Oki K, Yoshihara S, Urushihata N, Ghazizadeh M
Research & Development Division, BioMimetics Sympathies Inc., Koto-ku, Tokyo, Japan.
Eur Rev Med Pharmacol Sci. 2021 Aug;25(15):4953-4963. doi: 10.26355/eurrev_202108_26452.
Recent investigations have demonstrated that the administration of MSC in mouse model of diseases provided beneficial effects. On the other hand, human adipose-derived MSC condition medium (ADSC-CM) is reported as containing beneficial secreted factors, but its role in muscle fibrosis has not been identified. The aim of this study was to investigate the inhibitory effects of MSC-CM in muscle fibrosis in vitro using the C2C12 murine muscle, myoblast cell line.
C2C12 cells were cultured overnight in 0.1% albumin-Dulbecco's Modifies Eagle's Medium (DMEM). The cells were then pre-incubated in ADSC-CM for 20 min, treated with 2.5-10 ng/mL human TGFβ1 for 8-72 hours and analyzed using RT-qPCR, Western blot and immunofluorescent staining.
Treatment with 20% ADSC-CM for 3 days suppressed αSMA protein expression in TGFβ1 treated C2C12 cells. ADSC-CM stimulated the proliferation of C2C12 cells in a dose-dependent manner. Furthermore, TGFβ1 induced Acta2/αSMA mRNA expression which was inhibited by ADSC-CM treatment for 8 hours. Decorin, one of the dermatan sulfate proteoglycans and an endogenous inhibitor of TGFβ1, was expressed in ADSC-CM, but not in TGFβ1 pre-incubated ADSC-CM.
Our studies provide useful information for establishing anti-fibrotic mechanism(s) of ADSC-CM, thus facilitating potential application to prevent muscle fibrosis.
近期研究表明,在疾病小鼠模型中给予间充质干细胞(MSC)具有有益效果。另一方面,据报道人脂肪来源的间充质干细胞条件培养基(ADSC-CM)含有有益的分泌因子,但其在肌肉纤维化中的作用尚未明确。本研究旨在使用C2C12小鼠肌肉成肌细胞系在体外研究MSC-CM对肌肉纤维化的抑制作用。
将C2C12细胞在含0.1%白蛋白的杜尔贝科改良伊格尔培养基(DMEM)中培养过夜。然后将细胞在ADSC-CM中预孵育20分钟,用2.5 - 10 ng/mL人转化生长因子β1(TGFβ1)处理8 - 72小时,并通过实时定量聚合酶链反应(RT-qPCR)、蛋白质免疫印迹法(Western blot)和免疫荧光染色进行分析。
用20%的ADSC-CM处理3天可抑制TGFβ1处理的C2C12细胞中α平滑肌肌动蛋白(αSMA)蛋白的表达。ADSC-CM以剂量依赖的方式刺激C2C12细胞的增殖。此外,TGFβ1诱导的α平滑肌肌动蛋白(Acta2/αSMA)信使核糖核酸(mRNA)表达在ADSC-CM处理8小时后受到抑制。核心蛋白聚糖是硫酸皮肤素蛋白聚糖之一,也是TGFβ1的内源性抑制剂,在ADSC-CM中表达,但在预先用TGFβ1孵育的ADSC-CM中不表达。
我们的研究为确立ADSC-CM的抗纤维化机制提供了有用信息,从而有助于其在预防肌肉纤维化方面的潜在应用。