International Union of Basic and Clinical Pharmacology. LXXVI. Current Progress in the Mammalian TRP Ion Channel Family

被引:436
作者
Wu, Long-Jun
Sweet, Tara-Beth
Clapham, David E. [1 ]
机构
[1] Childrens Hosp Boston, Howard Hughes Med Inst, Dept Cardiol, Manton Ctr Orphan Dis, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
EPITHELIAL CA2+ CHANNEL; POLYCYSTIC KIDNEY-DISEASE; MUCOLIPIDOSIS TYPE-IV; NONSELECTIVE CATION CHANNEL; RECEPTOR POTENTIAL CHANNEL; PROTEIN-KINASE-C; VARITINT-WADDLER PHENOTYPE; INTEGRAL MEMBRANE-PROTEIN; ACTIVATED CALCIUM-CHANNEL; CELL TRANSDUCTION CHANNEL;
D O I
10.1124/pr.110.002725
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Transient receptor potential (TRP) channels are a large family of ion channel proteins, surpassed in number in mammals only by voltage-gated potassium channels. TRP channels are activated and regulated through strikingly diverse mechanisms, making them suitable candidates for cellular sensors. They respond to environmental stimuli such as temperature, pH, osmolarity, pheromones, taste, and plant compounds, and intracellular stimuli such as Ca2+ and phosphatidylinositol signal transduction pathways. However, it is still largely unknown how TRP channels are activated in vivo. Despite the uncertainties, emerging evidence using TRP channel knockout mice indicates that these channels have broad function in physiology. Here we review the recent progress on the physiology, pharmacology and pathophysiological function of mammalian TRP channels.
引用
收藏
页码:381 / 404
页数:24
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