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首页> 外文期刊>Connective tissue research >Antisense Oligonucleotides Reduce Synthesis of Procollagen alpha1 (V) Chain in Human Patellar Tendon Fibroblasts: Potential Application in Healing Ligaments and Tendons.
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Antisense Oligonucleotides Reduce Synthesis of Procollagen alpha1 (V) Chain in Human Patellar Tendon Fibroblasts: Potential Application in Healing Ligaments and Tendons.

机译:反义寡核苷酸减少人类Pat骨肌腱成纤维细胞中原胶原α1(V)链的合成:在修复韧带和肌腱中的潜在应用。

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摘要

Many ligaments and tendons will heal after injury. However, they heal with poor mechanical properties when compared with the native tissue and show no improvement of these properties with time. Although the mechanisms that lead to this process are poorly understood, the presence of uniformly smaller collagen fibrils is believed to play a major role. Quantitatively minor when compared with type I collagen, type V collagen was found to be significantly elevated in healing medial collateral ligament of the rabbit knee. Previous studies have shown that type V collagen plays a role in regulating the diameter of type I collagen fibrils and reducing its level may lead to the formation of larger collagen fibrils in healing ligaments. Hence, type V collagen antisense gene therapy may be an approach to obtain this goal. In this study, our objective was to find specific antisense oligonucleotide sequences for type V procollagen alpha1 chain to elucidate the feasibility of type V collagen antisense gene therapy inligaments or tendons. We hypothesized that antisense oligonucleotides that selectively target the type V procollagen alpha1 chain mRNA could partially reduce the synthesis of type V procollagen alpha1 chain in human tendon fibroblasts. Western blotting analysis showed that antisense oligonucleotides (AS-V1 and AS-V2) significantly reduced synthesis of type V procollagen alpha1 chain. In addition, reverse transcription polymerase chain reaction revealed that both antisense oligonucleotides partially reduced type V procollagen alpha1 chain mRNA expression. This experiment identified two sequences within the type V procollagen coding region that are susceptible to antisense suppression, and thus provide the basis to explore the effects of antisense oligonucleotides on type V collagen synthesis, collagen fibril diameter, and mechanical properties of healing tendons and ligaments.
机译:许多韧带和肌腱在受伤后会he愈。但是,与天然组织相比,它们具有较差的机械性能,并且随着时间的推移这些性能没有改善。尽管对导致该过程的机理了解甚少,但据信均匀较小的胶原蛋白原纤维的存在起着主要作用。与I型胶原相比,V型胶原在兔子膝关节内侧副韧带的愈合中明显增高。先前的研究表明,V型胶原蛋白在调节I型胶原蛋白原纤维的直径中起作用,降低其水平可能导致愈合韧带中形成较大的胶原蛋白原纤维。因此,V型胶原反义基因治疗可能是实现这一目标的一种方法。在这项研究中,我们的目标是找到V型胶原蛋白原α1链的特定反义寡核苷酸序列,以阐明V型胶原蛋白反义基因治疗物或肌腱的可行性。我们假设选择性地靶向V型胶原蛋白α1链mRNA的反义寡核苷酸可以部分减少人肌腱成纤维细胞中V型胶原蛋白α1链的合成。蛋白质印迹分析表明,反义寡核苷酸(AS-V1和AS-V2)显着减少了V型胶原蛋白原α1链的合成。此外,逆转录聚合酶链反应显示,这两个反义寡核苷酸均部分降低了V型胶原原α1链的mRNA表达。该实验在V型原胶原编码区域内鉴定了两个易于反义抑制的序列,从而为探索反义寡核苷酸对V型胶原合成,胶原原纤维直径以及愈合肌腱和韧带的机械性能的影响提供了基础。

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