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Chondrogenic Differentiation Could Be Induced by Autologous Bone Marrow Mesenchymal Stem Cell-Derived Extracellular Matrix Scaffolds Without Exogenous Growth Factor

机译:没有外源性生长因子的自体骨髓间充质干细胞衍生的细胞外基质支架可诱导软骨分化

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We previously found that the combination of an autologous bone mesenchymal stem cell-derived extracellular matrix (aBMSC-dECM) scaffold with bone marrow stimulation could enhance hyaline cartilage regeneration. We suspected that chondrogenic differentiation could be induced by the aBMSC-dECM scaffold. This study aimed to investigate whether aBMSC-dECM scaffolds could promote chondrogenic differentiation without exogenous growth factors. BMSCs were seeded on aBMSC-dECM scaffolds and cultured in vitro with or without transforming growth factor-(3) (E+ or E- group). Atelocollagen scaffolds were used as controls (C+ or C- group). The chondrogenic differentiation was evaluated by histological, biochemical, and real-time polymerase chain reaction assays. After 3 weeks, cartilage-like tissue with a homogeneous structure, a high cartilaginous matrix content (proteoglycan and type II collagen), and high expression levels of cartilage-associated genes (COL2A1, ACAN, and SOX9) were observed in the E+, E-, and C+ groups. In addition, BMSCs in each scaffold (E group or C group) were preconditioned with chondrogenic media in vitro for 1 week, and then implanted in the backs of nude mice for 3 weeks. Three weeks later, cartilage matrix formation (proteoglycan and type II collagen) was achieved only in the E group, confirmed by safranin O staining and immunohistochemical staining for type II collagen. Taken together, these results indicate that aBMSC-dECM scaffolds could induce chondrogenic differentiation. Thus, they could be successful candidate scaffolds for cartilage tissue engineering.
机译:我们先前发现自体骨髓间充质干细胞衍生的细胞外基质(aBMSC-dECM)支架与骨髓刺激相结合可以增强透明软骨的再生。我们怀疑aBMSC-dECM支架可以诱导软骨分化。这项研究旨在调查aBMSC-dECM支架是否可以促进软骨分化,而无需外源性生长因子。将BMSCs接种在aBMSC-dECM支架上,并在有或没有转化生长因子-(3)(E +或E-组)的情况下进行体外培养。 Atelocollagen支架用作对照(C +或C-组)。通过组织学,生化和实时聚合酶链反应分析评估软骨分化。 3周后,在E +,E中观察到软骨样组织具有均匀的结构,高的软骨基质含量(蛋白聚糖和II型胶原)以及高表达的软骨相关基因(COL2A1,ACAN和SOX9)。 -和C +组。另外,将每个支架(E组或C组)中的BMSC在体外用软骨形成培养基预处理1周,然后在裸鼠的背部植入3周。三周后,仅在E组中实现了软骨基质的形成(蛋白聚糖和II型胶原蛋白),通过番红素O染色和II型胶原蛋白的免疫组织化学染色证实了这一点。综上所述,这些结果表明aBMSC-dECM支架可以诱导软骨分化。因此,它们可能是成功用于软骨组织工程的候选支架。

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