TRPV1-lineage neurons are required for thermal sensation

被引:212
作者
Mishra, Santosh K. [1 ]
Tisel, Sarah M. [1 ]
Orestes, Peihan [1 ]
Bhangoo, Sonia K. [1 ]
Hoon, Mark A. [1 ]
机构
[1] NIDCR, Mol Genet Unit, Lab Sensory Biol, NIH, Bethesda, MD 20892 USA
关键词
itch; pain; thermal; TRPM8; TRPV1; MAMMALIAN TASTE RECEPTORS; CAPSAICIN-RECEPTOR; MICE LACKING; IN-VIVO; BEHAVIORAL-RESPONSES; NEUROPATHIC PAIN; TRP CHANNEL; COLD; THERMOSENSATION; ACTIVATION;
D O I
10.1038/emboj.2010.325
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ion-channel TRPV1 is believed to be a major sensor of noxious heat, but surprisingly animals lacking TRPV1 still display marked responses to elevated temperature. In this study, we explored the role of TRPV1-expressing neurons in somatosensation by generating mice wherein this lineage of cells was selectively labelled or ablated. Our data show that TRPV1 is an embryonic marker of many nociceptors including all TRPV1- and TRPM8-neurons as well as many Mrg-expressing neurons. Mutant mice lacking these cells are completely insensitive to hot or cold but in marked contrast retain normal touch and mechanical pain sensation. These animals also exhibit defective body temperature control and lose both itch and pain reactions to potent chemical mediators. Together with previous cell ablation studies, our results define and delimit the roles of TRPV1- and TRPM8-neurons in thermosensation, thermoregulation and nociception, thus significantly extending the concept of labelled lines in somatosensory coding. The EMBO Journal (2011) 30, 582-593. doi:10.1038/emboj.2010.325; Published online 7 December 2010
引用
收藏
页码:582 / 593
页数:12
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