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白细胞介素-20 通过 GSK3β/β-catenin 信号通路抑制 MC3T3-E1 细胞的成骨分化。

Interleukin-20 inhibits the osteogenic differentiation of MC3T3-E1 cells via the GSK3β/β-catenin signalling pathway.

机构信息

Hospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, China; Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.

Hospital of Stomatology, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, China; Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.

出版信息

Arch Oral Biol. 2021 May;125:105111. doi: 10.1016/j.archoralbio.2021.105111. Epub 2021 Mar 22.

DOI:10.1016/j.archoralbio.2021.105111
PMID:33798924
Abstract

OBJECTIVE

To investigate the effects of interleukin-20 (IL-20) on the osteogenic differentiation of MC3T3-E1 cells.

METHODS

The pre-osteoblast line MC3T3-E1 was treated with different concentrations of IL-20 (0, 2, 20 and 100 ng/mL), and the cell viability was detected by the CCK8 assay. To assess the influence of IL-20 on osteogenic differentiation, alkaline phosphatase (ALP) activity and Alizarin red staining were performed at predetermined times. The expression levels of Runt-related transcription factor 2 (RUNX2), Osterix (Osx), glycogen synthase kinase-3β (GSK-3β) and β-catenin were detected by qRT-PCR and Western blotting analyses. 5 nmol/L lithium chloride (LiCl) was used as GSK-3β inhibitor.

RESULTS

IL-20 promoted cell proliferation but decreased ALP activity and mineralization. Moreover, IL-20 downregulated the expression of RUNX2, Osx and β-catenin but upregulated the level of GSK-3β.

CONCLUSIONS

The results suggest that IL-20 could inhibit the osteogenic differentiation of MC3T3-E1 cells via the GSK3β/β-catenin signalling pathway.

摘要

目的

研究白细胞介素-20(IL-20)对 MC3T3-E1 细胞成骨分化的影响。

方法

用不同浓度的白细胞介素-20(0、2、20 和 100ng/ml)处理前成骨细胞系 MC3T3-E1,用 CCK8 法检测细胞活力。为了评估 IL-20 对成骨分化的影响,在预定时间进行碱性磷酸酶(ALP)活性和茜素红染色。通过 qRT-PCR 和 Western blot 分析检测 runt 相关转录因子 2(RUNX2)、osterix(Osx)、糖原合成酶激酶-3β(GSK-3β)和β-连环蛋白的表达水平。用 5nmol/L 氯化锂(LiCl)作为 GSK-3β 抑制剂。

结果

IL-20 促进细胞增殖,但降低 ALP 活性和矿化。此外,IL-20 下调 RUNX2、Osx 和 β-连环蛋白的表达,但上调 GSK-3β 的水平。

结论

结果表明,IL-20 可通过 GSK3β/β-连环蛋白信号通路抑制 MC3T3-E1 细胞的成骨分化。

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