Advanced Tissue Engineering and Stem Cell Biology Group, School of Life Sciences, University of Technology Sydney, Ultimo, NSW 2007, Australia.
Neural Injury Research Unit, School of Life Sciences, University of Technology Sydney, Ultimo, NSW 2007, Australia.
Int J Mol Sci. 2023 Nov 13;24(22):16269. doi: 10.3390/ijms242216269.
Adipose-derived stem cells (ADSCs) have incredible potential as an avenue to better understand and treat neurological disorders. While they have been successfully differentiated into neural stem cells and neurons, most such protocols involve 2D environments, which are not representative of in vivo physiology. In this study, human ADSCs were cultured in 1.1 kPa polyethylene-glycol 3D hydrogels for 10 days with B27, CultureOne (C1), and N2 neural supplements to examine the neural differentiation potential of ADSCs using both chemical and mechanical cues. Following treatment, cell viability, proliferation, morphology, and proteome changes were assessed. Results showed that cell viability was maintained during treatments, and while cells continued to proliferate over time, proliferation slowed down. Morphological changes between 3D untreated cells and treated cells were not observed. However, they were observed among 2D treatments, which exhibited cellular elongation and co-alignment. Proteome analysis showed changes consistent with early neural differentiation for B27 and C1 but not N2. No significant changes were detected using immunocytochemistry, potentially indicating a greater differentiation period was required. In conclusion, treatment of 3D-cultured ADSCs in PEG-based hydrogels with B27 and C1 further enhances neural marker expression, however, this was not observed using supplementation with N2.
脂肪来源干细胞 (ADSCs) 在更好地理解和治疗神经紊乱方面具有令人难以置信的潜力。虽然它们已经成功地分化为神经干细胞和神经元,但大多数此类方案都涉及二维环境,这与体内生理学并不相符。在这项研究中,使用 B27、CultureOne(C1)和 N2 神经补充剂将人 ADSC 培养在 1.1 kPa 的聚乙二醇 3D 水凝胶中 10 天,以利用化学和机械线索来研究 ADSC 的神经分化潜力。处理后,评估细胞活力、增殖、形态和蛋白质组变化。结果表明,处理过程中保持了细胞活力,虽然细胞随时间继续增殖,但增殖速度减慢。未观察到 3D 未处理细胞和处理细胞之间的形态变化。然而,在 2D 处理中观察到了这种变化,其表现为细胞伸长和共对准。蛋白质组分析表明,B27 和 C1 处理与早期神经分化一致,但 N2 处理则不一致。免疫细胞化学检测未检测到明显变化,可能表明需要更长的分化时间。总之,用 B27 和 C1 对 3D 培养的 ADSC 进行 PEG 基水凝胶处理进一步增强了神经标志物的表达,但用 N2 补充则没有观察到这种情况。