2012Journal of Tongji UniversityRequires access

Effects of low density lipoproteins on mouse osteoblast

Lei Tao

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Abstract

Objective To investigate the effect of low density lipoprotein(LDL) on the proliferation and differentiation of mouse osteoblasts and related mechanism.Methods Mouse osteoblasts MC3T3-E1 were cultured with low density lipoprotein(LDL) at concentration of 0.05,0.1 and 0.2 mg/ml,respectively.The proliferation and differentiation of MC3T3-E1osteoblasts were detected with CCK-8 after treated with LDL for 24,48 and 72h.The osteocalcin levels were detected by ELISA and the expression of LDL receptor-related protein 5(LRP5) and dickkopf-1(DKK1),were detected by real-time PCR.Results The proliferation of osteoblasts was significantly suppressed by LDL treatment in a dose-and time-dependence manner(P0.05).ELISA showed that osteocalcin expression was inhibited by LDL with a dose-and time-dependence manner(P0.05).Real-Time PCR results exhibited that expression of LRP5 mRNA was up-regulated and expression of DKK1 mRNA was down-regulated with 0.05 mg/ml LDL for 48h(P0.05).Conclusion LDL can suppress the proliferation and differentiation of osteoblasts,which might be correlated with the up-regulation of LRP5 gene and down-regulation of its antagonist DKK1 gene in the wnt signal passageway.

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Objective To investigate the effect of low density lipoprotein(LDL) on the proliferation and differentiation of mouse osteoblasts and related mechanism.Methods Mouse osteoblasts MC3T3-E1 were cultured with low density lipoprotein(LDL) at concentration of 0.05,0.1 and 0.2 mg/ml,respectively.The proliferation and differentiation of MC3T3-E1osteoblasts were detected with CCK-8 after treated with LDL for 24,48 and 72h.The osteocalcin levels were detected by ELISA and the expression of LDL receptor-related protein 5(LRP5) and dickkopf-1(DKK1),were detected by real-time PCR.Results The proliferation of osteoblasts was significantly suppressed by LDL treatment in a dose-and time-dependence manner(P0.05).ELISA showed that osteocalcin expression was inhibited by LDL with a dose-and time-dependence manner(P0.05).Real-Time PCR results exhibited that expression of LRP5 mRNA was up-regulated and expression of DKK1 mRNA was down-regulated with 0.05 mg/ml LDL for 48h(P0.05).Conclusion LDL can suppress the proliferation and differentiation of osteoblasts,which might be correlated with the up-regulation of LRP5 gene and down-regulation of its antagonist DKK1 gene in the wnt signal passageway.

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Available abstract

Objective To investigate the effect of low density lipoprotein(LDL) on the proliferation and differentiation of mouse osteoblasts and related mechanism.Methods Mouse osteoblasts MC3T3-E1 were cultured with low density lipoprotein(LDL) at concentration of 0.05,0.1 and 0.2 mg/ml,respectively.The proliferation and differentiation of MC3T3-E1osteoblasts were detected with CCK-8 after treated with LDL for 24,48 and 72h.The osteocalcin levels were detected by ELISA and the expression of LDL receptor-related protein 5(LRP5) and dickkopf-1(DKK1),were detected by real-time PCR.Results The proliferation of osteoblasts was significantly suppressed by LDL treatment in a dose-and time-dependence manner(P0.05).ELISA showed that osteocalcin expression was inhibited by LDL with a dose-and time-dependence manner(P0.05).Real-Time PCR results exhibited that expression of LRP5 mRNA was up-regulated and expression of DKK1 mRNA was down-regulated with 0.05 mg/ml LDL for 48h(P0.05).Conclusion LDL can suppress the proliferation and differentiation of osteoblasts,which might be correlated with the up-regulation of LRP5 gene and down-regulation of its antagonist DKK1 gene in the wnt signal passageway.

Key concepts: DKK1, Osteocalcin, Chemistry, Osteoblast, LDL receptor, LRP5, Endocrinology, Messenger RNA

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