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在扩增阶段抑制 TGFβ 可增加人关节软骨细胞的软骨向再分化能力。

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

机构信息

Department of Orthopaedics, Erasmus MC, Rotterdam, The Netherlands.

出版信息

Osteoarthritis Cartilage. 2012 Oct;20(10):1152-60. doi: 10.1016/j.joca.2012.06.010. Epub 2012 Jul 4.

Abstract

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.

摘要

目的

自体软骨细胞移植是一种基于细胞的治疗方法,用于修复关节软骨缺损,依赖于可扩增(去分化)的软骨细胞。然而,扩增过程会导致几个表型变化,需要重新建立天然的软骨细胞表型以维持适当的修复。转化生长因子-β(TGFβ)等蛋白被认为会影响人关节软骨细胞(HAC)的软骨细胞再分化及其基质沉积。因此,我们研究了在扩增阶段去除 TGFβ 的影响。

设计

HAC 从关节软骨中分离出来,并在含有或不含有抗 TGFβ 抗体的常规血清补充培养基(胎牛血清(FCS))或化学定义(CD)培养基中进行扩增。通过球状体培养、基因表达分析和组织学评估细胞的再分化潜力。

结果

与 FCS 培养基相比,CD 培养基中的细胞增殖速度更快;抗 TGFβ 抗体的使用并不影响细胞增殖,但通过添加外源性 TGFβ1 进一步增加了细胞增殖,这是通过增加 p-Smad1/5/8 实现的。相反,在 FCS 培养基中,添加抗 TGFβ 抗体会降低细胞增殖和 p-Smad1/5/8 水平。在扩增过程中用抗 TGFβ 抗体挑战 FCS 或 CD 培养基都能增强随后的球状体培养中的软骨形成。此外,在 CD 培养基中扩增时去除 TGFβ 会抑制肥大标志物胶原 X 型(COL10)和基质金属蛋白酶 13(MMP-13)的 mRNA 表达。有趣的是,细胞扩增过程中酶联免疫吸附测定(ELISA)检测到的 TGFβ1 水平与再分化后 COL10 mRNA 表达相关。

结论

在扩增过程中去除 TGFβ 可提高软骨细胞的再分化能力并抑制肥大。这些结果表明,扩增培养基成分对改善软骨细胞的软骨形成再分化和抑制肥大具有重要意义。

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