首页> 外文期刊>Osteoarthritis and cartilage >TGFβ inhibition during expansion phase increases the chondrogenic re-differentiation capacity of human articular chondrocytes
【24h】

TGFβ inhibition during expansion phase increases the chondrogenic re-differentiation capacity of human articular chondrocytes

机译:扩张期的TGFβ抑制作用增加了人关节软骨细胞的软骨形成再分化能力

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: Autologous chondrocyte implantation is a cell-based treatment to repair articular cartilage defects, relying on the availability of expanded (de-differentiated) chondrocytes. Unfortunately, the expansion process causes several phenotypical changes, requiring re-establishment of the native chondrogenic phenotype to sustain proper repair. Among other proteins, transforming growth factor-β (TGFβ) is known to influence the chondrogenic re-differentiation of human articular chondrocytes (HACs) and their matrix deposition. Thus we investigated the effects of TGFβ-depletion during the expansion phase. Design: HACs were isolated from articular cartilage and expanded in the canonical serum-supplemented medium [fetal calf serum (FCS)] or in a chemically-defined (CD) medium, with or without anti-TGFβ antibody administration. The re-differentiation potential of the cells was assessed by pellet cultures, gene expression analysis and histology. Results: Cell proliferation proceeded more rapidly in CD-medium than in FCS-medium; it was not affected by the use of anti-TGFβ antibody but was further increased by addition of exogenous TGFβ1, via increased p-Smad1/5/8. Conversely, in FCS-medium, addition of anti-TGFβ antibody decreased both proliferation and p-Smad1/5/8 level. Challenging either FCS- or CD-medium with anti-TGFβ antibody during expansion enhanced chondrogenesis in the subsequent pellet cultures. Moreover, TGFβ-depletion during expansion in CD-medium inhibited mRNA expression of hypertrophic markers, collagen type-X (COL10) and matrix metalloproteinase-13 (MMP-13). Interestingly, the TGFβ1 level detected by enzyme-linked immunosorbent sandwich assay (ELISA) during cell expansion was correlated with COL10 mRNA expression after re-differentiation. Conclusion: TGFβ-depletion during expansion improves the re-differentiation capacity of chondrocytes and inhibits hypertrophy. These results indicate the importance of the expansion medium composition to improve chondrogenic re-differentiation and to inhibit hypertrophy.
机译:目的:自体软骨细胞植入是一种基于细胞的修复关节软骨缺损的治疗方法,依赖于可扩展(去分化)软骨细胞的可用性。不幸的是,扩增过程会引起一些表型改变,需要重建天然软骨形成表型以维持适当的修复。在其他蛋白质中,已知转化生长因子-β(TGFβ)影响人关节软骨细胞(HAC)的软骨生成再分化及其基质沉积。因此,我们研究了扩张期TGFβ耗竭的影响。设计:从关节软骨中分离HAC,并在添加或不添加抗TGFβ抗体的情况下,在标准血清补充培养基[胎牛血清(FCS)]或化学成分明确的(CD)培养基中扩增。通过沉淀培养,基因表达分析和组织学评估细胞的再分化潜能。结果:CD培养基中细胞的增殖比FCS培养基中的细胞增殖更快。它不受使用抗TGFβ抗体的影响,但通过增加p-Smad1 / 5/8通过添加外源TGFβ1进一步增加。相反,在FCS培养基中,添加抗TGFβ抗体会降低增殖和p-Smad1 / 5/8水平。在扩增过程中用抗TGFβ抗体挑战FCS或CD培养基可增强随后的沉淀培养物中的软骨形成。此外,在CD培养基中扩增过程中TGFβ耗竭抑制了肥大标记,X型胶原(COL10)和基质金属蛋白酶13(MMP-13)的mRNA表达。有趣的是,在细胞分化过程中通过酶联免疫吸附三明治测定法(ELISA)检测到的TGFβ1水平与再分化后的COL10 mRNA表达相关。结论:扩张过程中TGFβ的缺失可提高软骨细胞的再分化能力并抑制肥大。这些结果表明,膨胀培养基组合物对于改善软骨原性再分化和抑制肥大的重要性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号