Piezo1 通道在大鼠足底肌肉机械合成代谢耦合中的作用

IF 1.1 Q4 CELL BIOLOGY
K. V. Sergeeva, S. A. Tyganov, V. E. Kalashnikov, B. S. Shenkman, T. M. Mirzoev
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引用次数: 0

摘要

摘要 众所周知,肌肉纤维在机械应力作用下的蛋白质合成激活和肥大是通过依赖于 mTORC1 的同化信号途径实现的。然而,能够感知机械信号并将其进一步传递给依赖于 mTORC1 的信号途径(机械传导)的机械传感器却鲜为人知。机械激活(MA)离子通道是此类肌浆机械传感器的候选角色。因此,本研究的目的是调查 MA 通道(Piezo1)在离体大鼠比目鱼肌对机械应力的反应中激活 mTORC1 依赖性通路的潜在作用。将 Wistar 大鼠分为 3 组:(1) "对照组"(动物肌肉不接触 MA 通道抑制剂或 Piezo1 通道激活剂);(2) "钆组"(动物肌肉与氯化钆、MA 通道抑制剂一起孵育);(3) "尤达组"(动物肌肉与尤达 1、Piezo1 MA 通道激活剂一起孵育)。各组大鼠的比目鱼肌均从左侧肢体分离出来,在相应溶液中培养,不施加一系列拉伸形式的机械应力("静止");右侧肢体的比目鱼肌接受一系列拉伸("拉伸"),然后在相应溶液中培养。通过 PAAG 电泳和免疫印迹测定大鼠比目鱼肌中 mTORC1 靶标(p70S6K、rpS6 和 4E-BP1)的磷酸化。与未承受机械应力的肌肉相比,离体比目鱼肌的一系列被动拉伸导致 p70S6K、其底物 rpS6 和 4E-BP1 的磷酸化分别增加了 38.5%、168% 和 112%。用钆培养肌肉完全阻止了一系列拉伸引起的 mTORC1 标记的激活。与未接触 Yoda1 的肌肉相比,将比目鱼肌置于含有 Yoda1 的溶液中会导致 p70S6K、rpS6 和 4E-BP1 的机械依赖性磷酸化减少。因此,这项研究采用的方法并未揭示 Piezo1 参与了大鼠比目鱼肌的机械-合成代谢耦合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Role of Piezo1 Channels in Mechano-Anabolic Coupling in Rat Soleus Muscle

Role of Piezo1 Channels in Mechano-Anabolic Coupling in Rat Soleus Muscle

Role of Piezo1 Channels in Mechano-Anabolic Coupling in Rat Soleus Muscle

It is known that activation of protein synthesis and hypertrophy of muscle fibers in response to mechanical stress is realized through an anabolic mTORC1-dependent signaling pathway. However, mechanosensors through which a mechanical signal can be perceived and further transmitted to the mTORC1-dependent signaling pathway (mechanotransduction) are poorly identified. Mechanically activated (MA) ion channels are candidates for the role of such sarcolemmal mechanosensors. In this regard, the aim of this study was to investigate the potential role of MA channels (Piezo1) in the activation of the mTORC1-dependent pathway in the isolated rat soleus muscle in response to mechanical stress. Wistar rats were divided into 3 groups: (1) “Control” (animal muscles were not exposed to MA channel inhibitor or Piezo1 channel activator); (2) “Gadolinium” (animal muscles were incubated with gadolinium chloride, MA channel inhibitor), and (3) “Yoda” (animal muscles were incubated with Yoda1, Piezo1 MA channel activator). In rats from each group, m. soleus was isolated from the left limb and incubated in the appropriate solution without mechanical stress in the form of a series of stretching (“Rest”); m. soleus from the right limb was subjected to a series of stretching (“Stretch”) and then incubated in the appropriate solution. Phosphorylation of mTORC1 targets (p70S6K, rpS6, and 4E-BP1) in rat m. soleus was determined by PAAG electrophoresis and immunoblotting. A series of passive stretches of isolated m. soleus led to an increase in the phosphorylation of p70S6K, its substrate rpS6, and 4E-BP1 by 38.5, 168 and 112%, respectively, compared to the muscle that was not subjected to mechanical stress. Incubation of the muscles with gadolinium completely prevented the activation of mTORC1 markers caused by a series of stretches. Incubation of m. soleus in a solution with Yoda1 resulted in a decrease in the mechano-dependent phosphorylation of p70S6K, rpS6 and 4E-BP1 compared to the muscle that was not exposed to Yoda1. Thus, the methodological approach used in this work did not reveal the participation of Piezo1 in mechano-anabolic coupling in rat m. soleus.

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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
28
期刊介绍: Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology   is an international peer reviewed journal that publishes original articles on physical, chemical, and molecular mechanisms that underlie basic properties of biological membranes and mediate membrane-related cellular functions. The primary topics of the journal are membrane structure, mechanisms of membrane transport, bioenergetics and photobiology, intracellular signaling as well as membrane aspects of cell biology, immunology, and medicine. The journal is multidisciplinary and gives preference to those articles that employ a variety of experimental approaches, basically in biophysics but also in biochemistry, cytology, and molecular biology. The journal publishes articles that strive for unveiling membrane and cellular functions through innovative theoretical models and computer simulations.
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