Conte Elena, Fonzino Adriano, Cibelli Antonio, De Benedictis Vito, Imbrici Paola, Nicchia Grazia Paola, Pierno Sabata, Camerino Giulia Maria
Department of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Bari, Italy.
Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari "Aldo Moro", Bari, Italy.
Front Pharmacol. 2020 May 15;11:714. doi: 10.3389/fphar.2020.00714. eCollection 2020.
The ClC-1 chloride channel 1 is important for muscle function as it stabilizes resting membrane potential and helps to repolarize the membrane after action potentials. We investigated the contribution of ClC-1 to adaptation of skeletal muscles to needs induced by the different stages of life. We analyzed the ClC-1 gene and protein expression as well as mRNA levels of protein kinase C (PKC) alpha and theta involved in ClC-1 modulation, in soleus (SOL) and extensor digitorum longus (EDL) muscles of rats in all stage of life. The cellular localization of ClC-1 in relation to age was also investigated. Our data show that during muscle development ClC-1 expression differs according to phenotype. In fast-twitch EDL muscles ClC-1 expression increased 10-fold starting at 7 days up to 8 months of life. Conversely, in slow-twitch SOL muscles ClC-1 expression remained constant until 33 days of life and subsequently increased fivefold to reach the adult value. Aging induced a downregulation of gene and protein ClC-1 expression in both muscle types analyzed. The mRNA of PKC-theta revealed the same trend as ClC-1 except in old age, whereas the mRNA of PKC-alpha increased only after 2 months of age. Also, we found that the ClC-1 is localized in both membrane and cytoplasm, in fibers of 12-day-old rats, becoming perfectly localized on the membrane in 2-month-old rats. This study could represent a point of comparison helpful for the identification of accurate pharmacological strategies for all the pathological situations in which ClC-1 protein is altered.
氯离子通道蛋白1(ClC-1)对肌肉功能很重要,因为它能稳定静息膜电位,并在动作电位后帮助使膜复极化。我们研究了ClC-1在骨骼肌适应生命不同阶段所产生需求过程中的作用。我们分析了ClC-1基因和蛋白表达,以及参与ClC-1调节的蛋白激酶C(PKC)α和θ的mRNA水平,这些分析针对的是处于生命各阶段大鼠的比目鱼肌(SOL)和趾长伸肌(EDL)。我们还研究了ClC-1与年龄相关的细胞定位情况。我们的数据表明,在肌肉发育过程中,ClC-1的表达因表型而异。在快肌型EDL肌肉中,从出生7天到8个月,ClC-1的表达增加了10倍。相反,在慢肌型SOL肌肉中,ClC-1的表达在出生33天前保持恒定,随后增加了5倍,达到成年水平。衰老导致所分析的两种肌肉类型中ClC-1的基因和蛋白表达下调。PKC-θ的mRNA显示出与ClC-1相同的趋势,除了在老年阶段,而PKC-α的mRNA仅在2个月龄后增加。此外,我们发现,在12日龄大鼠的纤维中,ClC-1定位于细胞膜和细胞质中,而在2月龄大鼠中则完全定位于细胞膜上。这项研究可以作为一个比较点,有助于为所有ClC-1蛋白发生改变的病理情况确定准确的药理学策略。