Journal of Tissue Engineering and Reconstructive Surgery ›› 2019, Vol. 15 ›› Issue (6): 389-392.doi: 10.3969/j.issn.1673-0364.2019.06.004

• Original article • Previous Articles     Next Articles

Effect and Mechanism of Adenosine Triphosphate on Differentiation of Bone Marrow Mesenchymal Stem Cells into Chondrocytes

LEI Jie,HE Chengjian,HE Mengyin   

  1. Department of Joint and Sports Medicine,Bone Trauma Diagnosis and Treatment Center, Hubei Traditional Chinese Medicine Hospital;Treatment of Bone and Joint Diseases by Integrated Traditional Chinese and Western Medicine, Hubei Traditional Chinese Medicine Hospital;Radiology Department, Hubei Traditional Chinese Medicine Hospital
  • Received:2019-09-07 Revised:2019-10-20 Online:2019-12-20 Published:2019-12-20

Abstract: Objective To investigate the effect of adenosine triphosphate on the differentiation of BMSCs into chondrocytes and its mechanism. Methods The primary cells of BMSCs from 4-5 weeks old SD rats were cultured to the third generation in vitro. PNPP method was used to detect the effects of ATP with different concentrations(150, 300 and 600μmol/L) and BBG(receptor inhibitor of P2X7) of on alkaline phosphatase expression in BMSCs. The mRNA expression of multiple cartilage markers was detected by semi-quantitative reverse transcription polymerase chain reaction and real time PCR. Results After ATP was added, the expression of alkaline phosphatase in BMSCs was significantly increased(P<0.05).The highest expression of alkaline phosphatase was observed when ATP concentration was 150 and 300 μmol/L(P<0.05).The expression levels of indicators such as SOX6, SOX9 and COL2A1 were increased(P<0.05). After the addition of P2X7 receptor inhibitor, the promotion effect of ATP on alkaline phosphatase decreased(P <0.05), and the expressions of chondrogenic indicators such as SOX6, SOX9 and COL2A1 were also significantly decreased(P <0.05). Conclusion A certain concentration of ATP can promote the differentiation of bone marrow mesenchymal cells into chondrocytes, which may play a role through the mediation of P2X7 receptor.

Key words: Adenosine triphosphate, Bone marrow derived mesenchymal stem cells, Chondrogenic differentiation

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