Butea monosperma bark extract: a natural boost for osteogenesis via Wnt/β-catenin pathway activation in adipose-derived mesenchymal stem cells

被引:0
作者
Sundar, Rebu [1 ,2 ]
Sundar, Gayathri [2 ,3 ]
John, Annie [1 ,2 ]
Abraham, Annie [3 ]
机构
[1] Univ Kerala, Adv Ctr Tissue Engn, Dept Biochem, Trivandrum 695581, Kerala, India
[2] Karunya Inst Technol & Sci, Ctr Res Mat Sci & Thermal Management CRMSTM, Coimbatore 641114, Tamil Nadu, India
[3] Univ Kerala, Dept Biochem, Trivandrum 695581, Kerala, India
关键词
Bone markers; Butea monosperma bark; Mesenchymal stem cells; Wnt/beta-catenin pathway; ANTIINFLAMMATORY ACTIVITY; SCAFFOLDS; DIFFERENTIATION; DELIVERY; DOCKING; ALPHA;
D O I
10.1007/s10529-024-03545-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
PurposeTo investigate the impact of Butea monosperma (BM) bark extract on the osteogenic differentiation potential of rat adipose-derived mesenchymal stem cells (rADMSCs) and to elucidate the involvement of Wnt/beta-catenin pathway in mediating this osseous effect.MethodsCharacterizations (antioxidant assays, FTIR and LC/MS analyses) and docking studies (in silico) were performed to evaluate the presence of phytochemicals in the BM extract and their binding capacity to that of the frizzled receptor. rADMSCs were isolated and characterised for its differentiation potential of osteogenesis for stemness. Dose fixation, cytotoxicity, osteogenic differentiation (calcium, mineral deposition, alkaline phosphatase and osteocalcin) and gene expression (osteocalcin, Col1, osteonectin, Bmp2, Runx2, Wnt2, and beta-catenin-14 and 28 days) of the extract were also evaluated in vitro.ResultsFTIR and LC/MS analyses unveiled the phytochemicals in the extract and with docking studies confirmed their interaction with the frizzled receptor of Wnt/beta-catenin pathway. rADMSCs were isolated and differentiated in the presence of the osteogenic induction medium. Dose fixation studies, cytotoxicity and cell viability assessments demonstrated the phytochemicals concentration-dependent cytotoxicity. The presence of specific bone markers highlighted the osteogenic differentiation potential of the phytochemicals. Furthermore, gene expression studies of rADMSCs depicted a heightened bone-forming capacity potentially facilitated by the activation of Wnt/beta-catenin pathway.Conclusion The phytochemicals of BM promoted the osteogenic differentiation of rADMSCs through the activation of the signalling Wnt/beta-Catenin pathway, as evidenced by the significant upregulation of early and late bone markers. The phytochemicals may therefore be positioned as promising therapeutic agents for enhancing bone regeneration, offering new avenues for regenerative medicine.
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页数:18
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