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牛骨髓间充质干细胞在微团培养体系中自发软骨分化过程中的基因表达谱

Gene expression profile of bovine bone marrow mesenchymal stem cell during spontaneous chondrogenic differentiation in pellet culture system.

作者信息

Bosnakovski Darko, Mizuno Morimichi, Kim Gonhyung, Takagi Satoshi, Okumur Masahiro, Fujinag Toru

机构信息

Laboratory of Veterinary Surgery, Department of Clinical Science, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.

出版信息

Jpn J Vet Res. 2006 Feb;53(3-4):127-39.

Abstract

Bovine bone marrow mesenchymal stem cells (MSCs) cultured in condensate culture, spontaneous and independent for any external biostimulants, undergo chondrogenic differentiation. In the present study, the bovine MSC chondrogenesis pathway was studied by analyzing stage-specific gene expression using quantitative "Real Time" reverse transcriptase polymerase chain reaction (qRT-PCR). Results showed that bovine MSCs underwent complete chondrogenesis; the initial stage was characterized by expression. of sox9 messenger ribonucleic acid (mRNA), followed by high transcription of chondrocyte specific genes, collagen type II and IX, biglycan and cartilage oligomeric matrix protein, and the final prehypertrophic and/or hypertrophic stage was distinguished by increased expression of collagen type X. From day 7 to day 14 of differentiation increased mRNA expression of the transforming growth factors beta1 and beta2, basic fibroblast growth factor (FGF 2), bone morphogenic protein 6 (BMP 6), insulin-like growth factors 1, parathyroid hormone related peptide and indian hedgehog (Ihh) were detected. These results suggest that these well know chondrogenic growth factors may play a role in bovine chondrogenesis in autocrine and/or paracrine manner. On day 21 of the culture, FGF 2, BMP 6 and Ihh were highly expressed, compared to cells cultured in monolayer manner, which suggests a possible function in maintaining the terminal stage of differentiation. This data extends our knowledge about the unusual species-specific bovine MSC chondrogenesis, allowing us to define the phenotype of the differentiated cells. Furthermore, this study contributes to our in understanding of known chondrogenic-growth factors in autocrine and/or paracrine manner playing a role in the spontaneous differentiation.

摘要

在无任何外部生物刺激剂的条件下,于凝聚培养中自发且独立培养的牛骨髓间充质干细胞(MSCs)会发生软骨形成分化。在本研究中,通过使用定量“实时”逆转录聚合酶链反应(qRT-PCR)分析阶段特异性基因表达,对牛MSCs的软骨形成途径进行了研究。结果表明,牛MSCs经历了完全的软骨形成过程;初始阶段的特征是sox9信使核糖核酸(mRNA)的表达,随后是软骨细胞特异性基因、II型和IX型胶原蛋白、双糖链蛋白聚糖和软骨寡聚基质蛋白的高转录,而最终的前肥大和/或肥大阶段的特征是X型胶原蛋白表达增加。在分化的第7天至第14天,检测到转化生长因子β1和β2、碱性成纤维细胞生长因子(FGF 2)、骨形态发生蛋白6(BMP 6)、胰岛素样生长因子1、甲状旁腺激素相关肽和印度刺猬因子(Ihh)的mRNA表达增加。这些结果表明,这些知名的软骨形成生长因子可能以自分泌和/或旁分泌方式在牛软骨形成中发挥作用。在培养的第21天,与单层培养的细胞相比,FGF 2、BMP 6和Ihh高度表达,这表明它们在维持分化的终末阶段可能具有功能。这些数据扩展了我们对牛MSCs不同寻常的物种特异性软骨形成的认识,使我们能够定义分化细胞的表型。此外,本研究有助于我们理解已知的软骨形成生长因子以自分泌和/或旁分泌方式在自发分化中发挥作用。

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