TGF-β/Smad/ADAMTS-7 Axis Regulates the Process of Curcumin in Promoting the Cartilage Cells Proliferation

IF 0.4 4区 医学 Q4 PHARMACOLOGY & PHARMACY Indian Journal of Pharmaceutical Sciences Pub Date : 2023-01-01 DOI:10.36468/pharmaceutical-sciences.1151
X. B. Niu, Jiangying Zhang, Y. C. Wang, Lei Guo, Y. X. Liu, W. Liu, XU Y.S.
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Abstract

To explore the function of curcumin on the cartilage cells, the cell proliferation and apoptosis by transforming growth factor-beta/suppressor of mothers against decapentaplegic/a disintegrin and metalloproteinase with thrombospondin motifs-7 axis was the objective of the study. The cell viability was detected by cell counting kit-8. The expression of transforming growth factor-beta, suppressor of mothers against decapentaplegic protein, a disintegrin and metalloproteinase with thrombospondin motifs-7, caspase-9, B-cell lymphoma 2, Bcl-2-associated X protein was determined by Western blot. The cartilage cells were treated with 1 mmol/l sodium nitroprusside for 24 h. Then, the cells were treated with different concentration of curcumin for 24 h. We found that 1 μmol/l curcumin could recover the cartilage cells proliferation. The transforming growth factor-beta and suppressor of mothers against decapentaplegic protein show high expression and a disintegrin and metalloproteinase with thrombospondin motifs-7 was low in the curcumin treatment group. Meanwhile, the apoptosis pathway was also detected. The caspase-9 and B-cell lymphoma 2 was higher in the curcumin treatment group than without curcumin group. However, the Bcl-2-associated X protein was lower. The cell viability, a disintegrin and metalloproteinase with thrombospondin motifs-7, caspase-9, B-cell lymphoma 2 and Bcl-2-associated X proteins also show no changes with or without curcumin when the transforming growth factor-beta was inhibited. We found that a disintegrin and metalloproteinase with thrombospondin motifs-7 show over expression, the transforming growth factor-beta and suppressor of mothers against decapentaplegic protein show high expression in the curcumin treatment group, the cell viability, caspase-9, B-cell lymphoma 2 and Bcl-2-associated X proteins show no changes with or without curcumin. Curcumin can promote the cartilage cells proliferation via transforming growth factor-beta/suppressor of mothers against decapentaplegic/a disintegrin and metalloproteinase with thrombospondin motifs-7 axis and inhibit the cell apoptosis.
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TGF-β/Smad/ADAMTS-7轴调控姜黄素促进软骨细胞增殖的过程
本研究旨在探讨姜黄素通过转化生长因子- β /抑制因子抗十肢瘫痪/a崩解素和具有血小板反应蛋白-7轴的金属蛋白酶对软骨细胞增殖和凋亡的影响。采用细胞计数试剂盒-8检测细胞活力。Western blot检测转化生长因子- β、母亲抗十肢瘫痪蛋白抑制因子、具有血栓反应蛋白基序的崩解素和金属蛋白酶-7、caspase-9、b细胞淋巴瘤2、bcl -2相关X蛋白的表达。用1 mmol/l硝普钠处理软骨细胞24 h,然后用不同浓度的姜黄素处理24 h,发现1 μmol/l姜黄素能恢复软骨细胞的增殖。姜黄素治疗组转化生长因子- β和抗十足瘫痪蛋白抑制因子高表达,具有血栓反应蛋白基序的崩解素和金属蛋白酶-7低表达。同时检测细胞凋亡通路。姜黄素治疗组的caspase-9和b细胞淋巴瘤2高于未治疗组。而bcl -2相关的X蛋白则较低。当转化生长因子- β被抑制时,细胞活力、具有血栓反应蛋白基序-7、caspase-9、崩解素和金属蛋白酶、b细胞淋巴瘤2和bcl -2相关X蛋白也没有显示姜黄素或没有姜黄素的变化。我们发现,姜黄素治疗组的崩解素和具有血栓反应蛋白基序-7的金属蛋白酶呈高表达,转化生长因子- β和母亲抗十足瘫蛋白的抑制因子呈高表达,细胞活力、caspase-9、b细胞淋巴瘤2和bcl -2相关的X蛋白在姜黄素治疗组或不治疗组均无变化。姜黄素可通过转化生长因子- β /抗十肢瘫痪/a崩解素抑制因子和血小板反应蛋白-7轴金属蛋白酶促进软骨细胞增殖,抑制细胞凋亡。
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期刊介绍: The Indian Journal of Pharmaceutical Sciences (IJPS) is a bi-monthly Journal, which publishes original research work that contributes significantly to further the scientific knowledge in Pharmaceutical Sciences (Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy and Phytochemistry, Pharmacology and Therapeutics, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Pharmacovigilance, Pharmacoepidemiology, Pharmacoeconomics, Drug Information, Patient Counselling, Adverse Drug Reactions Monitoring, Medication Errors, Medication Optimization, Medication Therapy Management, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest). The Journal publishes original research work either as a Full Research Paper or as a Short Communication. Review Articles on current topics in Pharmaceutical Sciences are also considered for publication by the Journal.
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