Hwang Jeongmi, Lee Sang-Jin, Yoo Miran, Go Ga-Yeon, Lee Da Yeon, Kim Yong-Kee, Seo Dong-Wan, Kang Jong-Sun, Ryu Jae-Ha, Bae Gyu-Un
Research Center for Cell Fate Control, College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Republic of Korea.
College of Pharmacy, Dankook University, Cheonan 330-714, Republic of Korea.
Biochem Biophys Res Commun. 2015 Jan 2;456(1):471-5. doi: 10.1016/j.bbrc.2014.11.109. Epub 2014 Dec 5.
The activation of MyoD family transcription factors is critical for myogenic differentiation, which is fundamental to the regeneration of skeletal muscle after injury. Kazinol-P (KP) from Broussonetia kazinoki (B. kazinoki), a natural compound, has been reported to possess an anti-oxidant function. In a screen of natural compounds for agonists of the MyoD activity, we identified KP and examined its effect on myoblast differentiation. Consistently, KP enhanced the myotube formation, accompanied with upregulation of myogenic markers such as MHC, Myogenin and Troponin-T. KP treatment in C2C12 myoblasts led to strong activation of a key promyogenic kinase p38MAPK in a dose, and time-dependent manner. Furthermore, KP treatment enhanced the MyoD-mediated trans-differentiation of 10T1/2 fibroblasts into myoblasts. Taken together, KP promotes myogenic differentiation through activation of p38MAPK and MyoD transcription activities. Thus KP may be a potential therapeutic candidate to prevent fibrosis and improve muscle regeneration and repair.
肌分化蛋白(MyoD)家族转录因子的激活对于肌源性分化至关重要,而肌源性分化是损伤后骨骼肌再生的基础。来自构树(Broussonetia kazinoki)的天然化合物卡齐诺醇-P(Kazinol-P,KP)已被报道具有抗氧化功能。在筛选天然化合物作为MyoD活性激动剂的过程中,我们鉴定出了KP,并研究了其对成肌细胞分化的影响。一致的是,KP增强了肌管的形成,并伴随着肌源性标志物如肌球蛋白重链(MHC)、肌细胞生成素(Myogenin)和肌钙蛋白-T(Troponin-T)的上调。在C2C12成肌细胞中进行KP处理,以剂量和时间依赖性方式导致关键的促肌源性激酶p38丝裂原活化蛋白激酶(p38MAPK)强烈激活。此外,KP处理增强了MyoD介导的10T1/2成纤维细胞向成肌细胞的转分化。综上所述,KP通过激活p38MAPK和MyoD转录活性促进肌源性分化。因此,KP可能是预防纤维化以及改善肌肉再生和修复的潜在治疗候选物。