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在培养的成年大鼠骨骼肌纤维中,钠离子通道 Na(V)1.5 的表达增强。

Sodium channel Na(V)1.5 expression is enhanced in cultured adult rat skeletal muscle fibers.

机构信息

Université de Bretagne Occidentale, Brest, France.

出版信息

J Membr Biol. 2010 Jun;235(2):109-19. doi: 10.1007/s00232-010-9262-5. Epub 2010 Jun 2.

Abstract

This study analyzes changes in the distribution, electrophysiological properties, and proteic composition of voltage-gated sodium channels (Na(V)) in cultured adult rat skeletal muscle fibers. Patch clamp and molecular biology techniques were carried out in flexor digitorum brevis (FDB) adult rat skeletal muscle fibers maintained in vitro after cell dissociation with collagenase. After 4 days of culture, an increase of the Na(V)1.5 channel type was observed. This was confirmed by an increase in TTX-resistant channels and by Western blot test. These channels exhibited increased activation time constant (tau(m)) and reduced conductance, similar to what has been observed in denervated muscles in vivo, where the density of Na(V)1.5 was increasing progressively after denervation. By real-time polymerase chain reaction, we found that the expression of beta subunits was also modified, but only after 7 days of culture: increase in beta(1) without beta(4) modifications. beta(1) subunit is known to induce a negative shift of the inactivation curve, thus reducing current amplitude and duration. At day 7, tau(h) was back to normal and tau(m) still increased, in agreement with a decrease in sodium current and conductance at day 4 and normalization at day 7. Our model is a useful tool to study the effects of denervation in adult muscle fibers in vitro and the expression of sodium channels. Our data evidenced an increase in Na(V)1.5 channels and the involvement of beta subunits in the regulation of sodium current and fiber excitability.

摘要

本研究分析了培养的成年大鼠骨骼肌纤维中电压门控钠离子通道(Na(V))的分布、电生理特性和蛋白组成的变化。在体外细胞解离后用胶原酶培养的屈趾短肌(FDB)成年大鼠骨骼肌纤维中进行了膜片钳和分子生物学技术。在培养的第 4 天,观察到 Na(V)1.5 通道类型增加。TTX 抗性通道的增加和 Western blot 测试证实了这一点。这些通道表现出激活时间常数(tau(m))增加和电导降低,类似于体内去神经肌肉中观察到的情况,其中去神经后 Na(V)1.5 的密度逐渐增加。通过实时聚合酶链反应,我们发现β亚基的表达也发生了改变,但仅在培养的第 7 天:β1 增加而β4 不变。β1 亚基已知会引起失活曲线的负移,从而降低电流幅度和持续时间。在第 7 天,tau(h)恢复正常,tau(m)仍在增加,这与第 4 天钠电流和电导的减少以及第 7 天的正常化一致。我们的模型是研究体外成年肌纤维去神经作用和钠离子通道表达的有用工具。我们的数据表明 Na(V)1.5 通道增加,β亚基参与调节钠电流和纤维兴奋性。

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