Taşlı P Neslihan, Doğan Ayşegül, Demirci Selami, Şahin Fikrettin
Department of Genetics and Bioengineering, Faculty of Engineering and Architecture, Yeditepe University, 26 Agustos Campus, Kayisdagi cad., Kayisdagi, 34755, Istanbul, Turkey.
Cytotechnology. 2016 Mar;68(2):319-29. doi: 10.1007/s10616-014-9784-2. Epub 2015 Feb 20.
Stem cells with high proliferation, self-renewal and differentiation capacities are promising for tissue engineering approaches. Among stem cells, human tooth germ stem cells (hTGSCs) having mesenchymal stem cell characteristics are highly proliferative and able to differentiate into several cell lineages. Researchers have recently focused on transplanting stem cells with bioconductive and/or bioinductive materials that can provide cell commitment to the desired cell lineages. In the present study, effects of pluronic block copolymers (F68, F127 and P85) on in vitro myo- and neurogenic differentiation of human tooth germ stem cells (hTGSCs) were investigated. As P85 was found to exert considerable toxicity to hTGSCs even at low concentrations, it was not evaluated for further differentiation experiments. Immunocytochemical analysis, gene and protein expression studies revealed that while F68 treatment increased lineage-specific gene expression in both myo- and neuro-genically differentiated cells, F127 did not result in any remarkable difference compared to cells treated with differentiation medium. Subsequent studies are required to explore the exact mechanisms of how F68 increases the myogenic and neurogenic differentiation of hTGSCs. The present work indicates that pluronic F68 might be used in functional skeletal and neural tissue engineering applications.
具有高增殖、自我更新和分化能力的干细胞在组织工程方法中具有广阔前景。在干细胞中,具有间充质干细胞特征的人牙胚干细胞(hTGSCs)具有高度增殖能力,并能够分化为多种细胞谱系。研究人员最近致力于将干细胞与生物传导性和/或生物诱导性材料一起移植,这些材料能够促使细胞定向分化为所需的细胞谱系。在本研究中,研究了普朗尼克嵌段共聚物(F68、F127和P85)对人牙胚干细胞(hTGSCs)体外肌源性和神经源性分化的影响。由于发现即使在低浓度下P85对hTGSCs也有相当大的毒性,因此未对其进行进一步的分化实验评估。免疫细胞化学分析、基因和蛋白质表达研究表明,虽然F68处理增加了肌源性和神经源性分化细胞中谱系特异性基因的表达,但与用分化培养基处理的细胞相比,F127并未导致任何显著差异。需要进一步的研究来探索F68增加hTGSCs肌源性和神经源性分化的确切机制。目前的研究表明,普朗尼克F68可能用于功能性骨骼和神经组织工程应用。