Induced Chondrogenic Differentiation of hESCs by hESC-Derived MSCs Conditioned Medium and Sequential 3D-2D Culture System

Shayesteh Shahriary, Ehsan Farashahi-Yazd, Fatemeh Hajizadeh-Tafti, F. Akyash, B. Aflatoonian
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Abstract

Background and Aims: It has been proven that human mesenchymal stem cells (MSCs) conditioned medium (hMSCs-CM) can influence human embryonic stem cells (hESCs) chondrogenic differentiation. In this study, we hypothesized that conditioned medium (CM) from hESCs-derived MSCs in a sequential 3D-2D culture system could facilitate the induction of chondrogenesis in hESCs. Materials and Methods: CM was collected from Yazd2 (hESCs; 46, XY) derived MSCs confluent cultures and stored at -20 °C. Yazd4 hESC line (46, XX) was induced for differentiation using EB formation as 3D culture into SD (spontaneously differentiation) and CM groups (differentiation using conditioned medium) for four days. Cell culture continued in a 2D (monolayer) culture system for both groups till day 14. Ultimately, chondrogenic differentiation was assessed by Alcian blue and masson′s trichrome staining at 4 and 14 days of differentiation, and quantitative real-time polymerase chain reaction (PCR) for NANOG, MEOX1, SOX5, SOX6, SOX9, ACAN, COL2A1 and RUNX2 genes for SD and CM groups on days 0 and 4. Results: The gene expression profile for chondrogenic genes in the CM group was significantly more than the SD group (p< 0.05). Furthermore, chemical staining assessment illustrated a significant GAG and collagen II difference between the CM and SD groups at days 4 and 14 (p< 0.05). Conclusions: Our findings would pave the way for creating an in vitro human chondrogenesis model for further studies in the developmental biology of articular cartilage tissue, which lend itself to cell-based therapy to cure joint diseases such as osteoarthritis.
hesc来源的MSCs条件培养基和顺序3D-2D培养系统诱导hesc成软骨分化
背景与目的:人间充质干细胞(MSCs)条件培养基(hMSCs-CM)可以影响人胚胎干细胞(hESCs)的软骨分化。在这项研究中,我们假设从hESCs衍生的MSCs中提取的条件培养基(CM)在连续的3D-2D培养系统中可以促进hESCs的软骨形成。材料和方法:从Yazd2 (hESCs)中收集CM;46, XY)衍生的MSCs融合培养并保存在-20°C。将Yazd4 hESC系(46,XX)以EB胚为3D培养物诱导分化为SD组(自发分化)和CM组(条件培养基分化),培养4 d。两组细胞继续在二维(单层)培养系统中培养至第14天。最终,在分化第4天和第14天,采用阿利新蓝和马松三色染色法评估软骨分化,并在第0天和第4天对SD组和CM组的NANOG、MEOX1、SOX5、SOX6、SOX9、ACAN、COL2A1和RUNX2基因进行实时定量聚合酶链反应(PCR)。结果:CM组软骨形成基因表达谱显著高于SD组(p< 0.05)。此外,化学染色评估显示,CM组和SD组在第4天和第14天的GAG和II型胶原蛋白差异显著(p< 0.05)。结论:我们的发现将为创建体外人类软骨形成模型铺平道路,为进一步研究关节软骨组织的发育生物学奠定基础,使其成为细胞治疗骨关节炎等关节疾病的基础。
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