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首页> 外文期刊>Journal of tissue engineering and regenerative medicine >Engineering cartilaginous grafts using chondrocyte-laden hydrogels supported by a superficial layer of stem cells
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Engineering cartilaginous grafts using chondrocyte-laden hydrogels supported by a superficial layer of stem cells

机译:使用由干细胞表面浅表的软骨细胞 - 升起水凝胶的工程软骨移植物

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摘要

During postnatal joint development, progenitor cells that reside in the superficial region of articular cartilage first drive the rapid growth of the tissue and later help direct the formation of mature hyaline cartilage. These developmental processes may provide directions for the optimal structuring of co-cultured chondrocytes (CCs) and multipotent stromal/stem cells (MSCs) required for engineering cartilaginous tissues. The objective of this study was to engineer cartilage grafts by recapitulating aspects of joint development where a population of superficial progenitor cells drives the development of the tissue. To this end, MSCs were either self-assembled on top of CC-laden agarose gels (structured co-culture) or were mixed with CCs before being embedded in an agarose hydrogel (mixed co-culture). Porcine infrapatellar fat pad-derived stem cells (FPSCs) and bone marrowderived MSCs (BMSCs) were used as sources of progenitor cells. The DNA, sGAG and collagen content of a mixed co-culture of FPSCs and CCs was found to be lower than the combined content of two control hydrogels seeded with CCs and FPSCs only. In contrast, a mixed co-culture of BMSCs and CCs led to increased proliferation and sGAG and collagen accumulation. Of note was the finding that a structured co-culture, at the appropriate cell density, led to greater sGAG accumulation than a mixed co-culture for both MSC sources. In conclusion, assembling MSCs onto CC-laden hydrogels dramatically enhances the development of the engineered tissue, with the superficial layer of progenitor cells driving CC proliferation and cartilage ECM production, mimicking certain aspects of developing cartilage. Copyright (C) 2015 John Wiley & Sons, Ltd.
机译:在产后关节开发期间,位于关节软骨浅地区的祖细胞首先驱动组织的快速生长,并帮助直接形成成熟透明软骨的形成。这些发展过程可以提供工程软骨组织所需的共培养的软骨细胞(CCS)和多能基基/干细胞(MSCs)的最佳结构的方向。本研究的目的是通过重新构建联合发展的方面来工程包围地移植物,其中浅表祖细胞群驱动组织的发展。为此,MSCs在CC-Laden琼脂糖凝胶(结构化共培养)顶部上是自组装的,或者在嵌入琼脂糖水凝胶(混合共培养)之前与CC混合。猪腋kATELLAR脂肪垫衍生的干细胞(FPSC)和骨髓状MSCs(BMSCs)用作祖细胞的来源。发现FPSCS和CCS的混合共培养的DNA,SGAG和胶原含量低于用CCS和FPSC种植的两种对照水凝胶的组合含量。相反,BMSCs和CCS的混合共培养导致增殖和SGAG和胶原蛋白积累。注意事项是,在适当的细胞密度下,在适当的细胞密度下导致了比MSC源的混合共同培养更大的SGAG积累。总之,将MSC组装到CC-Laden水凝胶上显着增强了工程化组织的发育,吞噬细胞的浅层细胞,驱动CC增殖和软骨ECM生产,模仿了开发软骨的某些方面。版权所有(c)2015 John Wiley&Sons,Ltd。

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