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[与软骨细胞共培养的骨髓基质细胞在可生物降解支架上的软骨形成潜能:猪和小鼠的体内实验]

[Potential of chondrogenesis of bone marrow stromal cells co-cultured with chondrocytes on biodegradable scaffold: in vivo experiment with pigs and mice].

作者信息

Liu Xia, Zhou Guang-dong, Lü Xiao-jie, Liu Tian-yi, Zhang Wen-jie, Liu Wei, Cao Yi-lin

机构信息

Department of Plastic and Reconstructive Surgery, Shanghai 9th People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai Key Laboratory of Tissue Engineering, Shanghai 200011, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2007 Jul 17;87(27):1929-33.

Abstract

OBJECTIVE

To explore the feasibility of in vivo chondrogenesis of bone marrow stromal cells (BMSCs) co-cultured with chondrocytes on biodegradable scaffold.

METHODS

Porcine BMSCs were isolated, expanded and labeled with enhanced green fluorescent protein (EGFP), and then were mixed with articular chondrocytes isolated from porcine knee joint at the ratio of 1:1. The mixed cells were seeded onto polyglycolic acid (PGA) scaffold at the ultimate concentration of 5.0 x 10(7)/ml (co-culture group). Pure chondrocytes and BMSCs of the same ultimate concentration were seeded respectively onto the scaffold as positive control group and negative control group. After two weeks' culture in vitro, they were planted subcutaneously into nude mice respectively. These specimens were collected after in vivo implantation for 8 weeks to undergo microscopy. Laser confocal microscopy was used to observe the distribution of EGFP-labeled cells in the tissue. RT-PCR was used to examine the expression of collagen type II and aggrecan. Immunohistochemistry was used to observe the protein expression of collagen type II.

RESULTS

The cell-scaffold constructs of the co-culture group and positive control group, could maintain the original size and shape no matter in vitro or in vivo. After 8 weeks' in vivo implantation, the constructs in both co-culture group and positive control group formed cartilage-like tissue with typical histological structure and extracellular matrix staining similar to those of the normal cartilage. The GAG content and compressive modulus of the co-culture group reached over 80% of those of the positive control group. Confocal microscopy revealed the presence of EGFP-labeled cells in the engineered cartilage lacuna. Histological examination showed that the constructs of the negative control group shrunk gradually after in vivo implantation with no typical cartilage-like tissue formation.

CONCLUSION

In vitro co-cultured BMSC-chondrocyte-PGA constructs have the potential to form mature cartilage-like tissue in subcutaneous non-chondrogenesis environment, indicating that chondrocytes still provide enough signals for BMSC chondrogenic differentiation.

摘要

目的

探讨骨髓基质细胞(BMSCs)与软骨细胞在可生物降解支架上共培养进行体内软骨生成的可行性。

方法

分离、扩增猪BMSCs并用增强型绿色荧光蛋白(EGFP)标记,然后与从猪膝关节分离的关节软骨细胞按1:1比例混合。将混合细胞以最终浓度5.0×10(7)/ml接种到聚乙醇酸(PGA)支架上(共培养组)。将相同最终浓度的纯软骨细胞和BMSCs分别接种到支架上作为阳性对照组和阴性对照组。体外培养两周后,分别皮下植入裸鼠体内。体内植入8周后收集这些标本进行显微镜检查。采用激光共聚焦显微镜观察组织中EGFP标记细胞的分布。采用RT-PCR检测Ⅱ型胶原和聚集蛋白聚糖的表达。采用免疫组织化学观察Ⅱ型胶原的蛋白表达。

结果

共培养组和阳性对照组的细胞-支架构建体,无论在体外还是体内均能保持原始大小和形状。体内植入8周后,共培养组和阳性对照组的构建体均形成了具有典型组织结构和细胞外基质染色的软骨样组织,与正常软骨相似。共培养组的糖胺聚糖含量和压缩模量达到阳性对照组的80%以上。共聚焦显微镜显示工程化软骨陷窝中有EGFP标记的细胞。组织学检查显示,阴性对照组的构建体在体内植入后逐渐收缩,未形成典型的软骨样组织。

结论

体外共培养的BMSC-软骨细胞-PGA构建体有潜力在皮下非软骨生成环境中形成成熟的软骨样组织,表明软骨细胞仍为BMSC软骨分化提供足够的信号。

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