Differential expression of TRPV1 and TRPM8 in the mouse trigeminal ganglion and spinal dorsal root ganglion.

IF 2 4区 医学 Q3 NEUROSCIENCES
Caifeng Shao, Jichao Wei, Hong-Yi Jia, Yu-Han Zhou, Mingwei Zhao, Kun Yang, Ming-Ming Zhang
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引用次数: 0

Abstract

Transient receptor potential (TRP) ion channels, including the thermoreceptor TRP vanilloid 1 (TRPV1) and innocuous warm detector TRP melastatin 8 (TRPM8), are widely expressed on the primary sensory neurons of the trigeminal ganglion (TG) and the dorsal root ganglion (DRG). By performing real-time quantitative PCR and immunostaining, we compared TRPV1 and TRPM8 gene expression and immunostaining in mouse DRG and TG neurons. Both TRPV1 and TRPM8 are widely expressed in the TG and DRG, but in different patterns: TRPV1 has relatively more abundant expression and immunostaining in the DRG, whereas TRPM8 has higher levels in the TG. Double-staining for TRPV1 and TRPM8 revealed very little coexpression in either the TG or the DRG. These results suggest that TRPV1 and TRPM8 are differentially expressed in TG and DRG, and this significant variation may underlie the different temperature sensory properties of the skin and oral cavity.

TRPV1和TRPM8在小鼠三叉神经节和脊髓背根神经节中的差异表达。
瞬时受体电位(TRP)离子通道在三叉神经节(TG)和背根神经节(DRG)的初级感觉神经元上广泛表达,包括热感受器TRP vanilloid 1 (TRPV1)和无害的热感受器TRP melastatin 8 (TRPM8)。通过实时定量PCR和免疫染色,我们比较了TRPV1和TRPM8基因在小鼠DRG和TG神经元中的表达和免疫染色。TRPV1和TRPM8均在TG和DRG中广泛表达,但表达模式不同:TRPV1在DRG中表达和免疫染色相对更丰富,而TRPM8在TG中表达水平更高。TRPV1和TRPM8的双染色在TG和DRG中均很少共表达。这些结果表明,TRPV1和TRPM8在TG和DRG中的表达存在差异,这种显著的差异可能是皮肤和口腔不同温度感觉特性的基础。
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来源期刊
Neuroscience Letters
Neuroscience Letters 医学-神经科学
CiteScore
5.20
自引率
0.00%
发文量
408
审稿时长
50 days
期刊介绍: Neuroscience Letters is devoted to the rapid publication of short, high-quality papers of interest to the broad community of neuroscientists. Only papers which will make a significant addition to the literature in the field will be published. Papers in all areas of neuroscience - molecular, cellular, developmental, systems, behavioral and cognitive, as well as computational - will be considered for publication. Submission of laboratory investigations that shed light on disease mechanisms is encouraged. Special Issues, edited by Guest Editors to cover new and rapidly-moving areas, will include invited mini-reviews. Occasional mini-reviews in especially timely areas will be considered for publication, without invitation, outside of Special Issues; these un-solicited mini-reviews can be submitted without invitation but must be of very high quality. Clinical studies will also be published if they provide new information about organization or actions of the nervous system, or provide new insights into the neurobiology of disease. NSL does not publish case reports.
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