The effects and mechanism of paeoniflorin in promoting osteogenic differentiation of MC3T3-E1.

J Orthop Surg Res

Department of Rehabilitation Medicine, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, No. 136, Jingzhou Road, Xiangyang, 441021, Hubei, China.

Published: February 2022

AI Article Synopsis

  • The study explores how paeoniflorin, from Traditional Chinese Medicine, can enhance the osteogenic differentiation of MC3T3-E1 cells, which are precursor cells for bone formation, to address increasing osteoporosis rates.
  • Researchers assessed paeoniflorin’s effects by testing different concentrations and using various staining and analysis methods to measure its impact on gene and protein expression related to bone formation, particularly focusing on the Wnt/β-catenin signaling pathway.
  • The results indicated that paeoniflorin is non-toxic up to 100 μM, significantly boosts osteogenic differentiation in a dose-dependent manner, and affects key signaling pathways, with DKK-1 showing that Wnt/β-catenin is involved

Article Abstract

Background: The incidence of osteoporosis and osteoporotic fractures is increasing every year. Traditional Chinese Medicine (TCM) can shed new light on the treatment of osteoporosis. This study aimed to explore the role and mechanism of paeoniflorin in promoting osteogenic differentiation of an osteoblast precursor cell line (MC3T3-E1).

Methods: MC3T3-E1 cells were cultured in osteogenic induction medium (OIM) and OIM combined with different concentrations of paeoniflorin. The optimal dose of paeoniflorin was assessed by a cell counting kit-8 (CCK-8) assay. Then, alkaline phosphatase (ALP) and Alizarin Red S (ARS) staining were performed to assess the osteogenic capacity of paeoniflorin. The transcription of osteogenic genes and the expression of osteogenic proteins were assessed by RT-PCR and Western blotting, respectively. The transcription of Wnt/β-catenin signaling pathway genes and proteins was assessed by RT-PCR and Western blotting, respectively. Finally, Dickkopf-1 (DKK-1), a Wnt/β-catenin signaling pathway inhibitor, was used to identify whether the Wnt/β-catenin signaling pathway was involved in the osteogenic differentiation of paeoniflorin. Osteoclastogenesis in RAW264.7 cells was identified by tartrate-resistant acid phosphatase (TRAP) staining.

Results: At concentrations ranging from 0.1 to 100 μM, paeoniflorin was not cytotoxic to MC3T3-E1 cells. Paeoniflorin significantly increased the osteogenic differentiation of MC3T3-E1 cells in a dose-dependent manner. Moreover, paeoniflorin significantly increased osteogenic differentiation gene and protein expression. Through bioinformatic analysis, paeoniflorin-affected genes were found to be involved in different signaling pathways, such as the Wnt/β-catenin signaling pathway. Paeoniflorin enhanced β-catenin and CyclinD1 expression compared with that of the control groups. DKK-1 partially reversed the promoting effects of paeoniflorin in promoting osteogenic differentiation of MC3T3-E1 cells. Moreover, paeoniflorin inhibited the osteoclastogenesis of RAW264.7 cells.

Conclusion: Paeoniflorin promotes osteogenic differentiation in MC3T3-E1 cells by regulating the Wnt/β-catenin pathway. Paeoniflorin is a potential therapeutic agent for the treatment of osteoporosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842535PMC
http://dx.doi.org/10.1186/s13018-022-02965-1DOI Listing

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