Curcumin Inhibits Lipopolysaccharide-Induced Inflammation Through the HMGB1/NF-κB Signaling Pathway to Promote the Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jimei Zhang, Donggang Mou, Ling Zhu, Jianping Zhou, Qunying Yu, Guangyuan Yang, Chaoli Luo, Jianguo Meng, Kewang Mao, Jing Liu, Bo Yan, Xuming Yang
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Abstract

Curcumin has strong anti-inflammatory properties and promotes the osteogenic differentiation of human bone marrow mesenchymal stem cells (hBMSCs). The aim of this study was to explore the role and potential molecular mechanism of curcumin in ameliorating osteogenic differentiation disorders caused by inflammation. We used LPS to induce an inflammatory response in hBMSCs. The expression of related mRNAs and proteins was detected by RT‒qPCR, Western blotting, immunofluorescence, and ELISA. The osteogenic differentiation of hBMSCs was detected by alkaline phosphatase (ALP) staining and alizarin red S (ARS) staining. The results showed that after LPS treatment, the levels of the inflammatory cytokines TNF-α, IL-6 and IL-1β in hBMSCs increased, and the activity of ALP, the level of calcium salt deposition and the expression levels of the osteogenic proteins Runx2, COL1, OCN and OPN significantly decreased. The curcumin treatment alleviated this effect. These results indicated that curcumin improved the LPS-induced inflammation and osteogenic differentiation disorder in hBMSCs. Further studies revealed that the therapeutic effect of curcumin was caused by the inhibition of HMGB1 expression. From a mechanistic perspective, curcumin inhibits LPS-induced inflammation by inhibiting the expression of HMGB1, thereby inhibiting the NF-κB pathway and activating the NRF2 pathway, thereby improving the disordered osteogenic differentiation of hBMSCs. In conclusion, curcumin can reduce the LPS-induced inflammation of hBMSCs and ameliorate their osteogenic differentiation disorders.

姜黄素通过HMGB1/NF-κB信号通路抑制脂多糖诱导炎症促进骨髓间充质干细胞成骨分化
姜黄素具有很强的抗炎作用,能促进人骨髓间充质干细胞(hBMSCs)的成骨分化。本研究旨在探讨姜黄素在改善炎症引起的成骨分化障碍中的作用及其可能的分子机制。我们使用LPS诱导hBMSCs的炎症反应。RT-qPCR、Western blotting、免疫荧光和ELISA检测相关mrna和蛋白的表达。碱性磷酸酶(ALP)染色和茜素红S (ARS)染色检测骨髓间充质干细胞成骨分化。结果显示,LPS处理后,hBMSCs中炎症因子TNF-α、IL-6、IL-1β水平升高,ALP活性、钙盐沉积水平及成骨蛋白Runx2、COL1、OCN、OPN表达水平显著降低。姜黄素治疗减轻了这种作用。结果表明,姜黄素可改善脂多糖诱导的hBMSCs炎症和成骨分化障碍。进一步研究发现姜黄素的治疗作用是通过抑制HMGB1的表达引起的。从机制上看,姜黄素通过抑制HMGB1的表达抑制lps诱导的炎症,从而抑制NF-κB通路,激活NRF2通路,从而改善hBMSCs的成骨分化紊乱。综上所述,姜黄素可以减轻脂多糖诱导的hBMSCs炎症,改善其成骨分化障碍。
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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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