神经分化的创新途径:硫酸软骨素和软骨素酶诱导人诱导多能干细胞的分化。

IF 2.2
Mohsen Ghiasi, Mohammad-Taher Moradi, Raheleh Halabian, Marzieh Ghollasi, Abdolreza Dayani
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引用次数: 0

摘要

背景:干细胞最近在再生医学,特别是在神经系统疾病的治疗中获得了突出的地位。因此,人诱导多能干细胞(human induced Pluripotent Stem Cells, hiPSCs)已成为一个重要的研究热点。目的:利用福斯可林和视黄酸在硫酸软骨素4和软骨素酶联合诱导培养基中诱导hipsc向体外神经谱系分化。方法:采用MTT法和吖啶橙/溴化乙啶(AO/EB)染色法确定最佳成分浓度。随后,采用Real-time PCR分析和免疫荧光染色评估神经特异性基因(NSE、MAP-2、β-微管蛋白III、Oligo-2和GFAP)和蛋白(γ烯醇化酶、MAP-2和β-微管蛋白III),对分化细胞进行全面评估。结果:我们的研究表明,在分化的第7天和第14天,联合使用硫酸软骨素4和软骨素酶可以显著增强神经特异性基因和蛋白质标记,与使用分离酶或底物相比,显示出更高的功效。结论:这些发现强调了硫酸软骨素4和软骨素酶作为促进hipsc神经分化的重要因素的潜在重要性。硫酸软骨素可能激活细胞信号通路,有效诱导神经分化。我们在这项研究中的发现为推进神经系统疾病的再生治疗提供了新的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Innovative Approaches to Neural Differentiation: Chondroitin 4-Sulfate and Chondroitinase Induce Differentiation in Human-induced Pluripotent Stem Cells.

Background: Stem cells have recently gained prominence in regenerative medicine, particularly in the treatment of neurological disorders. As a result, Human-induced Pluripotent Stem Cells (hiPSCs) have become a significant focus.

Objective: This study aimed to differentiate hiPSCs into neural lineages under in vitro conditions using forskolin and retinoic acid in an induction medium combined with chondroitin 4-sulfate and chondroitinase.

Methods: Optimal component concentrations were determined using the MTT assay and acridine orange/ethidium bromide (AO/EB) staining. Subsequently, neural-specific genes (NSE, MAP-2, β-tubulin III, Oligo-2, and GFAP) and proteins (gamma enolase, MAP-2, and β-tubulin III) were assessed using Real-time PCR analysis and immunofluorescence staining to provide a comprehensive evaluation of differentiated cells.

Results: Our study demonstrated a significant enhancement in neural-specific gene and protein markers during the 7th and 14th days of differentiation in the presence of combined chondroitin 4-sulfate and chondroitinase, demonstrating a higher efficacy compared with the application of isolated enzymes or substrates.

Conclusion: These findings emphasize the potential importance of chondroitin 4-sulfate and chondroitinase as important factors in promoting the neural differentiation of hiPSCs. It seems that chondroitin 4-sulfate may activate cellular signaling pathways that are effective in inducing neural differentiation. Our findings in this research provide new opportunities to advance regenerative therapies for neurological disorders.

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