缺氧条件下牙源性干细胞分泌VEGF、TGF-B1和IGF-1的研究

P. Cooper, B. Scheven
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引用次数: 0

摘要

牙源性干细胞(DSC)是组织破坏后组织再生的重要细胞。缺氧是损伤组织的环境条件之一,但缺氧对DSC的影响尚不完全清楚。目的:探讨缺氧对牙源性干细胞生长因子生成及表达的影响。方法:将大鼠牙周韧带干细胞(PDLSCs)和牙髓干细胞(DPSCs)在无血清培养基中培养2、3 d。当细胞达到70%融合时,在常氧(21%)或缺氧(2%)条件下孵育,然后收集含有细胞分泌组的条件培养基(CM)并与骨髓干细胞(BMSCs)进行比较。采用ELISA试剂盒检测收集的CM中VEGF、TGF-β 1和IGF-1水平。然后用逆转录聚合酶链反应(RT-PCR)测定生长因子的基因表达。结果:缺氧培养使牙源性干细胞分泌生长因子增加,VEGF和TGF-β1基因表达分析也支持上述发现。有趣的是,IGF-1仅在PDLSC CM中检测到,与DPSCs和BMSCs相比,PDLSC中IGF-1基因表达显著,且与IGF-BP1表达呈反比关系,这也支持了这些数据。低氧培养不影响骨髓间充质干细胞分泌TGF-β 1。结论:牙源性干细胞缺氧培养可改变分泌组中生长因子的含量,且IGF-1仅在PDLSC分泌组中检测到
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Secretion of VEGF, TGF-B1 and IGF-1 by Dental- Derived Stem Cells under Hypoxic Conditions
Dental-derived stem cells (DSC) are important cells in tissue regeneration following tissue destruction. One of the environmental conditions in the injured tissue is reduce in oxygen level (hypoxia) but the effect of hypoxia on the DSC is not fully elucidated. Objectives: This study aims to evaluate the effect of hypoxia on growth factor production and expression of dental-derived stem cells. Methods : Rat periodontal ligament stem cells (PDLSCs) and dental pulp stem cells (DPSCs) were cultured in serum-free media for two or three days. When the cells achieved 70% confluence, they were incubated under normoxia (21%) or hypoxia (2%) conditions, before the conditioned media (CM) that contained the cells’ secretomes were collected and compared with bone marrow stem cells (BMSCs).ELISA kits were used to analyze VEGF, TGF-β 1 and IGF-1 levels in the collected CM. The reverse transcriptase-polymerase chain reaction (RT-PCR) was then used to determine the gene expression of the growth factors. Results : Hypoxia incubation increased growth factor secretion by the dental-derived stem cells, and these findings were also supported by the gene expression analysis of VEGF and TGF-β1 . Interestingly, IGF-1 was only detected in PDLSC CM, and these data were supported by prominent IGF-I gene expression and an inverse relationship with IGF-BP1 expression by PDLSC, compared with DPSCs and BMSCs. TGF-β 1 secretion by BMSCs was not influenced by hypoxic incubation. Conclusion : Hypoxic incubation of the dental-derived stem cells alters growth factor content in the secretomes, and IGF-1 was only detected in the PDLSC secretome
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