Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Research Group Neurobiology of Stress Resilience, Max Planck Institute of Psychiatry, Munich, Germany.
Cell Prolif. 2023 Jul;56(7):e13397. doi: 10.1111/cpr.13397. Epub 2023 Jan 11.
The beneficial effects of hair follicle stem cells in different animal models of nervous system conditions have been extensively studied. While chick embryo extract (CEE) has been used as a growth medium supplement for these stem cells, this is the first study to show the effect of CEE on them. The rat hair follicle stem cells were isolated and supplemented with 10% fetal bovine serum plus 10% CEE. The migration rate, proliferative capacity and multipotency were evaluated along with morphometric alteration and differentiation direction. The proteome analysis of CEE content identified effective factors of CEE that probably regulate fate and function of stem cells. The CEE enhances the migration rate of stem cells from explanted bulges as well as their proliferation, likely due to activation of AP-1 and translationally controlled tumour protein (TCTP) by thioredoxin found in CEE. The increased length of outgrowth may be the result of cyclic AMP response element binding protein (CREB) phosphorylation triggered by active CamKII contained in CEE. Further, CEE supplementation upregulates the expression of vascular endothelial growth factor (VEGF), brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor. The elevated expression of target genes and proteins may be due to CREB, AP-1 and c-Myc activation in these stem cells. Given the increased transcript levels of neurotrophins, VEGF, and the expression of PDGFR-α, S100B, MBP and SOX-10 protein, it is possible that CEE promotes the fate of these stem cells towards Schwann cells.
毛囊干细胞在不同的神经系统疾病动物模型中的有益作用已被广泛研究。虽然鸡胚提取物 (CEE) 已被用作这些干细胞的生长培养基补充物,但这是第一项研究表明 CEE 对它们的影响。分离大鼠毛囊干细胞,并添加 10%胎牛血清加 10% CEE。评估迁移率、增殖能力和多能性以及形态改变和分化方向。CEE 内容物的蛋白质组分析确定了 CEE 的有效因素,这些因素可能调节干细胞的命运和功能。CEE 增强了从外植体隆起中分离出来的干细胞的迁移率及其增殖能力,这可能是由于 CEE 中存在的硫氧还蛋白激活了 AP-1 和翻译控制肿瘤蛋白 (TCTP)。突起的长度增加可能是由于 CEE 中存在的活性 CamKII 触发环腺苷酸反应元件结合蛋白 (CREB) 磷酸化所致。此外,CEE 补充上调血管内皮生长因子 (VEGF)、脑源性神经营养因子和神经胶质细胞源性神经营养因子的表达。这些干细胞中 CREB、AP-1 和 c-Myc 的激活可能导致靶基因和蛋白的表达上调。鉴于神经营养因子、VEGF 的转录水平增加,以及 PDGFR-α、S100B、MBP 和 SOX-10 蛋白的表达,CEE 可能促进这些干细胞向施万细胞的命运。