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首页> 外文期刊>Biochimie >IL-17A suppresses the expression of bone resorption-related proteinases and osteoclast differentiation via IL-17RA or IL-17RC receptors in RAW264.7 cells
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IL-17A suppresses the expression of bone resorption-related proteinases and osteoclast differentiation via IL-17RA or IL-17RC receptors in RAW264.7 cells

机译:IL-17A通过RAW264.7细胞中的IL-17RA或IL-17RC受体抑制骨吸收相关蛋白酶的表达和破骨细胞分化

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摘要

Interleukin-17 (IL-17) is produced exclusively by activated T cells and neutrophils, and stimulates oste-oclastic bone resorption via osteoblasts by inducing the expression of "receptor activator of NF-κB (RANK) ligand" (RANKL). However, the direct effects of IL-17 on the differentiation of osteoclast precursors into osteoclasts and on the function of osteoclasts have not been clarified. Therefore, we examined the effects of IL-17A on the differentiation of osteoclast precursors using RAW264.7 cells and also on the expression of carbonic anhydrase Ⅱ (CA Ⅱ), cathepsin K, matrix metalloproteinases-9 (MMP-9), RANK, c-fms, and IL-17 receptors in these cells. The cells were cultured with or without 0.1,1.0,10 or 50 ng/mL IL-17 in the presence of soluble RANKL for up to 10 days. The CA Ⅱ, cathepsin K, and MMP-9 mRNA and protein expression levels were examined using real-time PCR and Western blotting, respectively. The mRNA expression levels of RANK, c-fms, and IL-17 receptors were monitored by realtime PCR. Osteoclast differentiation was estimated using tartrate-resistant acid phosphatase (TRAP) staining of the cells. TRAP-positive cells were observed after day 5 of culture, and the number of cells decreased in the presence of 10 and 50 ng/mL IL-17A at days 5 and 7. In the presence of IL-17A, the expressions of cathepsin K, MMP-9 and c-fms decreased markedly on days 5 and/or 7 of culture, whereas the expression of CA Ⅱ and IL-17 receptor (type A) increased remarkably at days 3 and 7, respectively. The expression of RANK and IL-17 receptor (type C) was not affected by the addition of IL-17A. These results suggest that the differentiation of osteoclast precursors into osteoclasts is suppressed at high concentrations of IL-17A. Furthermore, IL-17A suppresses the hydrolysis of matrix proteins during bone resorption by decreasing the production of cathepsin K and MMP-9 in osteoclasts.
机译:白细胞介素17(IL-17)仅由活化的T细胞和嗜中性粒细胞产生,并通过诱导“NF-κB(RANK)配体的受体激活剂”(RANKL)的表达,通过成骨细胞刺激破骨细胞吸收骨。然而,IL-17对破骨细胞前体分化为破骨细胞以及对破骨细胞功能的直接影响尚不清楚。因此,我们研究了IL-17A对RAW264.7细胞对破骨细胞前体细胞分化的影响,以及对碳酸酐酶Ⅱ(CAⅡ),组织蛋白酶K,基质金属蛋白酶9(MMP-9),RANK,这些细胞中的c-fms和IL-17受体。在可溶性RANKL存在下,在有或没有0.1、1.0、10或50 ng / mL IL-17的条件下培养细胞长达10天。分别采用实时荧光定量PCR和蛋白质印迹法检测CAⅡ,组织蛋白酶K和MMP-9的mRNA和蛋白表达水平。通过实时PCR监测RANK,c-fms和IL-17受体的mRNA表达水平。使用抗酒石酸的酸性磷酸酶(TRAP)染色估计破骨细胞的分化。培养第5天后观察到TRAP阳性细胞,在第5天和第7天存在10和50 ng / mL IL-17A时细胞数量减少。在IL-17A存在时,组织蛋白酶K的表达在培养的第5天和/或第7天,MMP-9和c-fms明显下降,而在第3天和第7天,CAⅡ和IL-17受体(A型)的表达显着增加。 IL-17A的加入不会影响RANK和IL-17受体(C型)的表达。这些结果表明,在高浓度的IL-17A下,破骨细胞前体向破骨细胞的分化受到抑制。此外,IL-17A通过减少破骨细胞中组织蛋白酶K和MMP-9的产生来抑制骨吸收过程中基质蛋白的水解。

著录项

  • 来源
    《Biochimie》 |2010年第4期|p.398-404|共7页
  • 作者单位

    Department of Oral Health Sciences, Nihon University School of Dentistry, 1-8-13, Kanda Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan;

    rnDepartment of Oral Health Sciences, Nihon University School of Dentistry, 1-8-13, Kanda Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan;

    rnDepartment of Oral Health Sciences, Nihon University School of Dentistry, 1-8-13, Kanda Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan Division of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan;

    rnDepartment of Oral Health Sciences, Nihon University School of Dentistry, 1-8-13, Kanda Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan Division of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan;

    rnDepartment of Oral Health Sciences, Nihon University School of Dentistry, 1-8-13, Kanda Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan;

    rnDepartment of Orthodontics, Shandong University School of Dentistry, Jinan, Shandong Province, China;

    rnDivision of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan Department of Biochemistry, Nihon University School of Dentistry, Tokyo, Japan;

    rnDepartment of Oral and Maxillofacial Surgery, Nihon University School of Dentistry, Tokyo, Japan Division of Systemic Biology and Oncology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan;

    rnDepartment of Oral Health Sciences, Nihon University School of Dentistry, 1-8-13, Kanda Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan Division of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    interleukin-17; osteoclast precursors; carbonic anhydrase Ⅱ; cathepsin K; matrix metalloproteinase-9;

    机译:白介素17;破骨细胞前体碳酸酐酶Ⅱ;组织蛋白酶K;基质金属蛋白酶9;

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