Department of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, 20129 Milano, Italy.
Department of Pharmaceutical Sciences, Università degli Studi di Milano, 20133 Milano, Italy.
Int J Mol Sci. 2020 Jun 30;21(13):4661. doi: 10.3390/ijms21134661.
Bone remodeling and repair require osteogenic cells to reach the sites that need to be rebuilt, indicating that stimulation of osteoblast migration could be a promising osteoanabolic strategy. We showed that purified δ-tocotrienol (δ-TT, 10 μg/mL), isolated from commercial palm oil () fraction, stimulates the migration of both MC3T3-E1 osteoblast-like cells and primary human bone marrow mesenchymal stem cells (BMSC) as detected by wound healing assay or Boyden chamber assay respectively. The ability of δ-TT to promote MC3T3-E1 cells migration is dependent on Akt phosphorylation detected by Western blotting and involves Wnt/β-catenin signalling pathway activation. In fact, δ-TT increased β-catenin transcriptional activity, measured using a Nano luciferase assay and pretreatment with procaine (2 µM), an inhibitor of the Wnt/β-catenin signalling pathway, reducing the wound healing activity of δ-TT on MC3T3-E1 cells. Moreover, δ-TT treatment increased the expression of β-catenin specific target genes, such as Osteocalcin and Bone Morphogenetic Protein-2, involved in osteoblast differentiation and migration, and increased alkaline phosphatase and collagen content, osteoblast differentiation markers. The ability of δ-TT to enhance the recruitment of BMSC, and to promote MC3T3-E1 differentiation and migratory behavior, indicates that δ-TT could be considered a promising natural anabolic compound.
骨骼重塑和修复需要成骨细胞到达需要重建的部位,这表明刺激成骨细胞迁移可能是一种很有前途的促合成代谢策略。我们表明,从商业棕榈油()馏分中分离出的纯化 δ-生育三烯酚(δ-TT,10μg/ml),分别通过划痕愈合试验或 Boyden 室试验检测,可刺激 MC3T3-E1 成骨样细胞和原代人骨髓间充质干细胞(BMSC)的迁移。δ-TT 促进 MC3T3-E1 细胞迁移的能力依赖于 Western blot 检测到的 Akt 磷酸化,并涉及 Wnt/β-catenin 信号通路的激活。事实上,δ-TT 增加了使用 Nano luciferase 测定法测量的β-连环蛋白转录活性,并且用普鲁卡因(2µM)预处理,Wnt/β-catenin 信号通路的抑制剂,降低了 δ-TT 对 MC3T3-E1 细胞的愈合活性。此外,δ-TT 处理增加了β-连环蛋白特异性靶基因的表达,例如骨钙素和骨形态发生蛋白-2,参与成骨细胞分化和迁移,并增加碱性磷酸酶和胶原蛋白含量,成骨细胞分化标志物。δ-TT 增强 BMSC 募集以及促进 MC3T3-E1 分化和迁移行为的能力表明,δ-TT 可以被认为是一种很有前途的天然合成代谢化合物。