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白细胞介素-1对人关节软骨细胞和滑膜细胞中血管内皮生长因子及基质金属蛋白酶-3(基质溶解素)的诱导作用

Induction of vascular endothelial growth factor and matrix metalloproteinase-3 (stromelysin) by interleukin-1 in human articular chondrocytes and synoviocytes.

作者信息

Inoue Kenji, Masuko-Hongo Kayo, Okamoto Masahiro, Nishioka Kusuki

机构信息

Division of Molecular Regulation, Department of Bioregulation, Institute of Medical Science, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki-shi, Kanagawa 216-8512, Japan.

出版信息

Rheumatol Int. 2005 Dec;26(2):93-8. doi: 10.1007/s00296-004-0513-6. Epub 2004 Sep 29.

Abstract

We investigated the effects of interleukin (IL)-1 on vascular endothelial growth factor (VEGF) and matrix metalloproteinase-3 (MMP-3) (stromelysin) secretion from chondrocytes and synoviocytes in different clinical conditions. Specifically, cells obtained from osteoarthritic (OA) (n = 7), rheumatoid arthritic (RA) (n = 5), and post-traumatic (PT) (n = 5) patients were stimulated in vitro with IL-1beta in the presence or absence of an IL-1 receptor antagonist (IL-1ra) (anakinra). Levels of secreted MMP-3 and VEGF were measured by enzyme-linked immunosorbent assay. The VEGF mRNA expression was analyzed quantitatively. Interleukin-1 induced both VEGF and MMP-3 secretion from all of the samples tested, and VEGF mRNA expression was also upregulated. Interleukin-1ra significantly suppressed the enhancing effect of IL-1 on MMP-3 and VEGF in both cell types. In conclusion, IL-1 simultaneously induces MMP-3 and VEGF production from chondrocytes and synoviocytes in inflammatory, degenerative, and post-traumatic joints. Therefore, IL-1ra might be beneficial for protection from VEGF-mediated alterations of cartilage metabolism in pathologic and physiologic conditions.

摘要

我们研究了白细胞介素(IL)-1在不同临床情况下对软骨细胞和滑膜细胞分泌血管内皮生长因子(VEGF)和基质金属蛋白酶-3(MMP-3)(基质溶解素)的影响。具体而言,从骨关节炎(OA)患者(n = 7)、类风湿性关节炎(RA)患者(n = 5)和创伤后(PT)患者(n = 5)获取的细胞,在有或无IL-1受体拮抗剂(IL-1ra)(阿那白滞素)存在的情况下,用IL-1β进行体外刺激。通过酶联免疫吸附测定法测量分泌的MMP-3和VEGF水平。对VEGF mRNA表达进行定量分析。白细胞介素-1诱导了所有测试样本中VEGF和MMP-3的分泌,并且VEGF mRNA表达也上调。白细胞介素-1ra显著抑制了IL-1对两种细胞类型中MMP-3和VEGF的增强作用。总之,IL-1在炎症性、退行性和创伤后关节中同时诱导软骨细胞和滑膜细胞产生MMP-3和VEGF。因此,在病理和生理条件下,IL-1ra可能有助于防止VEGF介导的软骨代谢改变。

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