Aspirin promotes osteogenic differentiation of human dental pulp stem cells.
Aspirin promotes osteogenic differentiation of human dental pulp stem cells.
复制标题
阿司匹林促进人牙髓干细胞成骨分化
DOI:
10.3892/ijmm.2018.3801
复制
发表时间:
2018-10
影响因子:
5.4
通讯作者:
Zhang B
中科院分区:
文献类型:
--
作者:
Yuan M;Zhan Y;Hu W;Li Y;Xie X;Miao N;Jin H;Zhang B
Human dental pulp stem cells (hDPSCs) possess self-renewal and osteogenic differentiation properties, and have been used for orofacial bone regeneration and periodontal treatment. Aspirin has been demonstrated to enhance the regeneration of bone marrow mesenchymal stem cells (MSCs); however, the impact of aspirin on the osteogenic differentiation of hDPSCs remains unknown. In the present study, hDPSCs were characterized by flow cytometry, while their clonogenic potential and multipotency were assessed using alizarin red, Oil red O and alcian blue staining. The effect of aspirin on hDPSC viability was assessed using Cell Counting Kit-8 assay. Osteogenic capacity was examined by alkaline phosphatase activity, alizarin red staining, reverse transcription-polymerase chain reaction and western blotting. Furthermore, in vivo cranial defects were established in Sprague-Dawley rats to evaluate the effect of aspirin on hDPSC-based bone regeneration. Anorganic bovine bone was used as a bone replacement material and as the carrier for hDPSCs. New bone formation was observed through radiographic and histological analysis. The study demonstrated that hDPSCs expressed MSC markers and possessed multipotency in vitro. Aspirin was non-toxic to hDPSCs at a concentration of ≤100 μg/ml and enhanced the osteogenesis of hDPSCs in vitro. Aspirin significantly increased hDPSC-based bone formation in the rat cranial defect model at 8 or 12 weeks post-implantation (P<0.05). The data suggested that aspirin promotes the osteogenic potential of hDPSCs in vitro and in vivo. Overall, the present study indicated that aspirin improves the bone regeneration capacity of hDPSCs.
登录
查看更多内容
DOI:
10.1073/pnas.0508480102
发表时间:
2005-11-22
影响因子:
11.1
作者:
Sun, L;Blair, HC;Zaidi, M
通讯作者:
Zaidi, M
影响因子:
7.6
作者:
Liu, Y.;Chen, C.;Shi, S.
通讯作者:
Shi, S.
影响因子:
3.7
作者:
Ferro F;Spelat R;Beltrami AP;Cesselli D;Curcio F
通讯作者:
Curcio F
影响因子:
6.2
作者:
Shi, S;Gronthos, S
通讯作者:
Gronthos, S
DOI:
10.3390/molecules17021219
发表时间:
2012-01-31
期刊:
Molecules (Basel, Switzerland)
影响因子:
--
作者:
Liu M;Sun Y;Liu Y;Yuan M;Zhang Z;Hu W
通讯作者:
Hu W