血管内皮生长因子(VEGF)对牙髓干细胞(DPSC)的影响

E. Mullins, Cale Forgues, K. Kingsley
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引用次数: 8

摘要

牙髓干细胞(DPSCs)是一种非胚胎间充质干细胞,在治疗和再生生物医学应用方面具有重要的潜力。对DPSC分化的研究表明,利用细胞因子和生长因子(如血管内皮生长因子(VEGF)), DPSC有可能形成多种组织类型,包括神经、成骨和血管前体。8个先前分离的牙髓干细胞(DPSC)分离物在培养物中生长并用VEGF处理以评估其对生长,活力或生物标志物表达的影响。10 ng/mL的VEGF可显著抑制两种快速分裂或rDT DPSC分离株的生长,而在中间(iDT)或缓慢(sDT)生长的DPSC分离株中没有其他可测量的影响。此外,VEGF对sDT或iDT DPSC分离株的生存能力没有显著影响,然而,所有三种快速分裂或rDT DPSC分离株的生存能力均显着提高。最后,观察成骨生物标志物碱性磷酸酶(ALP)和牙本质唾液蛋白(DSPP)的mRNA表达,并观察DPSC生物标志物的特定组合表达(NANOG与Sox-2或Oct-4联合表达,但不同时表达)。这些数据的结果表明,VEGF可能足以诱导DPSC分离物的部分分化,尽管这可能取决于DPSCs的MSC生物标志物表达。这些初步数据可以进一步研究组织再生和生物工程的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Vascular Endothelial Growth Factor (VEGF) on Dental Pulp Stem Cells (DPSC)
Dental Pulp Stem Cells (DPSCs) are non-embryonic, mesenchymal stem cells that may have significant potential for therapeutic and regenerative biomedical applications. Studies of DPSC differentiation have demonstrated the potential to form many tissue types, including neural, osteogenic and vascular precursors using cytokines and growth factors, such as Vascular Endothelial Growth Factor (VEGF). Eight previously isolated Dental Pulp Stem Cell (DPSC) isolates were grown in culture and treated with VEGF to evaluate any effects on growth, viability or biomarker expression. Administration of VEGF at 10 ng/mL significantly inhibited growth in two rapidly dividing or rDT DPSC isolates, with no other measurable effects noted among the intermediate (iDT) or slow (sDT) growing DPSC isolates. In addition, administration of VEGF had no significant effects on viability of the sDT or iDT DPSC isolates, however, all three of the rapidly dividing or rDT DPSC isolates exhibited significantly increased viability. Finally, mRNA expression of osteogenic biomarkers Alkaline Phosphatase (ALP) and Dentin Sialophosphoprotein (DSPP) was observed among the rDT isolates with specific combinations of DPSC biomarkers expressed (NANOG in combination with Sox-2 or Oct-4 but not both). The results of these data suggest that VEGF administration may be sufficient to induce partial differentiation of DPSC isolates, although this may be dependent upon the MSC biomarker expression of the DPSCs. These preliminary data may further research into the potential for tissue regeneration and bioengineering.
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