Interleukin-1α and Epidermal Growth Factor Synergistically Enhance the Release of Collagenase by Periosteal Connective Tissue In Vitro

Erwin Van Der Zee, Vincent Everts , Kees Hoeben, Wouter Beertsen
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引用次数: 19

Abstract

The effects of recombinant human interleukin-1α(IL-1α) and murine epidermal growth factor (EGF) on the release of collagenase were studied in an in vitro model system using periosteal explants from rabbit calvariae. Following an incubation period of 72 h it was shown that IL-1α in combination with EGF (IL-1α + EGF) induced a synergistic increase in the amount of collagenase released by periosteal explants. This increase appeared to be at least 10-fold. Most of the enzyme was present in a latent form since the increase in enzyme activity was only detectable after activation by APMA and the molecular weight as determined in immunoblots corresponded to the latent form of this enzyme. Incubations carried out with IL-1α alone resulted in a 2- to 4-fold increase of total enzyme activity, whereas the amount of collagenase in media of EGF-treated periostea did not surpass control values. A neutralizing anti-IL-1α antibody completely blocked the enhanced release of collagenase as induced both by IL-1α and by IL-1α + EGF. Indomethacin partially prevented the IL-1α + EGF-induced increase in enzyme release, suggesting the involvement of prostaglandins.

The amount of tissue inhibitor of metalloproteinases (TIMP) as determined by ELISA was slightly elevated in culture media obtained from all cytokine-treated explants. Comparable results were obtained by Western blot analysis as well as by a functional bioassay.

It is suggested that the concomitant presence of the cytokines IL-1α and EGF may play an important role in collagenase-mediated degradation of collagen.

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白细胞介素-1α和表皮生长因子协同促进骨周结缔组织胶原酶的释放
以兔颅骨骨膜为外植体,在体外模型系统中研究了重组人白细胞介素-1α(IL-1α)和鼠表皮生长因子(EGF)对胶原酶释放的影响。培养72小时后,显示IL-1α与EGF的组合(IL-1α+EGF)诱导骨膜外植体释放的胶原酶量协同增加。这一增长似乎至少是10倍。大多数酶以潜伏形式存在,因为酶活性的增加只有在APMA激活后才能检测到,并且在免疫印迹中测定的分子量对应于这种酶的潜伏形式。单独用IL-1α孵育导致总酶活性增加2-4倍,而EGF处理的骨膜培养基中胶原酶的量没有超过对照值。中和抗IL-1α抗体完全阻断了IL-1α和IL-1α+EGF诱导的胶原酶释放增强。吲哚美辛部分阻止了IL-1α+EGF诱导的酶释放增加,表明前列腺素参与其中。通过ELISA测定的金属蛋白酶组织抑制剂(TIMP)的量在从所有细胞因子处理的外植体获得的培养基中略有升高。通过蛋白质印迹分析以及功能生物测定获得了可比较的结果。提示细胞因子IL-1α和EGF的同时存在可能在胶原酶介导的胶原降解中发挥重要作用。
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