首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Interleukin-1 alpha alters the expression of matrix metalloproteinases and collagen degradation by pulp fibroblasts.
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Interleukin-1 alpha alters the expression of matrix metalloproteinases and collagen degradation by pulp fibroblasts.

机译:白细胞介素-1α改变纸浆成纤维细胞基质金属蛋白酶的表达和胶原降解。

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摘要

Matrix metalloproteinases (MMPs) and the tissue inhibitors of MMPs (TIMPs) have been suggested to play a role in dental pulp destruction. This study examined the effects of interleukin (IL)-1 alpha on pulp fibroblasts. The ability of these cells to degrade collagen was determined with or without IL-1 alpha utilizing a cell-mediated collagen degradation assay. Reverse transcriptase-polymerase chain reaction was utilized to examine the mRNA expression of multiple MMPs and TIMPs with and without IL-1 alpha, while Western blot analyses and zymography were utilized to examine their protein expression. The collagen degradation mediated by these cells was stimulated by IL-1 alpha and inhibited by MMP inhibitors. IL-1 alpha increased the mRNA expression of MMP-1 and MMP-3, as well as induced MMP-7. Western blot analyses confirmed these results. IL-1 alpha increased the secreted protein level of TIMP-1, while only slightly affected the level of TIMP-2. These results suggest that IL-1 alpha can induce pulp destruction by differentially regulating MMPs and TIMPs.
机译:基质金属蛋白酶(MMPs)和组织金属蛋白酶抑制剂(TIMPs)已被建议在牙髓破坏中发挥作用。这项研究检查了白细胞介素(IL)-1α对牙髓成纤维细胞的影响。利用细胞介导的胶原降解测定法,在有或没有IL-1α的情况下,测定这些细胞降解胶原的能力。逆转录酶-聚合酶链反应用于检测有或无IL-1 alpha的多种MMP和TIMP的mRNA表达,而蛋白质印迹分析和酶谱法则用于检测其蛋白表达。这些细胞介导的胶原蛋白降解被IL-1α刺激,并被MMP抑制剂抑制。 IL-1α增加MMP-1和MMP-3的mRNA表达,以及诱导的MMP-7。蛋白质印迹分析证实了这些结果。 IL-1α增加了TIMP-1的分泌蛋白水平,而对TIMP-2的水平影响很小。这些结果表明,IL-1α可通过差异调节MMP和TIMP诱导果肉破坏。

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