Harbin Medical University, The First Affiliated Hospital, Department of Endodontics, Harbin, China.
Harbin Medical University, The First Affiliated Hospital, Department of Oral and Maxillofacial Surgery, Harbin, China.
Braz Oral Res. 2019 Oct 28;33:e059. doi: 10.1590/1807-3107bor-2019.vol33.0059. eCollection 2019.
We recently demonstrated that a co-culture system of human umbilical vein endothelial cells (HUVECs) and human dental pulp stem cells (hDPSCs) could enhance angiogenesis ability in vitro. However, whether tumor necrosis factor α (TNF-α) could promote blood vessel formation during pulp regeneration remained unknown. The aim of this study was to investigate the effects of TNF-α on the formation of endothelial tubules and vascular networks in a co-culture system of hDPSCs and HUVECs. hDPSCs were co-cultured with HUVECs at a ratio of 1:5. The Matrigel assay was performed to detect the total tubule branching lengths and numbers of branches, and the Cell-Counting Kit 8 assay was performed to examine the effect of TNF-α on cell proliferation. Real-time polymerase chain reactions and western blot were used to detect vascular endothelial growth factor (VEGF) mRNA and protein expression. The Matrigel assay showed significantly greater total branching lengths and numbers of branches formed in the experimental groups treated with different concentrations of TNF-α compared with the control group. The decomposition times of the tubule structures were also significantly prolonged (P < 0.05). Treatment with 50 ng/ml TNF-α did not significantly change the proliferation of co-cultured cells, but it significantly increased the VEGF mRNA and protein expression levels (p < 0.05). In addition, the migration abilities of HUVECs and hDPSCs increased after co-culture with TNF-α (p < 0.05). TNF-α enhanced angiogenic ability in vitro in the co-culture system of hDPSCs and HUVECs.
我们最近证明,人脐静脉内皮细胞(HUVEC)和人牙髓干细胞(hDPSC)的共培养系统可以增强体外的血管生成能力。然而,肿瘤坏死因子α(TNF-α)是否能在牙髓再生过程中促进血管形成尚不清楚。本研究旨在探讨 TNF-α对 hDPSC 和 HUVEC 共培养系统中内皮小管和血管网络形成的影响。hDPSC 与 HUVEC 以 1:5 的比例共培养。采用 Matrigel 实验检测总小管分支长度和分支数,采用细胞计数试剂盒 8 检测 TNF-α对细胞增殖的影响。实时聚合酶链反应和 Western blot 检测血管内皮生长因子(VEGF)mRNA 和蛋白表达。Matrigel 实验结果显示,与对照组相比,不同浓度 TNF-α处理的实验组形成的总分支长度和分支数明显增加。小管结构的分解时间也明显延长(P < 0.05)。50ng/ml TNF-α处理对共培养细胞的增殖没有显著影响,但显著增加了 VEGF mRNA 和蛋白的表达水平(p < 0.05)。此外,与 TNF-α共培养后 HUVEC 和 hDPSC 的迁移能力也增加(p < 0.05)。TNF-α增强了 hDPSC 和 HUVEC 共培养系统的体外血管生成能力。