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首页> 外文期刊>Frontiers in Neuropharmacology >The Synergistic Anti-Apoptosis Effects of Amniotic Epithelial Stem Cell Conditioned Medium and Ponesimod on the Oligodendrocyte Cells
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The Synergistic Anti-Apoptosis Effects of Amniotic Epithelial Stem Cell Conditioned Medium and Ponesimod on the Oligodendrocyte Cells

机译:羊膜上皮干细胞条件培养基和源极型在oligodendrocyte细胞中的协同抗凋亡作用

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摘要

Multiple sclerosis is a chronic inflammatory and neurodegenerative disease of the central nervous system. The current treatment of Multiple sclerosis is based on anti-inflammatory disease-modifying treatments, which can not regenerate myelin and eventually neurons. So, we need new approaches for axonal protection and remyelination. Amniotic epithelial stem cells amniotic epithelial cells, as a neuroprotective and neurogenic agent, are a proper source in tissue engineering and regenerative medicine. Due to differentiation capability and secretion of growth factors, AECs can be a candidate for the treatment of MS. Moreover, sphingosine-1-phosphate (S1P) receptor modulators were recently approved by FDA for MS. Ponesimod is an S1P receptor-1 modulator that acts selectively as an antiinflammatory agent and provides a suitable microenvironment for the function of the other neuroprotective agents. In this study, due to the characteristics of AECs, they are considered a treatment option in MS. The conditioned medium of AECs concurrently with ponesimod was used to evaluate the viability of the oligodendrocyte cell line after induction of cell death by cuprizone. Cell viability after treatment by conditioned medium and ponesimod was increased compared to untreated groups. Also, the results showed that combination therapy with CM and ponesimod had a synergistic anti-apoptotic effect on oligodendrocyte cells. The combination treatment with CM and ponesimod reduced the expression of caspase-3, caspase-8, Bax, and Annexin V proteins and increased the relative BCL-2/Bax ratio, indicating inhibition of apoptosis as a possible mechanism of action. Based on these promising results, combination therapy with amniotic stem cells and ponesimode could be a proper alternative for multiple sclerosis treatment.
机译:多发性硬化是中枢神经系统的慢性炎症和神经变性疾病。目前对多发性硬化的治疗基于抗炎疾病改性治疗,其不能再生髓鞘,最终是神经元。因此,我们需要新的轴突保护和重新选择方法。羊膜上皮干细胞作为神经保护剂和神经发生剂的羊膜上皮细胞是组织工程和再生医学的适当来源。由于差异化能力和生长因子的分泌,AECS可以是治疗MS的候选者。此外,最近通过FDA批准了鞘氨酸-1-磷酸酯(S1P)受体调节剂。 PONESIMOD是一种S1P受体-1调节剂,其选择性地作为抗炎剂作用,并为其他神经保护剂的功能提供合适的微环境。在本研究中,由于AECS的特征,它们被认为是MS中的治疗选择。与源型乳头同时的AEC的调节介质用于评估uigodendrocyte细胞系在诱导铜酮型抑制细胞死亡后的活力。与未处理的基团相比,通过调节培养基和源介质处理后的细胞活力增加。此外,结果表明,用CM和源型的联合治疗对少突细胞细胞具有协同抗凋亡作用。用Cm和源型的组合处理降低了Caspase-3,Caspase-8,Bax和annexin V蛋白的表达,并增加了相对Bcl-2 / Bax比,表明凋亡的抑制作用是可能的作用机制。基于这些有前途的结果,用羊皮细胞和阳极纤维的联合治疗可能是多发性硬化处理的适当替代方案。

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