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驱动分层胶原纤维形成,用于功能性肌腱、韧带和半月板替代。

Driving Hierarchical Collagen Fiber Formation for Functional Tendon, Ligament, and Meniscus Replacement.

机构信息

Department of Materials, Department of Bioengineering, And Institute for Biomedical Engineering, Imperial College London, London, United Kingdom, SW7 2AZ; Department of Biomedical Engineering and Orthopaedic Surgery, Virginia Commonwealth University, Richmond, VA, United States, 23284.

Department of Materials, Department of Bioengineering, And Institute for Biomedical Engineering, Imperial College London, London, United Kingdom, SW7 2AZ.

出版信息

Biomaterials. 2021 Feb;269:120527. doi: 10.1016/j.biomaterials.2020.120527. Epub 2020 Nov 16.

Abstract

Hierarchical collagen fibers are the primary source of strength in musculoskeletal tendons, ligaments, and menisci. It has remained a challenge to develop these large fibers in engineered replacements or in vivo after injury. The objective of this study was to investigate the ability of restrained cell-seeded high density collagen gels to drive hierarchical fiber formation for multiple musculoskeletal tissues. We found boundary conditions applied to high density collagen gels were capable of driving tenocytes, ligament fibroblasts, and meniscal fibrochondrocytes to develop native-sized hierarchical collagen fibers 20-40 μm in diameter. The fibers organize similar to bovine juvenile collagen with native fibril banding patterns and hierarchical fiber bundles 50-350 μm in diameter by 6 weeks. Mirroring fiber organization, tensile properties of restrained samples improved significantly with time, reaching ~1 MPa. Additionally, tendon, ligament, and meniscal cells produced significantly different sized fibers, different degrees of crimp, and different GAG concentrations, which corresponded with respective juvenile tissue. To our knowledge, these are some of the largest, most organized fibers produced to date in vitro. Further, cells produced tissue specific hierarchical fibers, suggesting this system is a promising tool to better understand cellular regulation of fiber formation to better stimulate it in vivo after injury.

摘要

分层胶原纤维是肌肉骨骼肌腱、韧带和半月板的主要强度来源。开发这些大纤维在工程替代物中或受伤后在体内仍然是一个挑战。本研究的目的是研究约束细胞接种高密度胶原凝胶在多种肌肉骨骼组织中驱动分层纤维形成的能力。我们发现,施加于高密度胶原凝胶的边界条件能够使肌腱细胞、韧带成纤维细胞和半月板纤维软骨细胞发育出直径为 20-40μm 的天然大小的分层胶原纤维。这些纤维的组织类似于具有天然原纤维带图案和直径为 50-350μm 的分层纤维束的牛幼年胶原。模仿纤维组织,受约束样品的拉伸性能随时间显著提高,达到约 1MPa。此外,肌腱、韧带和半月板细胞产生的纤维大小不同,卷曲程度不同,糖胺聚糖浓度也不同,这与相应的幼年组织相对应。据我们所知,这是迄今为止在体外产生的一些最大、最有组织的纤维。此外,细胞产生组织特异性的分层纤维,这表明该系统是一种有前途的工具,可以更好地理解细胞对纤维形成的调节,以便在受伤后更好地在体内刺激它。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7490/7883218/0c743cf056fd/fx1.jpg

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