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大鼠骨骼肌ClC-1氯通道的表达及细胞定位变化与年龄、肌纤维表型和蛋白激酶C调节的关系

Changes in Expression and Cellular Localization of Rat Skeletal Muscle ClC-1 Chloride Channel in Relation to Age, Myofiber Phenotype and PKC Modulation.

作者信息

Conte Elena, Fonzino Adriano, Cibelli Antonio, De Benedictis Vito, Imbrici Paola, Nicchia Grazia Paola, Pierno Sabata, Camerino Giulia Maria

机构信息

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.

出版信息

Front Pharmacol. 2020 May 15;11:714. doi: 10.3389/fphar.2020.00714. eCollection 2020.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a82b/7243361/006b9c1cd009/fphar-11-00714-g002.jpg

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