...
首页> 外文期刊>Rheumatology International >Activin A suppresses interleukin-1-induced matrix metalloproteinase 3 secretion in human chondrosarcoma cells
【24h】

Activin A suppresses interleukin-1-induced matrix metalloproteinase 3 secretion in human chondrosarcoma cells

机译:激活素A抑制人软骨肉瘤细胞中白介素1诱导的基质金属蛋白酶3分泌

获取原文
获取原文并翻译 | 示例
           

摘要

The objective was to investigate the effect of activin A on matrix metalloproteinase 3 (MMP-3) production and to identify the role of activin A in chondroprotection. SW1353 cells, a human chondrosarcoma cell line, were stimulated with interleukin (IL) 1α and tumor necrosis factor (TNF) α, and the concentrations of activin A, follistatin, and MMP-3 secreted into the culture media were measured by enzyme-linked immunosorbent assay (ELISA). Activin A was added to cell cultures in the presence of IL-1α or TNFα to determine its effect on the production of MMP-3 and sulfated glycosaminoglycan (sGAG) (measured by Alcian blue assay). To study the mechanism responsible for the chondroprotective effects of activin A, the production of IL-1 receptor antagonist (IL-1ra) and tissue inhibitor for metalloproteinases 1 (TIMP-1) was examined by ELISA. Addition of IL-1α did not affect the production of activin A by cultured SW1353 cells. IL-1α and activin A inhibited the production of follistatin. Stimulation of SW1353 cells with activin A suppressed IL-1α-induced, but not TNFα-induced, MMP-3 expression. Activin A had no effect on the production of sGAG, IL-1ra, or TIMP-1, although it suppressed the induction of TIMP-1 and IL-1ra by IL-1α. This novel finding of MMP-3 inhibition by activin A suggests a new role of activin A in cartilage remodeling. Activin A may have therapeutic potential for preventing cartilage degradation.
机译:目的是研究激活素A对基质金属蛋白酶3(MMP-3)产生的影响,并确定激活素A在软骨保护中的作用。用白细胞介素(IL)1α和肿瘤坏死因子(TNF)α刺激人软骨肉瘤细胞系SW1353细胞,并通过酶联法测定分泌到培养基中的激活素A,卵泡抑素和MMP-3的浓度。免疫吸附测定(ELISA)。在IL-1α或TNFα存在的情况下,将激活素A添加到细胞培养物中,以确定其对MMP-3和硫酸化糖胺聚糖(sGAG)产生的影响(通过阿尔辛蓝测定法测量)。为了研究激活素A的软骨保护作用的机制,通过ELISA检测了IL-1受体拮抗剂(IL-1ra)和金属蛋白酶1组织抑制剂(TIMP-1)的产生。 IL-1α的添加不影响培养的SW1353细胞产生激活素A。 IL-1α和激活素A抑制卵泡抑素的产生。用激活素A刺激SW1353细胞可抑制IL-1α诱导的,但不能抑制TNFα诱导的MMP-3表达。激活素A对sGAG,IL-1ra或TIMP-1的产生没有影响,尽管它抑制了IL-1α对TIMP-1和IL-1ra的诱导。激活素A抑制MMP-3的这一新发现表明了激活素A在软骨重塑中的新作用。活化素A可能具有预防软骨降解的治疗潜力。

著录项

  • 来源
    《Rheumatology International》 |2007年第11期|1049-1055|共7页
  • 作者单位

    Department of Rheumatology Immunology and Allergy Tri-Service General Hospital National Defense Medical Center #325 Cheng-Kung Road Section 2 Neihu 114 Taipei Taiwan;

    Department of Rheumatology Immunology and Allergy Tri-Service General Hospital National Defense Medical Center #325 Cheng-Kung Road Section 2 Neihu 114 Taipei Taiwan;

    Department of Pathology Tri-Service General Hospital National Defense Medical Center Taipei Taiwan;

    Department of Rheumatology Immunology and Allergy Tri-Service General Hospital National Defense Medical Center #325 Cheng-Kung Road Section 2 Neihu 114 Taipei Taiwan;

    Department of Rheumatology Immunology and Allergy Tri-Service General Hospital National Defense Medical Center #325 Cheng-Kung Road Section 2 Neihu 114 Taipei Taiwan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Activin A; IL-1; Follistatin; Chondrocyte; MMP-3;

    机译:激活素A;IL-1;卵泡抑素;软骨细胞;MMP-3;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号