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Promoting effect of small molecules in cardiomyogenic and neurogenic differentiation of rat bone marrow-derived mesenchymal stem cells

机译:小分子对大鼠骨髓间充质干细胞心肌和神经源性分化的促进作用

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Small molecules, growth factors, and cytokines have been used to induce differentiation of stem cells into different lineages. Similarly, demethylating agents can trigger differentiation in adult stem cells. Here, we investigated the in vitro differentiation of rat bone marrow mesenchymal stem cells (MSCs) into cardiomyocytes by a demethylating agent, zebularine, as well as neuronal-like cells by β-mercaptoethanol in a growth factor or cytokines-free media. Isolated bone marrow-derived MSCs cultured in Dulbecco’s Modified Eagle’s Medium exhibited a fibroblast-like morphology. These cells expressed positive markers for CD29, CD44, and CD117 and were negative for CD34 and CD45. After treatment with 1?μM zebularine for 24?hours, the MSCs formed myotube-like structures after 10?days in culture. Expression of cardiac-specific genes showed that treated MSCs expressed significantly higher levels of cardiac troponin-T, Nkx2.5, and GATA-4 compared with untreated cells. Immunocytochemical analysis showed that differentiated cells also expressed cardiac proteins, GATA-4, Nkx 2.5, and cardiac troponin-T. For neuronal differentiation, MSCs were treated with 1 and 10?mM β-mercaptoethanol overnight for 3?hours in complete and serum-free Dulbecco’s Modified Eagle’s Medium, respectively. Following overnight treatment, neuron-like cells with axonal and dendritic-like projections originating from the cell body toward the neighboring cells were observed in the culture. The mRNA expression of neuronal-specific markers, Map2, Nefl, Tau, and Nestin, was significantly higher, indicating that the treated cells differentiated into neuronal-like cells. Immunostaining showed that differentiated cells were positive for the neuronal markers Flk, Nef, Nestin, and β-tubulin.
机译:小分子,生长因子和细胞因子已用于诱导干细胞分化为不同谱系。同样,脱甲基剂可触发成体干细胞分化。在这里,我们研究了在生长因子或无细胞因子培养基中,通过去甲基化剂,zebularine和β-巯基乙醇在体外将大鼠骨髓间充质干细胞(MSCs)分化为心肌细胞,以及神经元样细胞。在Dulbecco的改良Eagle培养基中培养的分离的骨髓间充质干细胞表现出成纤维细胞样的形态。这些细胞表达CD29,CD44和CD117阳性标记,而CD34和CD45阴性。用1?μMzebularine处理24?小时后,MSC在培养10天后便形成了肌管样结构。心脏特异性基因的表达表明,与未处理的细胞相比,处理过的MSC表达的心肌肌钙蛋白T,Nkx2.5和GATA-4的水平明显更高。免疫细胞化学分析显示,分化的细胞还表达心脏蛋白,GATA-4,Nkx 2.5和心脏肌钙蛋白-T。对于神经元分化,分别在完全和无血清的Dulbecco改良Eagle培养基中,分别用1和10?mMβ-巯基乙醇处理MSC 3个小时,过夜。过夜处理后,在培养物中观察到具有轴突和树突状突起的神经元样细胞,其从细胞体向相邻细胞起源。神经元特异性标志物Map2,Nefl,Tau和Nestin的mRNA表达明显更高,表明处理过的细胞分化为神经元样细胞。免疫染色显示,分化的细胞对神经元标记Flk,Nef,Nestin和β-微管蛋白呈阳性。

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