Hamidi Sofiane, Letourneur Didier, Aid-Launais Rachida, Di Stefano Antonio, Vainchenker William, Norol Françoise, Le Visage Catherine
1 INSERM, UMR 1009, Institut Gustave Roussy , Villejuif, France .
Tissue Eng Part A. 2014 Apr;20(7-8):1285-94. doi: 10.1089/ten.TEA.2013.0149. Epub 2014 Feb 14.
Somatic stem cells require specific niches and three-dimensional scaffolds provide ways to mimic this microenvironment. Here, we studied a scaffold based on Fucoidan, a sulfated polysaccharide known to influence morphogen gradients during embryonic development, to support human embryonic stem cells (hESCs) differentiation toward the cardiac lineage. A macroporous (pore 200 μm) Fucoidan scaffold was selected to support hESCs attachment and proliferation. Using a protocol based on the cardiogenic morphogen bone morphogenic protein 2 (BMP2) and transforming growth factor (TGFβ) followed by tumor necrosis factor (TNFα), an effector of cardiopoietic priming, we examined the cardiac differentiation in the scaffold compared to culture dishes and embryoid bodies (EBs). At day 8, Fucoidan scaffolds supported a significantly higher expression of the 3 genes encoding for transcription factors marking the early step of embryonic cardiac differentiation NKX2.5 (p<0.05), MEF2C (p<0.01), and GATA4 (p<0.01), confirmed by flow cytometry analysis for MEF2C and NKX2.5. The ability of Fucoidan scaffolds to locally concentrate and slowly release TGFβ and TNFα was confirmed by Luminex technology. We also found that Fucoidan scaffolds supported the late stage of embryonic cardiac differentiation marked by a significantly higher atrial natriuretic factor (ANF) expression (p<0.001), although only rare beating areas were observed. We postulated that absence of mechanical stress in the soft hydrogel impaired sarcomere formation, as confirmed by molecular analysis of the cardiac muscle myosin MYH6 and immunohistological staining of sarcomeric α-actinin. Nevertheless, Fucoidan scaffolds contributed to the development of thin filaments connecting beating areas through promotion of smooth muscle cells, thus enabling maintenance of beating areas for up to 6 months. In conclusion, Fucoidan scaffolds appear as a very promising biomaterial to control cardiac differentiation from hESCs that could be further combined with mechanical stress to promote sarcomere formation at terminal stages of differentiation.
体细胞干细胞需要特定的微环境,而三维支架提供了模拟这种微环境的方法。在此,我们研究了一种基于岩藻依聚糖的支架,岩藻依聚糖是一种硫酸化多糖,已知在胚胎发育过程中会影响形态发生素梯度,以支持人类胚胎干细胞(hESCs)向心脏谱系分化。选择了一种大孔(孔径200μm)岩藻依聚糖支架来支持hESCs的附着和增殖。使用基于心脏发生形态发生素骨形态发生蛋白2(BMP2)和转化生长因子(TGFβ),随后是肿瘤坏死因子(TNFα)(心脏生成启动的效应器)的方案,我们比较了与培养皿和胚状体(EBs)相比,支架中的心脏分化情况。在第8天,岩藻依聚糖支架支持编码标记胚胎心脏分化早期步骤的转录因子的3个基因NKX2.5(p<0.05)、MEF2C(p<0.01)和GATA4(p<0.01)的表达显著更高,这通过对MEF2C和NKX2.5的流式细胞术分析得到证实。通过Luminex技术证实了岩藻依聚糖支架局部浓缩和缓慢释放TGFβ和TNFα的能力。我们还发现,岩藻依聚糖支架支持以心房钠尿肽(ANF)表达显著更高(p<0.001)为特征的胚胎心脏分化后期,尽管仅观察到罕见的跳动区域。我们推测软水凝胶中缺乏机械应力会损害肌节形成,这通过对心肌肌球蛋白MYH6的分子分析和肌节α - 肌动蛋白的免疫组织化学染色得到证实。尽管如此,岩藻依聚糖支架通过促进平滑肌细胞有助于连接跳动区域的细肌丝的发育,从而使跳动区域能够维持长达6个月。总之,岩藻依聚糖支架似乎是一种非常有前景的生物材料,可用于控制hESCs的心脏分化,并且可以进一步与机械应力相结合,以促进分化末期的肌节形成。