快速分离的软骨细胞和干细胞在三层胶原基支架上的共培养在山羊骨软骨缺损模型中的评价

Q3 Biochemistry, Genetics and Molecular Biology Biomaterials and biosystems Pub Date : 2022-12-01 DOI:10.1016/j.bbiosy.2022.100066
Tanya J. Levingstone , Eamon J. Sheehy , Conor J. Moran , Gráinne M. Cunniffe , Pedro J. Diaz Payno , Robert T. Brady , Henrique V. Almeida , Simon F. Carroll , John M. O’Byrne , Daniel J. Kelly , Pieter AJ. Brama , Fergal J. O’ Brien
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引用次数: 1

摘要

软骨具有较差的再生能力,因此关节表面的损伤是一个主要的临床挑战。最近的研究主要集中在组织工程和基于细胞的方法的发展,以治疗软骨和骨软骨损伤,目前临床可用的基于细胞的方法包括自体软骨细胞植入和基质辅助自体软骨细胞植入。然而,由于需要两阶段的外科手术和体外软骨细胞扩增阶段,这些方法有明显的缺点,这增加了后勤挑战、住院时间和成本。在这项研究中,我们假设播种具有再生潜力的仿生三层支架,与软骨细胞/髌下脂肪垫基质细胞共培养相比,可提高其再生能力。不需要长期体外培养的快速细胞分离技术被用于实现软骨细胞和基质细胞的共同培养,从而克服了现有基于细胞的技术的局限性。在大型山羊平动动物模型中,将无细胞和细胞种子支架植入股骨髁和滑车嵴内的骨软骨缺损中。虽然分析显示细胞植入支架组有延迟软骨下骨愈合的趋势,但在12个月的时间点上,无细胞组和细胞植入组产生的软骨和骨组织的质量和数量相当。该研究结果强化了仿生三层支架修复关节缺陷的潜力,但未能证明CC/FPMSC共培养对该支架有明显的益处。考虑到与细胞种子支架方法相关的额外成本和复杂性,本研究表明,使用无细胞三层支架治疗骨软骨缺损可能是一种更谨慎的临床方法。
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Evaluation of a co-culture of rapidly isolated chondrocytes and stem cells seeded on tri-layered collagen-based scaffolds in a caprine osteochondral defect model

Cartilage has poor regenerative capacity and thus damage to the joint surfaces presents a major clinical challenge. Recent research has focussed on the development of tissue-engineered and cell-based approaches for the treatment of cartilage and osteochondral injuries, with current clinically available cell-based approaches including autologous chondrocyte implantation and matrix-assisted autologous chondrocyte implantation. However, these approaches have significant disadvantages due to the requirement for a two-stage surgical procedure and an in vitro chondrocyte expansion phase which increases logistical challenges, hospital times and costs. In this study, we hypothesized that seeding biomimetic tri-layered scaffolds, with proven regenerative potential, with chondrocyte/infrapatellar fat pad stromal cell co-cultures would improve their regenerative capacity compared to scaffolds implanted cell-free. Rapid cell isolation techniques, without the requirement for long term in vitro culture, were utilised to achieve co-cultures of chondrocytes and stromal cells and thus overcome the limitations of existing cell-based techniques. Cell-free and cell-seeded scaffolds were implanted in osteochondral defects, created within the femoral condyle and trochlear ridge, in a translational large animal goat model. While analysis showed trends towards delayed subchondral bone healing in the cell-seeded scaffold group, by the 12 month timepoint the cell-free and cell-seeded groups yield cartilage and bone tissue with comparable quality and quantity. The results of the study reinforce the potential of the biomimetic tri-layered scaffold to repair joint defects but failed to demonstrate a clear benefit from the addition of the CC/FPMSC co-culture to this scaffold. Taking into consideration the additional cost and complexity associated with the cell-seeded scaffold approach, this study demonstrates that the treatment of osteochondral defects using cell-free tri-layered scaffolds may represent a more prudent clinical approach.

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