Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Clinical Neurology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Neurosci Lett. 2019 Jun 21;704:8-14. doi: 10.1016/j.neulet.2019.03.033. Epub 2019 Mar 20.
Effective delivery of trophic factors to cure neurological disorders and traumatic injuries is a major challenge. With promising therapeutic effects of epidermal neural crest stem cells (EPI-NCSCs) in preclinical spinal cord injury, there is an implication that these stem cells might provide supportive role through releasing various trophic agents. Hence, the present study was designed to assess the influence of valproic acid (VPA), a well-known histone deacetylases inhibitor, on mRNA expression of selected trophic factors. In this study, following stem cell migration from explanted hair bulges, immunostaining against Nestin, SOX-10, DCX, β-III tubulin and GFAP was carried out. Then, cells were treated with various clinically relevant concentrations of VPA and the survival rate was defined by MTT assay. Finally, stem cells were treated with 0.1 and 1 mM VPA and the drug impact on the transcription level of BDNF, GDNF, VEGF, NGF and NT3 at 6, 24, 72, 168 h was assessed by quantitative real-time PCR. The examined proteins expressions in the population of migrated cells confirmed the identity of stem cells as EPI-NCSCs. In addition, MTT assay showed that all three tested concentrations of VPA were suitable to treat these cells. Trophic factors assessment, following treatment revealed the mRNA expression level of BDNF, GDNF and VEGF could be significantly up- regulated at various time points, mainly by 1 mM VPA. However, NGF and NT3 transcripts were enhanced at few limited time points. Our findings showed that EPI-NCSCs due to secretion of various trophic factors are potential candidate to deliver the required trophic agents and their potential can be enhanced by 1 mM VPA, predominantly following 168 h treatment. Hence, these cells can be utilized to modulate destructive context of neurological disorders and injuries.
有效递送达营养因子以治疗神经紊乱和创伤性损伤是一个主要的挑战。表皮神经嵴干细胞(EPI-NCSCs)在临床前脊髓损伤中具有有前景的治疗效果,这暗示这些干细胞可能通过释放各种营养因子来提供支持作用。因此,本研究旨在评估众所周知的组蛋白去乙酰化酶抑制剂丙戊酸(VPA)对选定营养因子的 mRNA 表达的影响。在这项研究中,在干细胞从毛囊隆起中迁移出来后,进行针对巢蛋白、SOX-10、DCX、β-III 微管蛋白和 GFAP 的免疫染色。然后,用各种临床相关浓度的 VPA 处理细胞,并通过 MTT 测定法定义存活率。最后,用 0.1 和 1mM VPA 处理干细胞,并通过定量实时 PCR 评估药物对 BDNF、GDNF、VEGF、NGF 和 NT3 的转录水平的影响。在迁移细胞群体中检测到的蛋白质表达证实了这些细胞为 EPI-NCSCs 的身份。此外,MTT 测定法表明,VPA 的三种测试浓度均适合治疗这些细胞。治疗后对营养因子的评估表明,BDNF、GDNF 和 VEGF 的 mRNA 表达水平可以在各个时间点显著上调,主要是通过 1mM VPA。然而,NGF 和 NT3 转录本仅在少数有限的时间点增强。我们的研究结果表明,EPI-NCSCs 由于分泌各种营养因子,是递送达所需营养因子的潜在候选物,并且它们的潜力可以通过 1mM VPA 增强,主要是在 168 小时治疗后。因此,这些细胞可用于调节神经紊乱和损伤的破坏性环境。