College of Medicine, Pochon CHA University, Seoul, Republic of Korea.
J Biomed Mater Res A. 2010 Mar 1;92(3):988-96. doi: 10.1002/jbm.a.32341.
In this study, in vivo studies, both nude mouse and rabbit cartilage defect, were tested for chondrogenesis using stem cells (SCs) using growth factor. Specifically, human mesenchymal stem cells (hMSCs) were embedded in a hydrogel scaffold, which was coencapsulated with transforming growth factor-beta3 (TGF-beta3). The specific extracellular matrices (ECMs) released from hMSCs transplanted into the animal were assessed via glycosaminoglycan (GAG)/DNA content, RT-PCR, real time-QPCR, immunohistochemical (IHC), and Safranin-O staining and were observed up to 7 weeks after injection. By detection of ECMs the GAG content per cell remained constant for all formulations, indicating that the dramatic increase in cell number for samples with TGF-beta3 was accompanied by the maintenance of the cell phenotypes. The histological and IHC staining of the newly repaired tissues observed after treatment with TGF-beta3 mixed with hMSCs evidenced hyaline cartilage-like characteristics. Moreover, the results observed with the animal model (rabbit) treated with hMSCs embedded in the growth factor-containing hydrogel indicate that the implantation of mixed cells with TGF-beta3 may constitute a clinically efficient method for the regeneration of hyaline articular cartilage.
在这项研究中,通过体内研究,使用生长因子对裸鼠和兔软骨缺损中的干细胞(SCs)进行软骨生成测试。具体来说,将人间充质干细胞(hMSCs)嵌入水凝胶支架中,该支架与转化生长因子-β3(TGF-β3)共包封。通过糖胺聚糖(GAG)/DNA 含量、RT-PCR、实时 QPCR、免疫组织化学(IHC)和番红 O 染色评估从移植到动物体内的 hMSCs 释放的特定细胞外基质(ECMs),并在注射后长达 7 周进行观察。通过检测 ECMs,所有配方的细胞内 GAG 含量保持不变,表明 TGF-β3 存在时细胞数量的大幅增加伴随着细胞表型的维持。用 TGF-β3 混合 hMSCs 处理后观察到的新修复组织的组织学和 IHC 染色显示出透明软骨样特征。此外,用含有生长因子的水凝胶包埋 hMSCs 处理的动物模型(兔)的结果表明,混合细胞与 TGF-β3 的植入可能构成透明关节软骨再生的有效临床方法。