Zhao Sheng-nan, Liu Wen-fei, Zhang Zhen-ting
Department of Prosthodontics, Capital Medical University School of Stomatology, Beijing, China.
Zhonghua Kou Qiang Yi Xue Za Zhi. 2013 Mar;48(3):177-82.
To evaluate the effects of different concentrations of platelet-rich plasma (PRP) on human dental pulp stem cells (hDPSC) proliferation and osteogenic differentiation activity so as to provide basis for future application of dental pulp stem cells and PRP in tissue engineering and bone repair therapy.
hDPSC were isolated and cultivated in vitro. Flow cytometric analysis was carried out to test the expression of STRO-1.hDPSC were cultured in various concentrations of PRP (1%, 5%, 10%, 20%). At the 2nd and 6th day 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) was tested. Osteogenic differentiation of hDPSC was assessed using alkaline phosphatase (ALP) staining and Alizarin Red staining at the 7th and 14th day.
Flow cytometric analysis demonstrated that 14.82% of hDPSC were STRO-1 positive. One percent to 20% PRP showed significant effect of promoting hDPSC proliferation. One percent to 10% PRP showed significant effect of promoting hDPSC osteogenic differentiation.
Certain concentrations of PRP can promote hDPSC proliferate and osteogenic differentiate, and this finding suggests future application of dental pulp stem cells and PRP in bone tissue engineering.
评估不同浓度富血小板血浆(PRP)对人牙髓干细胞(hDPSC)增殖及成骨分化活性的影响,为牙髓干细胞和PRP在组织工程及骨修复治疗中的未来应用提供依据。
体外分离培养hDPSC。进行流式细胞术分析以检测STRO-1的表达。将hDPSC培养于不同浓度(1%、5%、10%、20%)的PRP中。在第2天和第6天进行3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)检测。在第7天和第14天使用碱性磷酸酶(ALP)染色和茜素红染色评估hDPSC的成骨分化情况。
流式细胞术分析表明14.82%的hDPSC为STRO-1阳性。1%至20%的PRP显示出促进hDPSC增殖的显著作用。1%至10%的PRP显示出促进hDPSC成骨分化的显著作用。
一定浓度的PRP可促进hDPSC增殖和成骨分化,这一发现提示牙髓干细胞和PRP在骨组织工程中的未来应用前景。