Chinese Journal of Tissue Engineering Research ›› 2022, Vol. 26 ›› Issue (30): 4862-4866.doi: 10.12307/2022.767

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Effect of transforming growth factor-beta 3 and bone morphogenetic protein-2 on proliferation and osteogenic differentiation of dental pulp stem cells

Ailimaierdan·Ainiwaer1, Muhetaer·Huojia2, Wang Ling1    

  1. 1Department of Oral Surgery, First Affiliated Hospital (Affiliated Stomatological Hospital) of Xinjiang Medical University, Urumqi 830011, Xinjiang Uygur Autonomous Region, China; 2Oral Center, Shenzhen Luohu People’s Hospital, The Third Affiliated Hospital of Shenzhen University, Shenzhen 518001, Guangdong Province, China
  • Received:2021-09-09 Accepted:2021-11-04 Online:2022-10-28 Published:2022-03-29
  • Contact: Wang Ling, Chief physician, Associate professor, Master’s supervisor, Department of Oral Surgery, First Affiliated Hospital (Affiliated Stomatological Hospital) of Xinjiang Medical University, Urumqi 830011, Xinjiang Uygur Autonomous Region, China
  • About author:Ailimaierdan·Ainiwaer, Master, Physician, Department of Oral Surgery, First Affiliated Hospital (Affiliated Stomatological Hospital) of Xinjiang Medical University, Urumqi 830011, Xinjiang Uygur Autonomous Region, China
  • Supported by:
    the National Natural Science Foundation of China, No. 81560180 (to MH)

Abstract: BACKGROUND: Less is reported about the effect of transforming growth factor-beta 3 and bone morphogenetic protein-2 on the proliferation and osteogenic differentiation of dental pulp stem cells.  
OBJECTIVE: To explore the effect of transforming growth factor-beta 3 and bone morphogenetic protein-2 on the osteogenic differentiation of dental pulp stem cells and its preliminary mechanism.
METHODS:  Dental pulp stem cells were isolated from the pulp tissue of New Zealand rabbit by the enzymatic digestion method. Dental pulp stem cells at passage 3 were divided into the blank group, bone morphogenetic protein-2 group (80 μg/L) and transforming growth factor-beta 3 group (80 μg/L). The cell proliferation activity in each group was tested by MTT assay. After 7 and 14 days of culture, alkaline phosphatase activities were measured. Runt-related transcription factor 2 and bone sialoprotein protein expression levels were conducted by immunocytochemical staining. Osteogenesis-related gene expression was tested through RT-qPCR method. Alizarin red S staining was conducted after 14 and 21 days of culture to observe mineralized nodules.  
RESULTS AND CONCLUSION: (1) Dental pulp stem cell proliferation activity and alkaline phosphatase activity were higher in the bone morphogenetic protein-2 and transforming growth factor-beta 3 groups than those in the blank group (P < 0.05). The alkaline phosphatase activity of the transforming growth factor-beta 3 group on day 7 was higher than that of the bone morphogenetic protein-2 group (P < 0.05). (2) The expression levels of Runt-related transcription factor 2 and bone sialoprotein in the transforming growth factor-beta 3 group and the bone morphogenetic protein-2 group were higher than those in the blank group (P < 0.05). The protein expression of Runt-related transcription factor 2 in the transforming growth factor-beta 3 group on day 7 was higher than that in the bone morphogenetic protein-2 group (P < 0.05). (3) The expression levels of alkaline phosphatase, type I collagen A1, Runt-related transcription factor 2, osteocalcin, osteopontin and Osx genes in the transforming growth factor-beta 3 group and bone morphogenetic protein-2 group were higher than those in the blank group (P < 0.05). On day 7, the expression levels of alkaline phosphatase, type I collagen A1, and Runt-related transcription factor 2 genes of transforming growth factor-beta 3 group were higher than those of bone morphogenetic protein-2 group (P < 0.05). (4) The mineralized nodules in the transforming growth factor-beta 3 group and bone morphogenetic protein-2 group were more obvious than those in the blank group. (5) The results show that transforming growth factor-beta 3 and bone morphogenetic protein-2 can improve the proliferation and osteogenic differentiation of dental pulp stem cells. The osteogenic induction ability of transforming growth factor-beta 3 on dental pulp stem cells was better than that of bone morphogenetic protein-2 at the early stage of osteogenesis.

Key words: transforming growth factor-beta 3, bone morphogenetic protein-2, dental pulp stem cells, proliferation, osteogenic differentiation

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