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Sodium-calcium exchanger and multiple sodium channel isoforms in intra-epidermal nerve terminals

机译:表皮内神经末梢中的钠钙交换剂和多种钠通道亚型

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Background Nociception requires transduction and impulse electrogenesis in nerve fibers which innervate the body surface, including the skin. However, the molecular substrates for transduction and action potential initiation in nociceptors are incompletely understood. In this study, we examined the expression and distribution of Na+/Ca2+ exchanger (NCX) and voltage-gated sodium channel isoforms in intra-epidermal free nerve terminals. Results Small diameter DRG neurons exhibited robust NCX2, but not NCX1 or NCX3 immunolabeling, and virtually all PGP 9.5-positive intra-epidermal free nerve terminals displayed NCX2 immunoreactivity. Sodium channel NaV1.1 was not detectable in free nerve endings. In contrast, the majority of nerve terminals displayed detectable levels of expression of NaV1.6, NaV1.7, NaV1.8 and NaV1.9. Sodium channel immunoreactivity in the free nerve endings extended from the dermal boundary to the terminal tip. A similar pattern of NCX and sodium channel immunolabeling was observed in DRG neurons in vitro. Conclusions NCX2, as well as NaV1.6, NaV1.7, NaV1.8 and NaV1.9, are present in most intra-epidermal free nerve endings. The presence of NCX2, together with multiple sodium channel isoforms, in free nerve endings may have important functional implications.
机译:背景技术伤害感受需要神经纤维的传导和脉冲电产生,神经纤维支配身体表面,包括皮肤。但是,对于伤害感受器中的转导和动作电位引发的分子底物尚未完全了解。在这项研究中,我们检查了Na + / Ca2 +交换子(NCX)和电压门控钠通道亚型在表皮内游离神经末梢的表达和分布。结果小直径DRG神经元表现出强健的NCX2,但没有NCX1或NCX3免疫标记,并且实际上所有PGP 9.5阳性表皮内游离神经末梢均显示NCX2免疫反应性。游离神经末梢中未检测到钠通道NaV1.1。相反,大多数神经末梢显示出可检测到的NaV1.6,NaV1.7,NaV1.8和NaV1.9表达水平。游离神经末梢中的钠通道免疫反应性从真皮边界延伸至末端。在体外DRG神经元中观察到了类似的NCX和钠通道免疫标记模式。结论NCX2以及NaV1.6,NaV1.7,NaV1.8和NaV1.9存在于大多数表皮内游离神经末梢。游离神经末梢中NCX2的存在以及多种钠通道亚型可能具有重要的功能意义。

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