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首页> 外文期刊>Tissue engineering, Part C. Methods >Optimal Seeding Densities for In Vitro Chondrogenesis of Two- and Three-Dimensional- Isolated and -Expanded Bone Marrow-Derived Mesenchymal Stromal Stem Cells Within a Porous Collagen Scaffold
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Optimal Seeding Densities for In Vitro Chondrogenesis of Two- and Three-Dimensional- Isolated and -Expanded Bone Marrow-Derived Mesenchymal Stromal Stem Cells Within a Porous Collagen Scaffold

机译:多孔胶原支架内二维和三维分离和扩展的骨髓衍生间质基质干细胞的体外软骨形成的最佳播种密度。

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Bone marrow-derived mesenchymal stromal stem cells (BMSCs) are a promising cell source for treating articular cartilage defects. The objective of this study was to assess the impact of cell seeding density within a collagen I scaffold on in vitro BMSC chondrogenesis following isolation and expansion in two-dimensional (2D) and three-dimensional (3D) environments. It was hypothesized that both expansion protocols would produce BMSCs capable of hyaline-like chondrogenesis with an optimal seeding density of 10x10(6) cells/cm(3). Ovine BMSCs were isolated in a 2D environment by plastic adherence, expanded to passage two in flasks containing an expansion medium, and seeded within collagen I scaffolds at densities of 50, 10, 5, 1, and 0.5x10(6) BMSCs/cm(3). For 3D isolation and expansion, aspirates containing known quantities of mononucleated cells (bone marrow-derived mononucleated cells [BMNCs]) were seeded on scaffolds at 50, 10, 5, 1, and 0.5x10(6) BMNCs/cm(3) and cultured in the expansion medium for an equivalent duration to 2D expansion. Constructs were differentiated in vitro in the chondrogenic medium for 21 days and assessed with reverse-transcription quantitative polymerase chain reaction, safranin O staining, histological scoring using the Bern Score, collagen immunofluorescence, and glycosaminoglycan (GAG) quantification. Two-dimensional-expanded BMSCs seeded at all densities were capable of proteoglycan production and displayed increased expressions of aggrecan and collagen II messenger RNA (mRNA) relative to predifferentiation controls. Collagen II deposition was apparent in scaffolds seeded at 0.5-10x10(6) BMSCs/cm(3). Chondrogenesis of 2D-expanded BMSCs was most pronounced in scaffolds seeded at 5-10x10(6) BMSCs/cm(3) based on aggrecan and collagen II mRNA, safranin O staining, Bern Score, total GAG, and GAG/deoxyribonucleic acid (DNA). For 3D-expanded BMSC-seeded scaffolds, increased aggrecan and collagen II mRNA expressions relative to controls were noted with all densities. Proteoglycan deposition was present in scaffolds seeded at 0.5-50x10(6) BMNCs/cm(3), while collagen II deposition occurred in scaffolds seeded at 10-50x10(6) BMNCs/cm(3). The highest levels of aggrecan and collagen II mRNA, Bern Score, total GAG, and GAG/DNA occurred with seeding at 50x10(6) BMNCs/cm(3). Within a collagen I scaffold, 2D- and 3D-expanded BMSCs are capable of hyaline-like chondrogenesis with optimal cell seeding densities of 5-10x10(6) BMSCs/cm(3) and 50x10(6) BMNCs/cm(3), respectively.
机译:骨髓来源的间充质基质干细胞(BMSCs)是治疗关节软骨缺损的有前途的细胞来源。这项研究的目的是评估在二维(2D)和三维(3D)环境中分离和扩展后,胶原I支架中细胞播种密度对体外BMSC软骨形成的影响。假设这两个扩展协议将产生能够进行类似透明质酸软骨形成的BMSC,其最佳播种密度为10x10(6)细胞/ cm(3)。在2D环境中通过塑料粘附分离绵羊BMSC,在含有扩增培养基的烧瓶中扩增至第二代,然后以50、10、5、1和0.5x10(6)BMSCs / cm2的密度接种在I型胶原支架中。 3)。为了进行3D分离和扩展,将含有已知数量的单核细胞(骨髓来源的单核细胞[BMNCs])的吸出物以BMNCs / cm(3)和50、10、5、1和0.5x10(6)BMNCs和在扩展培养基中培养的时间与2D扩展相当。将构建体在软骨形成培养基中体外分化21天,并通过逆转录定量聚合酶链反应,番红蛋白O染色,使用伯恩评分的组织学评分,胶原蛋白免疫荧光和糖胺聚糖(GAG)定量进行评估。相对于预分化对照,以各种密度接种的二维扩增BMSCs都能够产生蛋白聚糖,并且显示出聚集蛋白聚糖和胶原蛋白II信使RNA(mRNA)的表达增加。胶原蛋白II沉积在以0.5-10x10(6)BMSCs / cm(3)接种的支架中很明显。基于聚集蛋白聚糖和胶原蛋白II mRNA,番红蛋白O染色,伯尔尼评分,总GAG和GAG /脱氧核糖核酸(DNA),以5-10x10(6)BMSCs / cm(3)接种的支架中,二维扩展BMSCs的软骨形成最明显。 )。对于3D扩增的BMSC种植支架,在所有密度下均观察到相对于对照,聚集蛋白聚糖和胶原II mRNA表达增加。蛋白聚糖沉积存在于以0.5-50x10(6)BMNCs / cm(3)接种的支架中,而胶原蛋白II沉积发生于以10-50x10(6)BMNCs / cm(3)接种的支架中。聚集蛋白聚糖和胶原蛋白II mRNA,Bern评分,总GAG和GAG / DNA的最高水平出现在播种为50x10(6)BMNCs / cm(3)的情况下。在胶原蛋白I支架内,2D和3D扩展的BMSC能够进行类似透明质酸的软骨生成,其最佳细胞接种密度为5-10x10(6)BMSCs / cm(3)和50x10(6)BMNCs / cm(3),分别。

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