Meniscus regeneration combining meniscus and mesenchymal stromal cells in a degradable meniscus implant: an in vitro study.

IF 3.2 3区 医学 Q3 CELL & TISSUE ENGINEERING European cells & materials Pub Date : 2019-08-12 DOI:10.22203/eCM.v038a05
Michella H. Hagmeijer, L. Vonk, M. Fenu, Y. W. V. Keep, A. Krych, Daniel B.F. Saris, Daniel B.F. Saris
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引用次数: 8

Abstract

Meniscus regeneration is an unmet clinical need as damage to the meniscus is common and causes early osteoarthritis. The aim of the present study was to investigate the feasibility of a one-stage cell-based treatment for meniscus regeneration by augmenting a resorbable collagen-based implant with a combination of recycled meniscus cells and mesenchymal stromal cells (MSCs). Cell communication and fate of the different cell types over time in co-culture were evaluated by connexin 43 staining for gap junctions and polymerase chain reaction (PCR) to discriminate between meniscus cells and MSCs, based on a Y-chromosome gene. To define optimal ratios, human meniscus cells and bone-marrow-derived MSCs were cultured in different ratios in cell pellets and type I collagen hydrogels. In addition, cells were seeded on the implant in fibrin glue by static seeding or injection. Cellular communication by gap junctions was shown in co-culture and a decrease in the amount of MSCs over time was demonstrated by PCR. 20 : 80 and 10 : 90 ratios showed significantly highest glycosaminoglycan and collagen content in collagen hydrogels. The same statistical trend was found in pellet cultures. Significantly more cells were present in the injected implant and cell distribution was more homogenous as compared to the statically seeded implant. The study demonstrated the feasibility of a new one-stage cell-based procedure for meniscus regeneration, using 20 % meniscus cells and 80 % MSCs seeded statically on the implant. In addition, the stimulatory effect of MSCs towards meniscus cells was demonstrated by communication through gap junctions.
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可降解半月板植入物中结合半月板和间充质基质细胞的半月板再生:一项体外研究。
半月板再生是一个未满足的临床需要,损伤半月板是常见的,并引起早期骨关节炎。本研究的目的是研究半月板再生的一期细胞治疗的可行性,通过增加可吸收的胶原基植入物,结合回收的半月板细胞和间充质间质细胞(MSCs)。基于y染色体基因,通过连接蛋白43对间隙连接染色和聚合酶链反应(PCR)来区分半月板细胞和间充质干细胞,评估不同细胞类型在共培养中随时间的细胞通讯和命运。为了确定最佳比例,我们将人半月板细胞和骨髓来源的间充质干细胞以不同比例培养在细胞颗粒和I型胶原水凝胶中。另外,用纤维蛋白胶静态播种或注射的方法将细胞播种到植入物上。在共培养中,细胞间通过间隙连接进行通信,PCR显示随着时间的推移,MSCs的数量减少。20:80和10:90比例的胶原水凝胶中糖胺聚糖和胶原含量最高。在颗粒培养中也发现了同样的统计趋势。与静态播种的种植体相比,注射的种植体中存在更多的细胞,细胞分布更加均匀。该研究证明了一种新的半月板细胞一期再生方法的可行性,将20%的半月板细胞和80%的间充质干细胞静态植入植入物。此外,MSCs对半月板细胞的刺激作用通过间隙连接被证实。
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来源期刊
European cells & materials
European cells & materials 生物-材料科学:生物材料
CiteScore
6.00
自引率
6.50%
发文量
55
审稿时长
1.5 months
期刊介绍: eCM provides an interdisciplinary forum for publication of preclinical research in the musculoskeletal field (Trauma, Maxillofacial (including dental), Spine and Orthopaedics). The clinical relevance of the work must be briefly mentioned within the abstract, and in more detail in the paper. Poor abstracts which do not concisely cover the paper contents will not be sent for review. Incremental steps in research will not be entertained by eCM journal.Cross-disciplinary papers that go across our scope areas are welcomed.
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