首页> 美国卫生研究院文献>The Korean Journal of Physiology Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology >p38 MAPK Participates in Muscle-Specific RING Finger 1-Mediated Atrophy in Cast-Immobilized Rat Gastrocnemius Muscle
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p38 MAPK Participates in Muscle-Specific RING Finger 1-Mediated Atrophy in Cast-Immobilized Rat Gastrocnemius Muscle

机译:p38 MAPK参与固定肌源性大鼠腓肠肌的肌肉特异性RING指1介导的萎缩。

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摘要

Skeletal muscle atrophy is a common phenomenon during the prolonged muscle disuse caused by cast immobilization, extended aging states, bed rest, space flight, or other factors. However, the cellular mechanisms of the atrophic process are poorly understood. In this study, we investigated the involvement of mitogen-activated protein kinase (MAPK) in the expression of muscle-specific RING finger 1 (MuRF1) during atrophy of the rat gastrocnemius muscle. Histological analysis revealed that cast immobilization induced the atrophy of the gastrocnemius muscle, with diminution of muscle weight and cross-sectional area after 14 days. Cast immobilization significantly elevated the expression of MuRF1 and the phosphorylation of p38 MAPK. The starvation of L6 rat skeletal myoblasts under serum-free conditions induced the phosphorylation of p38 MAPK and the characteristics typical of cast-immobilized gastrocnemius muscle. The expression of MuRF1 was also elevated in serum-starved L6 myoblasts, but was significantly attenuated by SB203580, an inhibitor of p38 MAPK. Changes in the sizes of L6 myoblasts in response to starvation were also reversed by their transfection with MuRF1 small interfering RNA or treatment with SB203580. From these results, we suggest that the expression of MuRF1 in cast-immobilized atrophy is regulated by p38 MAPK in rat gastrocnemius muscles.
机译:骨骼肌萎缩是在因石膏固定,老化状态延长,卧床休息,太空飞行或其他因素引起的肌肉长期停用期间的常见现象。然而,对萎缩过程的细胞机制了解甚少。在这项研究中,我们调查了大鼠腓肠肌萎缩过程中有丝分裂原活化蛋白激酶(MAPK)参与肌肉特异性RING手指1(MuRF1)的表达。组织学分析表明,石膏固定导致腓肠肌萎缩,14天后肌肉重量和横截面积减小。铸模固定化显着提高了MuRF1的表达和p38 MAPK的磷酸化。 L6大鼠骨骼肌成肌细胞在无血清条件下的饥饿诱导了p38 MAPK的磷酸化和铸型固定腓肠肌的典型特征。在血清饥饿的L6成肌细胞中,MuRF1的表达也升高,但被p38 MAPK抑制剂SB203580显着减弱。 L6成肌细胞响应饥饿的大小变化也可以通过用MuRF1小干扰RNA转染或用SB203580处理而逆转。从这些结果,我们表明,在大鼠腓肠肌中,p38 MAPK调节了铸模固定性萎缩中MuRF1的表达。

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