Goessler Urlich Reinhart, Bugert Peter, Bieback Karen, Deml Moritz, Sadick Haneen, Hormann Karl, Riedel Frank
Department of Otolaryngology, Head and Neck Surgery, Ruprecht-Karls-University Heidelberg, Faculty of Clinical Medicine Mannheim, Germany.
Cell Mol Biol Lett. 2005;10(2):345-62.
Traditional surgical methods for the reconstruction of cartilage defects rely on the transplantation of autologous and allogenous tissues. The disadvantages of these techniques are the limited availability of suitable tissues and the donor site morbidity of transplants. In addition, in cultured chondrocytes, the dedifferentiation of cells seems unavoidable during multiplication. In this study, we investigated the expression of distinct markers during the dedifferentiation of human chondrocytes (HC) and human mesenchymal stem cells (MSC) in cell culture using microarray technique, immunohistochemistry and RT-PCR. Transforming growth factor beta (TGFbeta) is a multifunctional peptide that plays play a crucial role in inducing and maintaining chondrogenic differentiation. In dedifferentiating chondrocytes, the gene for TGFbeta1 was constantly expressed, while the gene for TGFbeta2 was never expressed. The genes for TGFalpha, TGFbeta4 and TGFbetai were activated with ongoing dedifferentiation. TGFbeta-receptor 3 was constantly expressed, while the genes for the TGFbeta-receptors 1 and 2 were never expressed. Immunohistochemical staining for TGFbeta beta 3 revealed upregulation in the course of dedifferentiation. The genes for LTBP1 and LTBP2 were activated with ongoing dedifferentiation, whereas the gene for LTBP3 was constantly expressed, and negative results were obtained for the gene for LTBP4. The genes for LTBP1 and LTBP2 were activated with ongoing dedifferentiation. During chondrogenic differentiation, the MSCs constantly expressed TGFbeta1, beta2, beta3 and beta4. LTBP1, LTBP2 and TGFbeta-R3 were downregulated. In conclusion, TGFbeta3, TGFbeta4, TGFbetai, LTBP1 and LTBP2 may assist the process of dedifferentiation, while TGFbeta1 and beta2 might not be involved in this process. Of the TGFbeta-receptors, only type 3 might be involved in dedifferentiation.
传统的软骨缺损重建手术方法依赖于自体和异体组织移植。这些技术的缺点是合适组织的可用性有限以及移植供区的并发症。此外,在培养的软骨细胞中,细胞在增殖过程中似乎不可避免地会发生去分化。在本研究中,我们使用微阵列技术、免疫组织化学和逆转录聚合酶链反应,研究了细胞培养中人类软骨细胞(HC)和人间充质干细胞(MSC)去分化过程中不同标志物的表达。转化生长因子β(TGFβ)是一种多功能肽,在诱导和维持软骨形成分化中起关键作用。在去分化的软骨细胞中,TGFβ1基因持续表达,而TGFβ2基因从未表达。随着去分化的进行,TGFα、TGFβ4和TGFβi基因被激活。TGFβ受体3持续表达,而TGFβ受体1和2的基因从未表达。TGFβ3的免疫组织化学染色显示在去分化过程中上调。随着去分化的进行,LTBP1和LTBP2基因被激活,而LTBP3基因持续表达,LTBP4基因检测结果为阴性。随着去分化的进行,LTBP1和LTBP2基因被激活。在软骨形成分化过程中,间充质干细胞持续表达TGFβ1、β2、β3和β4。LTBP1、LTBP2和TGFβ-R3下调。总之,TGFβ3、TGFβ4、TGFβi、LTBP1和LTBP2可能有助于去分化过程,而TGFβ1和β2可能不参与此过程。在TGFβ受体中,只有3型可能参与去分化。