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本文引用的文献

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Preparation of stem cell aggregates with gelatin microspheres to enhance biological functions.用明胶微球制备干细胞聚集体以增强生物学功能。
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Biomaterial-mediated delivery of microenvironmental cues for repair and regeneration of articular cartilage.生物材料介导的微环境线索传递在关节软骨修复和再生中的应用。
Mol Pharm. 2011 Aug 1;8(4):994-1001. doi: 10.1021/mp100437a. Epub 2011 Apr 22.
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Effect of a mechanical stimulation bioreactor on tissue engineered, scaffold-free cartilage.机械刺激生物反应器对组织工程无支架软骨的影响。
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Clinical and magnetic resonance imaging-based outcomes to 5 years after matrix-induced autologous chondrocyte implantation to address articular cartilage defects in the knee.基质诱导自体软骨细胞移植治疗膝关节关节软骨缺损 5 年后的临床和磁共振成像结果。
Am J Sports Med. 2011 Apr;39(4):753-63. doi: 10.1177/0363546510390476. Epub 2011 Jan 21.
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Gelatin microspheres crosslinked with genipin for local delivery of growth factors.基因胶微球用于生长因子局部递送的交联。
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Chondrogenic differentiation of human mesenchymal stem cells: a comparison between micromass and pellet culture systems.人骨髓间充质干细胞的软骨分化:微团和微载体球培养系统的比较。
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Membrane-based cultures generate scaffold-free neocartilage in vitro: influence of growth factors.基于膜的培养方法可在体外生成无支架的新生软骨:生长因子的影响。
Tissue Eng Part A. 2010 Feb;16(2):513-21. doi: 10.1089/ten.TEA.2009.0326.
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Production of hyaline-like cartilage by bone marrow mesenchymal stem cells in a self-assembly model.骨髓间充质干细胞在自组装模型中生成类透明软骨。
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Chondrogenic differentiation of human mesenchymal stem cell aggregates via controlled release of TGF-beta1 from incorporated polymer microspheres.通过掺入聚合物微球中 TGF-β1 的控制释放实现人骨髓间充质干细胞聚集体的软骨分化。
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In vitro generation of a scaffold-free tissue-engineered construct (TEC) derived from human synovial mesenchymal stem cells: biological and mechanical properties and further chondrogenic potential.源自人滑膜间充质干细胞的无支架组织工程构建体(TEC)的体外生成:生物学和力学特性以及进一步的软骨生成潜力。
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通过自组装的 hMSC 片与掺入的可生物降解的明胶微球释放转化生长因子-β1 来构建工程软骨。

Engineered cartilage via self-assembled hMSC sheets with incorporated biodegradable gelatin microspheres releasing transforming growth factor-β1.

机构信息

Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.

出版信息

J Control Release. 2012 Mar 10;158(2):224-32. doi: 10.1016/j.jconrel.2011.11.003. Epub 2011 Nov 10.

DOI:10.1016/j.jconrel.2011.11.003
PMID:22100386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3294133/
Abstract

Self-assembling cell sheets have shown great potential for use in cartilage tissue engineering applications, as they provide an advantageous environment for the chondrogenic induction of human mesenchymal stem cells (hMSCs). We have engineered a system of self-assembled, microsphere-incorporated hMSC sheets capable of forming cartilage in the presence of exogenous transforming growth factor β1 (TGF-β1) or with TGF-β1 released from incorporated microspheres. Gelatin microspheres with two different degrees of crosslinking were used to enable different cell-mediated microsphere degradation rates. Biochemical assays, histological and immunohistochemical analyses, and biomechanical testing were performed to determine biochemical composition, structure, and equilibrium modulus in unconfined compression after 3 weeks of culture. The inclusion of microspheres with or without loaded TGF-β1 significantly increased sheet thickness and compressive equilibrium modulus, and enabled more uniform matrix deposition by comparison to control sheets without microspheres. Sheets incorporated with fast-degrading microspheres containing TGF-β1 produced significantly more GAG and GAG per DNA than all other groups tested and stained more intensely for type II collagen. These findings demonstrate improved cartilage formation in microsphere-incorporated cell sheets, and describe a tailorable system for the chondrogenic induction of hMSCs without necessitating culture in growth factor-containing medium.

摘要

自组装细胞片层在软骨组织工程应用中显示出巨大的潜力,因为它们为人类间充质干细胞(hMSC)的软骨诱导提供了有利的环境。我们构建了一种自组装的、包含微球的 hMSC 片层系统,该系统能够在存在外源性转化生长因子 β1(TGF-β1)或包含微球释放的 TGF-β1 的情况下形成软骨。使用两种不同交联程度的明胶微球来实现不同的细胞介导的微球降解速率。进行了生化分析、组织学和免疫组织化学分析以及无约束压缩下的生物力学测试,以确定培养 3 周后的生化组成、结构和平衡模量。与不含微球的对照片层相比,包含负载 TGF-β1 的微球或不包含 TGF-β1 的微球的片层显著增加了片层厚度和压缩平衡模量,并能够更均匀地沉积基质。含有 TGF-β1 的快速降解微球的片层产生的 GAG 和 GAG 每 DNA 显著高于所有其他测试组,并且对 II 型胶原的染色更强烈。这些发现表明,微球掺入细胞片层中可改善软骨形成,并描述了一种可定制的 hMSC 软骨诱导系统,而无需在含生长因子的培养基中培养。