首页> 外文期刊>Journal of cellular and molecular medicine. >Effect of cyclic tensile load on the regulation of the expression of matrix metalloproteases (MMPs -1, -3) and structural components in synovial cells.
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Effect of cyclic tensile load on the regulation of the expression of matrix metalloproteases (MMPs -1, -3) and structural components in synovial cells.

机译:周期性拉伸负荷对滑膜细胞中基质金属蛋白酶(MMP -1,-3)和结构成分表达的调节。

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摘要

Synovial cells are reported to colonize synthetic ligament scaffolds following anterior cruciate ligament (ACL) reconstruction but the process leading to ligamentization is poorly understood. The present study investigated the effect of cyclic tensile strain on the expression of genes involved in matrix remodelling in bovine synovial cells seeded onto an artificial ligament scaffold. Synovial cells were seeded and cultured on polyester scaffolds for 3 weeks and subsequently subjected to cyclic tensile strain of 4.5% for 1 hr at frequency of 1 Hz. Changes in the levels of expression of genes for major ligament components (type I and type III collagen) and also metalloproteinases (MMP-1 and MMP-3), and TIMP-1 were examined using RT-PCR. Additionally, metalloproteinase activity was measured using both zymography and collagenase assays. The gene expression of MMP-3 transcripts in the loaded group was almost 3-fold that observed in control group but no differences were observed in other transcripts. Consistent with these findings, MMP-3 activity increased by 85% under mechanical stimulus, and MMP-1 activity showed no changes. Over expression of MMP-3 under cyclic tensile load may mediate the proteolysis of certain substrates surrounding the ligament scaffold. This will play a critical role in facilitating cell migration, proliferation and tissue remodelling by breaking down the provisional tissue formed by the synovium, and by generating factors that induce angiogenesis and chemotactic cell migration.
机译:据报道,滑膜细胞在前交叉韧带(ACL)重建后定居在合成韧带支架上,但导致韧带化的过程了解甚少。本研究调查了循环拉伸应变对植入人工韧带支架上的牛滑膜细胞中参与基质重塑的基因表达的影响。将滑膜细胞播种并在聚酯支架上培养3周,然后以1 Hz的频率经受4.5%的循环拉伸应变1小时。使用RT-PCR检测主要韧带成分(I型和III型胶原)以及金属蛋白酶(MMP-1和MMP-3)和TIMP-1的基因表达水平的变化。另外,使用酶谱法和胶原酶测定法测量金属蛋白酶活性。负荷组中MMP-3转录本的基因表达几乎是对照组的3倍,而其他转录本没有差异。与这些发现一致,在机械刺激下,MMP-3活性增加了85%,而MMP-1活性没有变化。 MMP-3在循环拉伸载荷下的过表达可能介导韧带支架周围某些底物的蛋白水解。这将通过破坏滑膜形成的临时组织,并产生诱导血管生成和趋化性细胞迁移的因子,在促进细胞迁移,增殖和组织重塑中起关键作用。

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