Muoio Francesco, Panella Stefano, Jossen Valentin, Lindner Matias, Harder Yves, Müller Michele, Eibl Regine, Tallone Tiziano
Foundation for Cardiological Research and Education (FCRE), Cardiocentro Ticino Foundation, 6807 Taverne, Switzerland.
Institute of Chemistry & Biotechnology, Competence Center of Biochemical Engineering & Cell Cultivation Technique Zurich University of Applied Sciences, 8820 Wädenswil, Switzerland.
J Funct Biomater. 2021 Apr 16;12(2):25. doi: 10.3390/jfb12020025.
Human adipose stem cells (hASCs) are promising candidates for cell-based therapies, but they need to be efficiently expanded in vitro as they cannot be harvested in sufficient quantities. Recently, dynamic bioreactor systems operated with microcarriers achieved considerable high cell densities. Thus, they are a viable alternative to static planar cultivation systems to obtain high numbers of clinical-grade hASCs. Nevertheless, the production of considerable biomass in a short time must not be achieved to the detriment of the cells' quality. To facilitate the scalable expansion of hASC, we have developed a new serum- and xeno-free medium () and a biodegradable microcarrier (). In this study, we investigated whether the culture of hASCs in defined serum-free conditions on microcarriers (3D) or on planar (2D) cell culture vessels may influence the expression of some marker genes linked with the immature degree or the differentiated status of the cells. Furthermore, we investigated whether the biomaterials, which form our biodegradable MCs, may affect cell behavior and differentiation. The results confirmed that the quality and the undifferentiated status of the hASCs are very well preserved when they grow on MCs in defined serum-free conditions. Indeed, the ASCs showed a gene expression profile more compatible with an undifferentiated status than the same cells grown under standard planar conditions.
人脂肪干细胞(hASCs)是基于细胞的治疗方法中很有前景的候选细胞,但由于无法收获足够数量的细胞,它们需要在体外高效扩增。最近,使用微载体操作的动态生物反应器系统实现了相当高的细胞密度。因此,它们是获得大量临床级hASCs的静态平面培养系统的可行替代方案。然而,在短时间内大量生产生物量绝不能以损害细胞质量为代价。为了促进hASC的可扩展扩增,我们开发了一种新的无血清和无异种成分培养基()和一种可生物降解的微载体()。在本研究中,我们调查了在微载体(3D)上或平面(2D)细胞培养容器中在限定的无血清条件下培养hASCs是否会影响与细胞未成熟程度或分化状态相关的一些标记基因的表达。此外,我们研究了构成我们可生物降解微载体的生物材料是否会影响细胞行为和分化。结果证实,当hASCs在限定的无血清条件下在微载体上生长时,其质量和未分化状态得到了很好的保留。事实上,与在标准平面条件下生长的相同细胞相比,脂肪干细胞显示出与未分化状态更相符的基因表达谱。