Department of Pharmacology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mol Neurobiol. 2021 Oct;58(10):5327-5337. doi: 10.1007/s12035-021-02423-9. Epub 2021 Jul 23.
Schwann cells (SCs) are considered potentially attractive candidates for transplantation therapies in neurodegenerative diseases. However, problems arising from the isolation and expansion of the SCs restrict their clinical applications. Establishing an alternative Schwann-like cell type is a prerequisite. Epidermal neural crest stem cells (EPI-NCSCs) are well studied for their autologous accessibility, along with the ability to produce major neural crest derivatives and neurotrophic factors. In the current study, we explored insulin influence, a well-known growth factor, on directing EPI-NCSCs into the Schwann cell (SC) lineage. EPI-NCSCs were isolated from rat hair bulge explants. The viability of cells treated with a range of insulin concentrations (0.05-100 μg/ml) was defined by MTT assay at 24, 48, and 72 h. The gene expression profiles of neurotrophic factors (BDNF, FGF-2, and IL-6), key regulators involved in the development of SC (EGR-1, SOX-10, c-JUN, GFAP, OCT-6, EGR-2, and MBP), and oligodendrocyte (PDGFR-α and NG-2) were quantified 1 and 9 days post-treatment with 0.05 and 5 μg/ml insulin. Furthermore, the protein expression of nestin (stemness marker), SOX-10, PDGFR-α, and MBP was analyzed following the long-term insulin treatment. Insulin downregulated the early-stage SC differentiation marker (EGR-1) and increased neurotrophins (BDNF and IL-6) and pro-myelinating genes, including OCT-6, SOX-10, EGR-2, and MBP, as well as oligodendrocyte differentiation markers, upon exposure for 9 days. Insulin can promote EPI-NCSC differentiation toward SC lineage and possibly oligodendrocytes. Thus, employing insulin might enhance the EPI-NCSCs efficiency in cell transplantation strategies.
许旺细胞 (SCs) 被认为是神经退行性疾病移植治疗中具有潜在吸引力的候选细胞。然而,SCs 的分离和扩增所带来的问题限制了它们的临床应用。建立替代许旺样细胞类型是前提。表皮神经嵴干细胞 (EPI-NCSCs) 因其自体可用性以及产生主要神经嵴衍生物和神经营养因子的能力而得到广泛研究。在本研究中,我们探讨了胰岛素对 EPI-NCSCs 向许旺细胞 (SC) 谱系分化的影响。EPI-NCSCs 从大鼠毛囊隆起外植体中分离得到。通过 MTT 测定法在 24、48 和 72 h 时测定细胞处理不同浓度胰岛素(0.05-100μg/ml)后的细胞活力。通过 qPCR 检测神经营养因子(BDNF、FGF-2 和 IL-6)、SC 发育关键调控因子(EGR-1、SOX-10、c-JUN、GFAP、OCT-6、EGR-2 和 MBP)和少突胶质细胞(PDGFR-α和 NG-2)的基因表达谱在 0.05 和 5μg/ml 胰岛素处理后 1 天和 9 天。此外,在长期胰岛素处理后分析巢蛋白(干性标志物)、SOX-10、PDGFR-α和 MBP 的蛋白表达。胰岛素下调早期 SC 分化标志物(EGR-1),并增加神经营养因子(BDNF 和 IL-6)和促髓鞘形成基因,包括 OCT-6、SOX-10、EGR-2 和 MBP,以及少突胶质细胞分化标志物,在暴露 9 天后。胰岛素可以促进 EPI-NCSC 向 SC 谱系和可能的少突胶质细胞分化。因此,在细胞移植策略中使用胰岛素可能会提高 EPI-NCSCs 的效率。