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地塞米松和三碘甲状腺原氨酸对原代牛软骨细胞及软骨分化间充质干细胞终末分化的影响

The effect of dexamethasone and triiodothyronine on terminal differentiation of primary bovine chondrocytes and chondrogenically differentiated mesenchymal stem cells.

作者信息

Randau Thomas M, Schildberg Frank A, Alini Mauro, Wimmer Matthias D, Haddouti El-Mustapha, Gravius Sascha, Ito Keita, Stoddart Martin J

机构信息

Department of Orthopedics and Trauma Surgery, University Clinic of Bonn, Bonn, Germany.

出版信息

PLoS One. 2013 Aug 16;8(8):e72973. doi: 10.1371/journal.pone.0072973. eCollection 2013.

Abstract

The newly evolved field of regenerative medicine is offering solutions in the treatment of bone or cartilage loss and deficiency. Mesenchymal stem cells, as well as articular chondrocytes, are potential cells for the generation of bone or cartilage. The natural mechanism of bone formation is that of endochondral ossification, regulated, among other factors, through the hormones dexamethasone and triiodothyronine. We investigated the effects of these hormones on articular chondrocytes and chondrogenically differentiated mesenchymal stem cells, hypothesizing that these hormones would induce terminal differentiation, with chondrocytes and differentiated stem cells being similar in their response. Using a 3D-alginate cell culture model, bovine chondrocytes and chondrogenically differentiated stem cells were cultured in presence of triiodothyronine or dexamethasone, and cell proliferation and extracellular matrix production were investigated. Collagen mRNA expression was measured by real-time PCR. Col X mRNA and alkaline phosphatase were monitored as markers of terminal differentiation, a prerequisite of endochondral ossification. The alginate culture system worked well, both for the culture of chondrocytes and for the chondrogenic differentiation of mesenchymal stem cells. Dexamethasone led to an increase in glycosaminoglycan production. Triiodothyronine increased the total collagen production only in chondrocytes, where it also induced signs of terminal differentiation, increasing both collagen X mRNA and alkaline phosphatase activity. Dexamethasone induced terminal differentiation in the differentiated stem cells. The immature articular chondrocytes used in this study seem to be able to undergo terminal differentiation, pointing to their possible role in the onset of degenerative osteoarthritis, as well as their potential for a cell source in bone tissue engineering. When chondrocyte-like cells, after their differentiation, can indeed be moved on towards terminal differentiation, they can be used to generate a model of endochondral ossification, but this limitation must be kept in mind when using them in cartilage tissue engineering application.

摘要

新兴的再生医学领域正在为治疗骨或软骨缺失及缺损提供解决方案。间充质干细胞以及关节软骨细胞是生成骨或软骨的潜在细胞。骨形成的自然机制是软骨内成骨,除其他因素外,该过程受激素地塞米松和三碘甲状腺原氨酸调控。我们研究了这些激素对关节软骨细胞和软骨分化的间充质干细胞的影响,推测这些激素会诱导终末分化,软骨细胞和分化的干细胞在反应上会相似。使用三维海藻酸盐细胞培养模型,将牛软骨细胞和软骨分化的干细胞在三碘甲状腺原氨酸或地塞米松存在的情况下进行培养,并研究细胞增殖和细胞外基质产生情况。通过实时PCR测量胶原蛋白mRNA表达。监测X型胶原蛋白mRNA和碱性磷酸酶作为终末分化的标志物,这是软骨内成骨的先决条件。海藻酸盐培养系统对软骨细胞培养和间充质干细胞的软骨分化均效果良好。地塞米松导致糖胺聚糖产量增加。三碘甲状腺原氨酸仅在软骨细胞中增加总胶原蛋白产量,在软骨细胞中它还诱导终末分化迹象,增加X型胶原蛋白mRNA和碱性磷酸酶活性。地塞米松在分化的干细胞中诱导终末分化。本研究中使用的未成熟关节软骨细胞似乎能够经历终末分化,这表明它们在退行性骨关节炎发病中的可能作用,以及它们作为骨组织工程细胞来源的潜力。当软骨样细胞分化后确实能够进一步走向终末分化时,它们可用于生成软骨内成骨模型,但在软骨组织工程应用中使用它们时必须牢记这一局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36f2/3745539/853160466f4e/pone.0072973.g001.jpg

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