West China Journal of Stomatology

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Effects of Icariin promotion on proliferation and osteogenic differentiation of human periodontal ligament stem cells

Qin Zishun, Yin Lihua, Wang Kaijuan, Liu Qi, Cheng Wenxiao, Gao Peng, Sun Kemo, Zhong Mei, Yu Zhanhai   

  1. Dept. of Prosthodontics, Medicial College of Stomatology, Lanzhou University, Lanzhou 730000, China
  • Online:2015-08-01 Published:2015-08-01

Abstract:

Objective To evaluate the effects of Icariin (ICA) on the proliferation and osteogenic differentiation of human periodontal ligament stem cells (hPDLSCs) in vitro and in vivo. Methods An enzymatic digestion block was used in vitro to culture hPDLSCs, which were separated and purified by limited dilution cloning. The hPDLSCs were identified using cellsurface markers and cocultured with 1×10−7 mol•L−1 ICA solution. The proliferation ability of these cells was determined by thiazolyl blue tetrazolium bromide (MTT) assay. After staining with alkaline phosphatase (ALP), osteogenesis was detected by enzyme-linked immunosorbent assay. Osteoblast-related genes were analyzed by reverse transcription-polymerase chain reaction. Alizarin red staining was performed to measure the level of calcium deposition. The hPDLSCs were cocultured with 1×10−7 mol•L−1 ICA and nano-hydroxyapatite scaffolds in vivo before transplantation into subcutaneous tissues of nude mice. Osteogenic abilities were histochemically analyzed after 30 days of induction. Results The hPDLSCs were affected by 1×10−7 mol•L−1 ICA, and MTT assay showed that the proliferation of the groups treated with ICA in vitro was better than that of the control groups on the second day. The ALP activity of the treated hPDLSCs was significantly enhanced after cell culture for 3, 5, and 7 days. The gene expression of osteoblastic markers was also significantly enhanced after 7 days. The deposition of mineralization after incubation with 1×10−7 mol•L−1 ICA increased compared with the control after cell culture for 14, 21, and 28 days. Furthermore, the bone expression of the treatment groups in vivo was significantly enhanced compared with that of the control groups. Conclusion Treatment with 1×10−7 mol•L−1 ICA can significantly promote proliferation and differentiation of hPDLSCs in vitro and in vivo. ICA can effectively function as a bioactive growth factor in periodontal tissue engineering to replace traditional growth factors.

Key words: human periodontal ligament stem cells, Icariin, proliferation, differentiation, nano-hydroxyapatite