Huang Weiyi, Liu Xinghui, Chen Rong, Feng Liqiang, Liao Hua, Yu Lei, Zeng Huijun
Department of Human Anatomy, Southern Medical University, the Key Laboratory of Construction and Detection of Guangdong Province, Guangzhou Guangdong, 510515, P.R.China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2012 Jun;26(6):735-42.
To explore the effects of mechanical stretch with variant frequencies on the alignment and differentiation of the multilayer myotubes cultured in vitro, and to select the optimized cultural condition of regenerative skeletal muscle tissue with stress loading cultured in vitro.
C2C12 myoblasts cultured in vitro in the groove casts of Sylgard 184 were induced into the multilayer myotubes. Meanwhile the myoblasts were treated with various mechanical stretch with cells tensile instrument, at the amplitude of 10% and the frequency of 0 (group A), 0.25 (group B), 0.50 (group C), and 1.00 Hz (group D) for 1 hour, 3 times a day. The myotubes morphology was observed by inverted phase contrast microscope at 5, 7, and 10 days after continuous mechanical stretch. And the expressions of mRNA for myogenic differentiation antigen (MyoD), Myogenin, Desmin, and myosin heavy chain (MyHC) were detected by RT-PCR and real-time fluorescent quantitative PCR (QRT-PCR), respectively.
The mechanical stretch could promote the aligned fusion and increase the number of myotubes. Indeed the multilayer myotubes arranged more closely in group B at 7 days. At the same group, as the time went on, the mRNA expressions of MyoD gradually declined in each group. There were significant differences in mRNA expressions of MyoD between 5 days and 7, 10 days (P < 0.05). The mRNA expressions of Myogenin, Desmin, and MyHC were highest at 7 days. There were significant differences between different time points (P < 0.05), except the mRNA expression of Desmin of group B between 7 and 10 days (P > 0.05). At the same time, with the increase of frequency, the highest mRNA expressions of MyoD, Myogenin, Desmin, and MyHC were in group B. There were significant differences at the same time between group B and the other groups (P < 0.05), except mRNA expression of Desmin at 5 days between groups B and C, and mRNA expression of MyHC at 10 days between groups A and B (P > 0.05).
Low frequency (0.25 Hz) and suitable time (7 days) periodic mechanical stretch is beneficial to the differentiation of the multilayer myotubes cultured in the groove casts of Sylgard 184, but as the stretch time goes on the aging of myotubes will be accelerated.
探讨不同频率的机械牵张对体外培养的多层肌管排列及分化的影响,筛选体外应力加载培养再生骨骼肌组织的优化培养条件。
将体外培养于Sylgard 184凹槽铸型中的C2C12成肌细胞诱导形成多层肌管。同时,使用细胞拉伸仪对成肌细胞进行不同频率的机械牵张,牵张幅度为10%,频率分别为0(A组)、0.25(B组)、0.50(C组)和1.00 Hz(D组),每天3次,每次1小时。连续机械牵张后第5、7和10天,用倒置相差显微镜观察肌管形态。分别采用RT-PCR和实时荧光定量PCR(QRT-PCR)检测生肌分化抗原(MyoD)、生肌调节因子、结蛋白和肌球蛋白重链(MyHC)的mRNA表达。
机械牵张可促进肌管排列融合并增加肌管数量。实际上,B组在第7天时多层肌管排列更紧密。在同一组中,随着时间推移,各组MyoD的mRNA表达逐渐下降。MyoD的mRNA表达在第5天与第7、10天之间存在显著差异(P < 0.05)。生肌调节因子、结蛋白和MyHC的mRNA表达在第7天时最高。不同时间点之间存在显著差异(P < 0.05),B组结蛋白在第7天和第10天的mRNA表达除外(P > 0.05)。同时,随着频率增加,MyoD、生肌调节因子、结蛋白和MyHC的mRNA最高表达均在B组。B组与其他组在同一时间存在显著差异(P < 0.05),B组和C组在第5天结蛋白的mRNA表达以及A组和B组在第10天MyHC的mRNA表达除外(P > 0.05)。
低频(0.25 Hz)和适宜时间(7天)的周期性机械牵张有利于体外培养于Sylgard 184凹槽铸型中的多层肌管分化,但随着牵张时间延长,肌管会加速老化。