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首页|期刊导航|河北医学|miR-613调控SphK1/S1P通路对IL-1β诱导的软骨细胞损伤的影响

miR-613调控SphK1/S1P通路对IL-1β诱导的软骨细胞损伤的影响

张佚舟 孙承军

河北医学2026,Vol.32Issue(4):542-549,8.
河北医学2026,Vol.32Issue(4):542-549,8.DOI:10.3969/j.issn.1006-6233.2026.04.03

miR-613调控SphK1/S1P通路对IL-1β诱导的软骨细胞损伤的影响

The Effect of miR-613 on IL-1β-Induced Chondrocyte Injury by Regulating the SphK1/S1P Pathway

张佚舟 1孙承军2

作者信息

  • 1. 武汉科技大学附属华润武钢总医院骨科,湖北 武汉 430080||武汉科技大学医学院医学部,湖北 武汉 430080
  • 2. 武汉科技大学附属华润武钢总医院骨科,湖北 武汉 430080
  • 折叠

摘要

Abstract

Objective:To explore the effect of microRNA-613(miR-613)on interleukin-1β(IL-1β)-induced chondrocyte injury by regulating the sphingosine kinase 1(SphK1)/sphingosine 1-phosphate(S1P)pathway.Methods:Dual luciferase reporter gene assay was used to detect the interaction between miR-613 and SphK1.CHON-001 cells were divided into six groups:Ctrl group(normal culture),IL-1β group(10ng/mL IL-1β induction),NC-mimics group(NC-mimics transfection+IL-1β induction),miR-613-mimics group(miR-613-mimics transfection+IL-1β induction),miR-613-mimics+OE-NC group(miR-613-mimics+OE-NC co-transfection+IL-1β induction),and miR-613-mimics+OE-SphK1 group(miR-613-mimics+OE-SphK1 co-transfection+IL-1β induction).QRT-PCR was used to detect the expression of miR-613,SphK1,and S1P mRNA in CHON-001 cells.MTT and EdU staining were used to measure CHON-001 cell proliferation.Flow cytometry and TUNEL staining were performed to measure CHON-001 cell apopto-sis.An ELISA kit was used to measure the expression of IL-6 and TNF-α in CHON-001 cells.Moreover,a Western blot was performed to detect the expression of SphK1,S1P,MMP-13,and ADAMTS-5 proteins in CHON-001 cells.Results:MiR-613 could target the negative regulation of SphK1.Compared to the Ctrl group,the IL-1β group showed decreased EdU-positive cell rate,OD570 value,and miR-613 expression,while apoptosis rate,levels of IL-6,TNF-α,SphK1 mRNA and protein,S1P mRNA and protein,MMP-13,and ADAMTS-5 were increased(P<0.05).Compared to the IL-1β group and the NC-mimics group,the miR-613-mimics group exhibited increased EdU-positive cell rate,OD570 value,and miR-613 expression,whereas the apoptosis rate,levels of IL-6,TNF-α,SphK1 mRNA and protein,S1P mRNA and protein,MMP-13,and ADAMTS-5 were decreased(P<0.05).Compared to the miR-613-mimics group and the miR-613-mimics+OE-NC group,the miR-613-mimics+OE-SphK1 group had decreased EdU-positive cell rate and OD570 value,while apoptosis rate,levels of IL-6,TNF-α,SphK1 mRNA and protein,S1P mRNA and pro-tein,MMP-13,and ADAMTS-5 were increased(P<0.05).Conclusion:MiR-613 may inhibit IL-1β-in-duced chondrocyte injury by suppressing the SphK1/S1P pathway.

关键词

软骨细胞损伤/微小RNA-613/鞘氨醇激酶1/鞘氨醇-1-磷酸/白细胞介素-1β

Key words

Chondrocyte injury/MicroRNA-613/Sphingosine kinase 1/Sphingosine-1-phos-phate/Interleukin-1β

引用本文复制引用

张佚舟,孙承军..miR-613调控SphK1/S1P通路对IL-1β诱导的软骨细胞损伤的影响[J].河北医学,2026,32(4):542-549,8.

基金项目

湖北省武汉市医学科研项目,(编号:WX21D83) (编号:WX21D83)

河北医学

1006-6233

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