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The effect of curcumin regulating the Notch1/Hes1/Prdx1 pathway on IL-1β-induced inflammatory injury of chondrocytes
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DOI   10.11656/j.issn.1672-1519.2026.06.12
Key Words   curcumin;Notch 1;hairy and enhancer of split homolog 1;peroxiredoxin 1;interleukin-1β;inflammatory injury
Author NameAffiliationE-mail
LU Zhaoping Dongguan Hospital of Guangzhou University of Chinese Medicine, Dongguan 523000, China  
HE Jiandong Dongguan Hospital of Guangzhou University of Chinese Medicine, Dongguan 523000, China  
TAN Zhichao Dongguan Hospital of Guangzhou University of Chinese Medicine, Dongguan 523000, China  
XIE Shangneng Dongguan Hospital of Guangzhou University of Chinese Medicine, Dongguan 523000, China xsnfine@163.com 
Abstract
    [Objective] To investigate the effect of curcumin(Cur)regulating the Notch1/hairy and enhancer of split homolog 1(Hes1)/ peroxiredoxin 1(Prdx1)pathway on inflammatory injury of chondrocytes induced by interleukin-1 β(IL-1β). [Methods] C28/I2 cells were randomly separated into Ctrl group(normal culture),IL-1β group(10 ng/mL IL-1β),low-dose Cur (L-CUR),medium-dose Cur (M- Cur),and high-dose Cur (H-Cur)groups(IL-1β induced+10,20,40 μmol/L Cur),and Cur+Jagged 1 group(IL-1β induced+40 μmol/L Cur+0.5 μg/mL Notch activator Jagged 1). The proliferation of C28/I2 cells was detected by MTS assay and 5-Ethynyl-2'-deoxyuridine (EdU)staining. The apoptosis of C28/I2 cells was detected by flow cytometry. The 2',7'-dichlorofluorescein diacetate(DCFH-DA) fluorescent probe was used to detect the level of reactive oxygen species(ROS)in C28/I2 cells. Immunofluorescence was used to detect the expressions of type Ⅱ collagen(ColⅡ)and Aggrecan in C28/I2 cells. Enzyme-linked immunosorbent assay(ELISA)kits were used to detect the expression of interleukin(IL)-6,IL-8,tumor necrosis factor-α(TNF-α),matrix metalloproteinase(MMP)-3,and MMP-13 in C28 / I2 cells. Western blot was used to detect the protein expression of proliferating cell nuclear antigen(Ki-67), minichromosome maintenance complex component 7(MCM)7,Notch1,Hes1,Prdx1,BCL2 antagonist(Bak),and survival protein (survivin)in C28 /I2 cells. [Results] The OD490 value,EdU positive cell rate,ColⅡ fluorescence intensity,Aggrecan fluorescence intensity,Ki-67,MCM7 and survivin in the IL-1β group were lower than those in the Ctrl group,while the apoptosis rate,ROS fluorescence,Bak,MMP-3,MMP-13,IL-6,IL-8,TNF-α,Notch1,Hes1 and Prdx1 were higher than those in the Ctrl group(P<0.05). The OD 490 value,EdU positive cell rate,ColⅡ fluorescence intensity,Aggrecan fluorescence intensity,Ki-67,MCM7 and survivin in the L-Cur group,M-Cur group,H-Cur group were higher than those in the IL-1β group,while the apoptosis rate,ROS fluorescence, Bak,MMP-3,MMP-13,IL-6,IL-8,TNF-α,Notch1,Hes1 and Prdx1 were lower than those in the IL-1β group(P<0.05). The OD490 value,EdU positive cell rate,ColⅡ fluorescence intensity,Aggrecan fluorescence intensity,Ki-67,MCM7 and survivin in the Cur+ Jagged 1 group were lower than those in the H-Cur group,while the apoptosis rate,ROS fluorescence,Bak,MMP-3,MMP-13,IL-6,IL-8, TNF-α,Notch1,Hes1 and Prdx1 were higher than those in the H-Cur group(P<0.05). [Conclusion] Cur alleviates IL-1β-induced inflammatory injury of chondrocytes by inhibiting the Notch1/Hes1/Prdx1 pathway.

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