Cell-specific alternative splicing increases calcium channel current density in the pain pathway

被引:172
作者
Bell, TJ [1 ]
Thaler, C [1 ]
Castiglioni, AJ [1 ]
Helton, TD [1 ]
Lipscombe, D [1 ]
机构
[1] Brown Univ, Dept Neurosci, Providence, RI 02912 USA
关键词
D O I
10.1016/S0896-6273(03)00801-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
N-type calcium channels are critical for pain transduction. Inhibitors of these channels are powerful analgesics, but clinical use of current N-type blockers; remains limited by undesirable actions in other regions of the nervous system. We now demonstrate that a unique splice isoform of the N-type channel is restricted exclusively to dorsal root ganglia. By a combination of functional and molecular analyses at the single-cell level, we show that the DRG-specific exon, e37a, is preferentially present in Ca(V)2.2 mRNAs expressed in neurons that contain nociceptive markers, VR1 and Na(V)1.8. Cell-specific inclusion of exon 37a correlates closely with significantly larger N-type currents in nociceptive neurons. This unique splice isoform of the N-type channel could represent a novel target for pain management.
引用
收藏
页码:127 / 138
页数:12
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