receptor cells to identify candidate taste transduction elements in mice. Among the differentially expressed clones, one encoded Trpm5, a member of the mammalian family of transient receptor potential (TRP) channels. We found Trpm5 to be expressed in a restricted manner, with particularly high levels in taste tissue. In taste cells, Trpm5 was coexpressed with taste-signaling molecules such as alpha-gustducin, Ggamma13, phospholipase C-beta2 (PLC-beta2) and inositol 1,4,5-trisphosphate receptor type III (IP3R3). Our heterologous expression studies of Trpm5 indicate that it functions as a cationic channel that is gated when internal calcium stores are depleted. Trpm5 may be responsible for capacitative calcium entry in taste receptor cells that respond to bitter and/or sweet compounds.
Medical Sciences, Medical Physiology, Phospholipase C beta, Gene Expression, Receptors, Cytoplasmic and Nuclear, TRPM Cation Channels, CHO Cells, Mice, Cricetinae, Medicine and Health Sciences, Cell Biology & Physiology, Animals, Inositol 1,4,5-Trisphosphate Receptors, RNA, Messenger, Transducin, Cloning, Molecular, Neurosciences, Membrane Proteins, Taste Buds, Medical Cell Biology, Isoenzymes, Medical Neurobiology, Taste, Type C Phospholipases, Oocytes, Calcium, Calcium Channels, Physiological Processes, Neuroscience
Medical Sciences, Medical Physiology, Phospholipase C beta, Gene Expression, Receptors, Cytoplasmic and Nuclear, TRPM Cation Channels, CHO Cells, Mice, Cricetinae, Medicine and Health Sciences, Cell Biology & Physiology, Animals, Inositol 1,4,5-Trisphosphate Receptors, RNA, Messenger, Transducin, Cloning, Molecular, Neurosciences, Membrane Proteins, Taste Buds, Medical Cell Biology, Isoenzymes, Medical Neurobiology, Taste, Type C Phospholipases, Oocytes, Calcium, Calcium Channels, Physiological Processes, Neuroscience
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