Ikeda Toshiyuki, Kamekura Satoru, Mabuchi Akihiko, Kou Ikuyo, Seki Shoji, Takato Tsuyoshi, Nakamura Kozo, Kawaguchi Hiroshi, Ikegawa Shiro, Chung Ung-il
Laboratory for Bone & Joint Diseases, SNP Research Center, RIKEN (The Institute of Physical and Chemical Research), University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Arthritis Rheum. 2004 Nov;50(11):3561-73. doi: 10.1002/art.20611.
To regenerate permanent cartilage, it is crucial to know not only the necessary conditions for chondrogenesis, but also the sufficient conditions. The objective of this study was to determine the signal sufficient for chondrogenesis.
Embryonic stem cells that had been engineered to fluoresce upon chondrocyte differentiation were treated with combinations of factors necessary for chondrogenesis, and chondrocyte differentiation was detected as fluorescence. We screened for the combination that could induce fluorescence within 3 days. Then, primary mesenchymal stem cells, nonchondrogenic immortalized cell lines, and primary dermal fibroblasts were treated with the combination, and the induction of chondrocyte differentiation was assessed by detecting the expression of the cartilage marker genes and the accumulation of proteoglycan-rich matrix. The effects of monolayer, spheroid, and 3-dimensional culture systems on induction by combinations of transcription factors were compared. The effects of the combination on hypertrophic and osteoblastic differentiation were evaluated by detecting the expression of the characteristic marker genes.
No single factor induced fluorescence. Among various combinations examined, only the SOX5, SOX6, and SOX9 combination (the SOX trio) induced fluorescence within 3 days. The SOX trio successfully induced chondrocyte differentiation in all cell types tested, including nonchondrogenic types, and the induction occurred regardless of the culture system used. Contrary to the conventional chondrogenic techniques, the SOX trio suppressed hypertrophic and osteogenic differentiation at the same time.
These data strongly suggest that the SOX trio provides signals sufficient for the induction of permanent cartilage.
要再生永久性软骨,关键是不仅要了解软骨形成的必要条件,还要了解充分条件。本研究的目的是确定足以诱导软骨形成的信号。
经过基因工程改造、在软骨细胞分化时发出荧光的胚胎干细胞,用软骨形成所需的多种因子组合进行处理,通过检测荧光来检测软骨细胞分化情况。我们筛选出能在3天内诱导荧光的组合。然后,用该组合处理原代间充质干细胞、非软骨形成的永生化细胞系和原代真皮成纤维细胞,并通过检测软骨标记基因的表达和富含蛋白聚糖的基质的积累来评估软骨细胞分化的诱导情况。比较了单层、球体和三维培养系统对转录因子组合诱导作用的影响。通过检测特征性标记基因的表达来评估该组合对肥大和成骨分化的影响。
没有单一因子能诱导荧光。在所检测的各种组合中,只有SOX5、SOX6和SOX9组合(SOX三联体)能在3天内诱导荧光。SOX三联体成功地在所有测试细胞类型(包括非软骨形成类型)中诱导了软骨细胞分化,且诱导作用与所使用的培养系统无关。与传统的软骨形成技术相反,SOX三联体同时抑制了肥大和成骨分化。
这些数据有力地表明,SOX三联体提供了足以诱导永久性软骨的信号。