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本文引用的文献

1
Update on hip and knee arthroplasty: current state of evidence.髋关节和膝关节置换术的最新进展:证据现状
Arthritis Rheum. 2005 Oct 15;53(5):772-80. doi: 10.1002/art.21465.
2
Roles of bHLH genes in neural stem cell differentiation.bHLH基因在神经干细胞分化中的作用。
Exp Cell Res. 2005 Jun 10;306(2):343-8. doi: 10.1016/j.yexcr.2005.03.015. Epub 2005 Apr 13.
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The role of type X collagen in facilitating and regulating endochondral ossification of articular cartilage.
Orthod Craniofac Res. 2005 Feb;8(1):11-7. doi: 10.1111/j.1601-6343.2004.00308.x.
4
Retroviral transduction with SOX9 enhances re-expression of the chondrocyte phenotype in passaged osteoarthritic human articular chondrocytes.用SOX9进行逆转录病毒转导可增强传代骨关节炎人关节软骨细胞中软骨细胞表型的重新表达。
Osteoarthritis Cartilage. 2005 Jan;13(1):80-9. doi: 10.1016/j.joca.2004.10.011.
5
Directing stem cell differentiation into the chondrogenic lineage in vitro.体外引导干细胞分化为软骨生成谱系。
Stem Cells. 2004;22(7):1152-67. doi: 10.1634/stemcells.2004-0062.
6
The combination of SOX5, SOX6, and SOX9 (the SOX trio) provides signals sufficient for induction of permanent cartilage.SOX5、SOX6和SOX9(SOX三联体)的组合提供了足以诱导永久性软骨形成的信号。
Arthritis Rheum. 2004 Nov;50(11):3561-73. doi: 10.1002/art.20611.
7
FGF-2 enhances the mitotic and chondrogenic potentials of human adult bone marrow-derived mesenchymal stem cells.成纤维细胞生长因子-2增强人成年骨髓间充质干细胞的有丝分裂和软骨形成潜能。
J Cell Physiol. 2005 May;203(2):398-409. doi: 10.1002/jcp.20238.
8
SOX9-dependent and -independent transcriptional regulation of human cartilage link protein.人软骨连接蛋白的SOX9依赖性和非依赖性转录调控
J Biol Chem. 2004 Dec 3;279(49):50942-8. doi: 10.1074/jbc.M406786200. Epub 2004 Sep 28.
9
Growth factor combination for chondrogenic induction from human mesenchymal stem cell.用于从人骨髓间充质干细胞诱导软骨生成的生长因子组合
Biochem Biophys Res Commun. 2004 Jul 30;320(3):914-9. doi: 10.1016/j.bbrc.2004.06.029.
10
Transduction of passaged human articular chondrocytes with adenoviral, retroviral, and lentiviral vectors and the effects of enhanced expression of SOX9.用腺病毒载体、逆转录病毒载体和慢病毒载体转导传代的人关节软骨细胞以及SOX9表达增强的影响。
Tissue Eng. 2004 Mar-Apr;10(3-4):575-84. doi: 10.1089/107632704323061933.

软骨形成中的软骨、SOX9和Notch信号

Cartilage, SOX9 and Notch signals in chondrogenesis.

作者信息

Hardingham Timothy E, Oldershaw Rachel A, Tew Simon R

机构信息

UK Centre for Tissue Engineering, Faculty of Life Sciences, University of Manchester, UK.

出版信息

J Anat. 2006 Oct;209(4):469-80. doi: 10.1111/j.1469-7580.2006.00630.x.

DOI:10.1111/j.1469-7580.2006.00630.x
PMID:17005019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2100356/
Abstract

Cartilage repair is an ongoing medical challenge. Tissue engineered solutions to this problem rely on the availability of appropriately differentiated cells in sufficient numbers. This review discusses the potential of primary human articular chondrocytes and mesenchymal stem cells to fulfil this role. Chondrocytes have been transduced with a retrovirus containing the transcription factor SOX9, which permits a greatly improved response of the cells to three-dimensional culture systems, growth factor stimulation and hypoxic culture conditions. Human mesenchymal stem cells have been differentiated into chondrocytes using well-established methods, and the Notch signalling pathway has been studied in detail to establish its role during this process. Both approaches offer insights into these in vitro systems that are invaluable to understanding and designing future cartilage regeneration strategies.

摘要

软骨修复是一项持续存在的医学挑战。针对这一问题的组织工程解决方案依赖于足够数量的适当分化细胞的可用性。本综述讨论了原代人关节软骨细胞和间充质干细胞发挥这一作用的潜力。软骨细胞已被含有转录因子SOX9的逆转录病毒转导,这使得细胞对三维培养系统、生长因子刺激和低氧培养条件的反应有了极大改善。人骨髓间充质干细胞已通过成熟方法分化为软骨细胞,并且对Notch信号通路进行了详细研究,以确定其在此过程中的作用。这两种方法都为这些体外系统提供了见解,这对于理解和设计未来的软骨再生策略非常宝贵。