首页> 外文期刊>Biomacromolecules >Co-delivery of Adipose-Derived Stem Cells and Growth Factor-Loaded Microspheres in RGD-Grafted N-Methacrylate Glycol Chitosan Gels for Focal Chondral Repair
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Co-delivery of Adipose-Derived Stem Cells and Growth Factor-Loaded Microspheres in RGD-Grafted N-Methacrylate Glycol Chitosan Gels for Focal Chondral Repair

机译:RGD接枝的N-甲基丙烯酸乙二醇酯壳聚糖凝胶中的脂肪干细胞和负载有生长因子的微球的共递送,用于软骨的局部修复。

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The coencapsulation of growth factor-loaded microspheres with adipose-derived stem cells (ASCs) within a hydrogel matrix was studied as a potential means to enhance ASC chondrogenesis in the development of a cell-based therapeutic strategy for the regeneration of partial thickness chondral defects. A photopolymerizable N-methacrylate glycol chitosan (MGC) was employed to form an in situ gel used to encapsulate microspheres loaded with bone morphogenetic protein 6 (BMP-6) and transforming growth factor-β3 (TGF-β3) with human ASCs. ASC viability and retention were enhanced when the Young's modulus of the MGC ranged between 225 and 380 kPa. Grafting an RGD-containing peptide onto the MGC backbone (RGD-MGC) improved ASC viability within the gels, remaining at greater than 90% over 14 days in culture. The effects of BMP-6 and TGF-β3 released from the polymer microspheres on ASC chondrogenesis were assessed, and the level of differentiation was compared to ASCs in control gels containing nongrowth factor-loaded microspheres cultured with and without the growth factors supplied in the medium. There was enhanced expression of chondrogenic markers at earlier time points when the ASCs were induced with the sustained and local release of BMP-6 and TGF-β3 from the microspheres. More specifically, the normalized glycosaminoglycan and collagen type II protein expression levels were significantly higher than in the controls. In addition, the ratio of collagen type II to type I was significantly higher in the microsphere delivery group and increased over time. End-point RT-PCR analysis supported that there was a more rapid induction and enhancement of ASC chondrogenesis in the controlled release group. Interestingly, in all of the assays, there was evidence of chondrogenic differentiation when the ASCs were cultured in the gels in the absence of growth factor stimulation. Overall, the co-delivery of growth-factor-loaded microspheres and ASCs in RGD-modified MGC gels successfully induced ASC chondrogenesis and is a promising strategy for cartilage repair.
机译:研究了将生长因子负载的微球与脂肪来源的干细胞(ASC)在水凝胶基质中的共包封,这是在开发基于细胞的部分厚度软骨缺损再生治疗方法中增强ASC软骨形成的潜在手段。使用可光聚合的N-甲基丙烯酸乙二醇酯壳聚糖(MGC)形成原位凝胶,该凝胶用于封装载有骨形态发生蛋白6(BMP-6)和人类ASC转化生长因子-β3(TGF-β3)的微球。当MGC的杨氏模量在225至380 kPa之间时,ASC的生存力和保留能力得到增强。将包含RGD的肽接枝到MGC主链(RGD-MGC)上可改善凝胶内的ASC生存力,在培养14天后仍保持90%以上。评估了从聚合物微球中释放的BMP-6和TGF-β3对ASC软骨形成的影响,并将其分化水平与含有凝胶的对照凝胶中的ASC进行了比较,该凝胶含有无生长因子的微球,培养基中有或没有培养基。当BSC-6和TGF-β3从微球体持续和局部释放诱导ASC时,软骨形成标记的表达在更早的时间增强。更具体地,归一化的糖胺聚糖和II型胶原蛋白表达水平显着高于对照。另外,在微球递送组中II型胶原蛋白与I型胶原蛋白的比例显着更高,并且随时间增加。终点RT-PCR分析支持在控释组中更快地诱导和增强ASC软骨形成。有趣的是,在所有测定中,当在没有生长因子刺激的情况下在凝胶中培养ASC时,都有软骨分化的证据。总体而言,在RGD修饰的MGC凝胶中共同装载生长因子的微球和ASC成功诱导了ASC软骨形成,并且是软骨修复的有前途的策略。

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