Steck Eric, Bertram Helge, Abel Rainer, Chen Bohua, Winter Anja, Richter Wiltrud
Division of Experimental Orthopaedics, Orthopaedic Clinic, University of Heidelberg, Schlierbacher Landstr. 200a, D-69118 Heidelberg, Germany.
Stem Cells. 2005 Mar;23(3):403-11. doi: 10.1634/stemcells.2004-0107.
The potential of adult mesenchymal stem cells (MSCs) to differentiate towards cartilage, bone, adipose tissue, or muscle is well established. However, the capacity of MSCs to differentiate towards intervertebral disc (IVD)-like cells is unknown. The aim of this study was to compare the molecular phenotype of human IVD cells and articular chondrocytes and to analyze whether mesenchymal stem cells can differentiate towards both cell types after transforming growth factor beta (TGF beta)-mediated induction in vitro. Bone marrow-derived MSCs were differentiated in spheroid culture towards the chondrogenic lineage in the presence of TGF beta(3) dexamethasone, and ascorbate. A customized cDNA-array comprising 45 cartilage-, bone-, and stem cell-relevant genes was used to quantify gene expression profiles. After TGF beta-mediated differentiation, MSC spheroids turned positive for collagen type II protein and expressed a large panel of genes characteristic for chondrocytes, including aggrecan, decorin, fibromodulin, and cartilage oligomeric matrix protein, although at levels closer to IVD tissue than to hyaline articular cartilage. Like IVD tissue, the spheroids were strongly positive for collagen type I and osteopontin. MSC spheroids expressed more differentiation markers at higher levels than culture-expanded IVD cells and chondrocytes, which both dedifferentiated in monolayer culture. In conclusion, mesenchymal stem cells adopted a gene expression profile that resembled native IVD tissue more closely than native joint cartilage. Thus, these cells may represent an attractive source from which to obtain IVD-like cells, whereas modification of culture conditions is required to approach the molecular phenotype of chondrocytes in hyaline cartilage.
成人间充质干细胞(MSC)向软骨、骨、脂肪组织或肌肉分化的潜力已得到充分证实。然而,MSC向椎间盘(IVD)样细胞分化的能力尚不清楚。本研究的目的是比较人IVD细胞和关节软骨细胞的分子表型,并分析间充质干细胞在体外转化生长因子β(TGF-β)介导的诱导后是否能向这两种细胞类型分化。在存在TGF-β3、地塞米松和抗坏血酸的情况下,将骨髓来源的MSC在球体培养中向软骨形成谱系分化。使用包含45个与软骨、骨和干细胞相关基因的定制cDNA阵列来定量基因表达谱。在TGF-β介导的分化后,MSC球体II型胶原蛋白呈阳性,并表达了一大组软骨细胞特有的基因,包括聚集蛋白聚糖、核心蛋白聚糖、纤调蛋白和软骨寡聚基质蛋白,尽管其水平更接近IVD组织而非透明关节软骨。与IVD组织一样,球体I型胶原蛋白和骨桥蛋白呈强阳性。与在单层培养中均发生去分化的培养扩增的IVD细胞和软骨细胞相比,MSC球体在更高水平上表达更多的分化标志物。总之,间充质干细胞采用的基因表达谱比天然关节软骨更接近天然IVD组织。因此,这些细胞可能是获得IVD样细胞的有吸引力的来源,而需要改变培养条件以接近透明软骨中软骨细胞的分子表型。