Development of Muscle Tendon Junction in vitro Using Aligned Electrospun PCL Fibres

Q1 Medicine Engineered regeneration Pub Date : 2024-01-24 DOI:10.1016/j.engreg.2024.01.004
Nodoka Iwasaki , Marta Roldo , Aikaterina Karali , Alberto Sensini , Gordon Blunn
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Abstract

The muscle tendon junction (MTJ) transmits the force generated by the muscle to the tendon and ultimately to the bone. Tears and strains commonly occur at the MTJ where regeneration is limited due poor vascularisation and the complexity of the tissue. Currently treatments for a complete MTJ tear are often unsuccessful. The creation of a tissue engineered MTJ would therefore be beneficial in the development of a novel treatment. In this study, aligned electrospun polycaprolactone fibres were fabricated and human myoblasts and tenocytes were cultured on the scaffold. The effect of 10 % cyclic strain and co-culture of myoblasts and tenocytes on the MTJ formation was investigated. The application of strain significantly increased cell elongation, and MTJ marker gene expression. Co-culture of myoblasts and tenocytes with strain induced higher MTJ marker gene expression compared with myoblasts and tenocytes cultured separately. Paxillin and collagen 22, naturally found in the MTJ, were also produced when cells were combined and grown in a 10 % strain environment. For the first time these results showed that the combination of the strain and co-culture of myoblasts and tenocytes promotes gene expression and production of proteins that are found in the MTJ.

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利用对齐的电纺 PCL 纤维体外开发肌肉肌腱接合处
肌肉肌腱连接处(MTJ)将肌肉产生的力量传递到肌腱,并最终传递到骨骼。撕裂和拉伤通常发生在MTJ处,由于血管不发达和组织复杂,再生受到限制。目前,针对 MTJ 完全撕裂的治疗往往不成功。因此,制造一种组织工程化的 MTJ 将有利于开发一种新的治疗方法。本研究制造了排列整齐的电纺聚己内酯纤维,并在支架上培养了人类成肌细胞和腱细胞。研究了 10% 循环应变以及成肌细胞和腱细胞共同培养对 MTJ 形成的影响。施加应变明显增加了细胞伸长和 MTJ 标记基因的表达。与单独培养的成肌细胞和腱细胞相比,应变与成肌细胞和腱细胞共同培养可诱导更高的 MTJ 标记基因表达。当细胞结合并在10%的应变环境中生长时,MTJ中天然存在的Paxillin和胶原蛋白22也会产生。这些结果首次表明,结合菌株并共同培养肌母细胞和腱细胞可促进 MTJ 中的基因表达和蛋白质的产生。
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来源期刊
Engineered regeneration
Engineered regeneration Biomaterials, Medicine and Dentistry (General), Biotechnology, Biomedical Engineering
CiteScore
22.90
自引率
0.00%
发文量
0
审稿时长
33 days
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