Phosphate promotes osteogenic differentiation through non-canonical Wnt signaling pathway in human mesenchymal stem cells.

Bone Pub Date : 2022-08-17 DOI:10.2139/ssrn.4145245
S. Rui, T. Kubota, Y. Ohata, Kenichi Yamamoto, M. Fujiwara, S. Takeyari, K. Ozono
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引用次数: 1

Abstract

BACKGROUND Phosphate is indispensable in osteogenesis and mineralization. However, mechanisms by which phosphate enhances osteogenic differentiation are not fully understood. In this study, we studied the effect of phosphate on osteogenic differentiation as well as signaling pathways induced by phosphate in the process. METHOD Induced human bone marrow-derived mesenchymal stem cells differentiation into osteoblasts by the change of media containing β-glycerophosphate (GP), 1 mM inorganic phosphate, or 3 mM inorganic phosphate (Pi). The differentiation of osteoblasts was verified by the expression of osteoblast differentiation markers and calcium deposition. RNA sequencing was performed to assess transcriptome in the early stage of osteogenic differentiation. RESULTS Osteogenic differentiation and mineralization were promoted in the 3 mM Pi group compared to those in the GP and 1 mM Pi groups on day 7 of culture. RNA sequencing revealed that the gene expressions involved in osteogenesis and the components in the Wnt signaling pathway was increased in 3 mM Pi group compared with those in the GP on day 7. Analysis with qPCR and Western blot suggested upregulation of components in the non-canonical Wnt signaling pathway, including WNT5b and phosphorylated-c-Jun in the 3 mM Pi group on day 7. WNT11 mRNA expression was increased in the 2 induction groups on day 7. Inhibition of WNT5b by siRNA experiment attenuated the components in non-canonical Wnt signaling expression, including WNT5b, WNT11 and ROR2 mRNA expression and phosphorylated-c-Jun protein expression. In addition, osteogenic differentiation and mineralization were partly decreased in 3 mM Pi group on day 7 by the inhibition of WNT5b. CONCLUSION Pi promoted osteogenic differentiation through the up-regulation of the non-canonical Wnt signaling pathway, including WNT5b, WNT11, p-c-Jun/c-Jun, in the early stage of differentiation. These findings provide a new perspective into the association of Pi and the non-canonical Wnt signaling pathway during osteogenic differentiation.
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磷酸盐通过非规范Wnt信号通路促进人间充质干细胞成骨分化。
磷酸盐在成骨和矿化中是不可缺少的。然而,磷酸盐促进成骨分化的机制尚不完全清楚。在本研究中,我们研究了磷酸盐对成骨分化的影响以及在此过程中磷酸盐诱导的信号通路。方法通过改变含有β-甘油磷酸(GP)、1 mM无机磷酸盐或3 mM无机磷酸盐(Pi)的培养基,诱导人骨髓间充质干细胞向成骨细胞分化。成骨细胞分化标志物的表达和钙沉积证实成骨细胞的分化。通过RNA测序来评估成骨分化早期的转录组。结果在培养第7天,与GP和1 mM Pi组相比,3 mM Pi组促进了成骨分化和矿化。RNA测序结果显示,与GP组相比,3 mM Pi组在第7天的成骨相关基因和Wnt信号通路组分的表达增加。qPCR和Western blot分析显示,3 mM Pi组在第7天上调了非规范Wnt信号通路中的成分,包括WNT5b和磷酸化c- jun。在第7天,2个诱导组的WNT11 mRNA表达均升高。siRNA实验抑制WNT5b后,WNT5b、WNT11、ROR2 mRNA表达和磷酸化c- jun蛋白表达等非规范Wnt信号表达组分减弱。此外,3 mM Pi组在第7天通过抑制WNT5b部分抑制成骨分化和矿化。结论pi在分化早期通过上调WNT5b、WNT11、p-c-Jun/c-Jun等非规范Wnt信号通路促进成骨分化。这些发现为研究Pi与成骨分化过程中非规范Wnt信号通路的关联提供了新的视角。
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