Kim Junghwan, Won Kyung-Jong, Jung Seung Hyo, Lee Kang-Pa, Shim Sun Bo, Kim Mee-Young, Kim Ju-Hyun, Lee Jeong-Uk, Kim Bokyung
Department of Physical Therapy, College of Public Health & Welfare, Yongin University, Yongin-city 449-714, South Korea.
Department of Medicine, Konkuk University School of Medicine, Chungju-city 380-701, South Korea.
Life Sci. 2015 Dec 15;143:50-7. doi: 10.1016/j.lfs.2015.09.016. Epub 2015 Sep 25.
The purpose of this study is to explore whether antioxidant DJ-1 protein affects the atrophy of skeletal muscle cell induced by undernutrition.
To determine cell atrophic responses, L6 cell line and skeletal primary cells from mouse hind limbs were cultivated under condition of FBS-free and low glucose. Changes of protein expression were analyzed using Western blot. Overexpression and knockdown of DJ-1 was performed in cells to assess its influence on cell atrophic responses.
Undernutrition decreased cell size and increased the abundance of oxidized form and total form of DJ-1 protein in L6 myoblasts. The undernourished cells revealed an elevation in the expression of muscle-specific RING finger-1 (MuRF-1) and atrogin-1, and in the phosphorylations of p38 mitogen-activated protein kinase (MAPK) and stress-activated protein kinase/c-Jun N-terminal kinase compared with control groups. Moreover, DJ-1-knockout mice showed a decrease in cell size and an enhancement in the expression of MuRF-1 and atrogin-1, as well as in the phosphorylation of MAPKs in gastrocnemius muscles; these changes were also observed in L6 cells transfected with siRNA of DJ-1. On the other hand, L6 cells overexpressing full-length DJ-1 did not exhibit the alterations in cell size and ubiquitin ligases seen after undernourished states of control cells. Myotubes differentiated from L6 cells also showed elevated expression of MuRF-1 and atrogin-1 in response to undernutrition.
These results suggest that DJ-1 protein may contribute to undernutrition-induced atrophy via MAPKs/ubiquitin ligase pathway in skeletal muscle cells.
本研究旨在探讨抗氧化剂DJ-1蛋白是否影响营养不足诱导的骨骼肌细胞萎缩。
为了确定细胞萎缩反应,将L6细胞系和来自小鼠后肢的骨骼肌原代细胞在无胎牛血清和低糖条件下培养。使用蛋白质印迹法分析蛋白质表达的变化。在细胞中进行DJ-1的过表达和敲低,以评估其对细胞萎缩反应的影响。
营养不足会减小L6成肌细胞的细胞大小,并增加DJ-1蛋白氧化形式和总形式的丰度。与对照组相比,营养不足的细胞显示肌肉特异性E3泛素连接酶1(MuRF-1)和肌肉萎缩相关蛋白1(atrogin-1)的表达升高,以及p38丝裂原活化蛋白激酶(MAPK)和应激激活蛋白激酶/c-Jun氨基末端激酶的磷酸化增加。此外,DJ-1基因敲除小鼠的腓肠肌细胞大小减小,MuRF-1和atrogin-1的表达增强,以及MAPKs的磷酸化增加;在转染了DJ-1小干扰RNA的L6细胞中也观察到了这些变化。另一方面,过表达全长DJ-1的L6细胞在对照细胞营养不足状态后未表现出细胞大小和泛素连接酶的改变。从L6细胞分化而来的肌管在营养不足时也显示出MuRF-1和atrogin-1的表达升高。
这些结果表明,DJ-1蛋白可能通过MAPKs/泛素连接酶途径在骨骼肌细胞中促成营养不足诱导的萎缩。