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将啮齿动物骨髓间充质干细胞与大鼠椎间盘组织共培养后向椎间盘样细胞的分化

Differentiation of rodent bone marrow mesenchymal stem cells into intervertebral disc-like cells following coculture with rat disc tissue.

作者信息

Wei Aiqun, Chung Sylvia A, Tao Helen, Brisby Helena, Lin Zhen, Shen Bojiang, Ma David D F, Diwan Ashish D

机构信息

Department of Orthopaedic Surgery, Orthopaedic Research Institute, St George Hospital, University of New South Wales, Sydney, NSW, Australia.

出版信息

Tissue Eng Part A. 2009 Sep;15(9):2581-95. doi: 10.1089/ten.TEA.2008.0458.

Abstract

This study aimed to evaluate whether rat mesenchymal stem cells (rMSCs) could be differentiated in vitro into disc-like cells by coculturing with intervertebral disc tissue. rMSCs were cultured with rodent intervertebral disc for up to 30 days in transwell plates. The differentiation of rMSCs was evaluated by immunostaining, Western blot, real-time RT-PCR, Northern blot, and electron microscopy. The potentials of multilineage differentiation and proteoglycan and collagen synthesis were also investigated. rMSCs underwent morphological changes to form three-dimensional micromasses and expressed collagen-2, aggrecan, and sox-9 at RNA and protein levels after 14 days of coculture. These changes were not detected in the samples of rMSCs cultured alone. Cocultured rMSCs also showed other characteristic features of disc-like cells, including the extracellular matrix formation, and proteoglycan and collagen synthesis. In addition, cellular contact between cocultured rMSCs and disc tissue was observed by electron microscopy. Committed rMSCs still retained their differentiation ability into mesoderm lineages of adipocytes or osteocytes when the local environment was altered. This study supports that MSCs are a promising source for cell therapy and tissue engineering in disc regeneration, and highlights that rMSCs can be induced into nucleus pulposus-like cells in vitro under the direct influence of intact disc tissue.

摘要

本研究旨在评估大鼠间充质干细胞(rMSCs)与椎间盘组织共培养时能否在体外分化为盘状细胞。rMSCs在transwell板中与啮齿动物椎间盘共培养长达30天。通过免疫染色、蛋白质印迹、实时逆转录聚合酶链反应、Northern印迹和电子显微镜评估rMSCs的分化情况。还研究了多谱系分化以及蛋白聚糖和胶原蛋白合成的潜力。共培养14天后,rMSCs发生形态变化形成三维微团,并在RNA和蛋白质水平表达胶原蛋白-2、聚集蛋白聚糖和sox-9。在单独培养的rMSCs样本中未检测到这些变化。共培养的rMSCs还表现出盘状细胞的其他特征,包括细胞外基质形成以及蛋白聚糖和胶原蛋白合成。此外,通过电子显微镜观察到共培养的rMSCs与椎间盘组织之间的细胞接触。当局部环境改变时,定向的rMSCs仍保留其向脂肪细胞或骨细胞等中胚层谱系分化的能力。本研究支持间充质干细胞是椎间盘再生细胞治疗和组织工程的有前景的细胞来源,并强调在完整椎间盘组织的直接影响下,rMSCs可在体外诱导分化为髓核样细胞。

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