Lee Hyo Gun, Choi Jae-Young, Park Jung-Woong, Park Tae Sub, Song Ki-Duk, Shin Donghyun, Cho Byung-Wook
Department of Animal Science, College of Natural Resources and Life Sciences, Pusan National University, Miryang 50463, Korea.
Graduate School of International Agricultural Technology and Institute of Green-Bio Science and Technology, Seoul National University, Pyeongchang 25354, Korea.
Asian-Australas J Anim Sci. 2019 Mar;32(3):350-356. doi: 10.5713/ajas.18.0375. Epub 2018 Sep 13.
To examine the regulatory effects of exercise on myokine expression in horse skeletal muscle cells, we compared the expression of several myokine genes (interleukin 6 [IL-6], IL-8, chemokine [C-X-C motif] ligand 2 [CXCL2], and chemokine [C-C motif] ligand 4 [CCL4]) after a single bout of exercise in horses. Furthermore, to establish in vitro systems for the validation of exercise effects, we cultured horse skeletal muscle cells and confirmed the expression of these genes after treatment with hydrogen peroxide.
The mRNA expression of IL-6, IL-8, CXCL2, and CCL4 after exercise in skeletal muscle tissue was confirmed using quantitative-reverse transcriptase polymerase chain reactions (qRT-PCR). We then extracted horse muscle cells from the skeletal muscle tissue of a neonatal Thoroughbred. Myokine expression after hydrogen peroxide treatments was confirmed using qRT-PCR in horse skeletal muscle cells.
IL-6, IL-8, CXCL2, and CCL4 expression in Thoroughbred and Jeju horse skeletal muscles significantly increased after exercise. We stably maintained horse skeletal muscle cells in culture and confirmed the expression of the myogenic marker, myoblast determination protein (MyoD). Moreover, myokine expression was validated using hydrogen peroxide (H2O2)-treated horse skeletal muscle cells. The patterns of myokine expression in muscle cells were found to be similar to those observed in skeletal muscle tissue.
We confirmed that several myokines involved in inflammation were induced by exercise in horse skeletal muscle tissue. In addition, we successfully cultured horse skeletal muscle cells and established an in vitro system to validate associated gene expression and function. This study will provide a valuable system for studying the function of exercise-related genes in the future.
为了研究运动对马骨骼肌细胞中肌动蛋白表达的调节作用,我们比较了马单次运动后几种肌动蛋白基因(白细胞介素6 [IL-6]、IL-8、趋化因子[C-X-C基序]配体2 [CXCL2]和趋化因子[C-C基序]配体4 [CCL4])的表达。此外,为了建立用于验证运动效果的体外系统,我们培养了马骨骼肌细胞,并在用过氧化氢处理后确认了这些基因的表达。
使用定量逆转录聚合酶链反应(qRT-PCR)确认运动后骨骼肌组织中IL-6、IL-8、CXCL2和CCL4的mRNA表达。然后我们从一匹新生纯种马的骨骼肌组织中提取马肌肉细胞。使用qRT-PCR在马骨骼肌细胞中确认过氧化氢处理后的肌动蛋白表达。
纯种马和济州马骨骼肌中IL-6、IL-8、CXCL2和CCL4的表达在运动后显著增加。我们在培养中稳定维持马骨骼肌细胞,并确认了生肌标志物成肌细胞决定蛋白(MyoD)的表达。此外,使用过氧化氢(H2O2)处理的马骨骼肌细胞验证了肌动蛋白的表达。发现肌肉细胞中肌动蛋白的表达模式与骨骼肌组织中观察到的相似。
我们证实,马骨骼肌组织中的运动诱导了几种参与炎症的肌动蛋白。此外,我们成功培养了马骨骼肌细胞,并建立了一个体外系统来验证相关基因的表达和功能。这项研究将为未来研究运动相关基因的功能提供一个有价值的系统。