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从鼠骨髓中生成间充质干细胞系。

Generation of mesenchymal stem cell lines from murine bone marrow.

机构信息

Stem Cell & Molecular Biology Laboratory (201), Bhupat and Jyoti Mehta School of Biosciences, Department of Biotechnology, Indian Institute of Technology Madras, Chennai 600 036 TN, India.

出版信息

Cell Tissue Res. 2012 Oct;350(1):55-68. doi: 10.1007/s00441-012-1458-9. Epub 2012 Jul 27.

Abstract

Mesenchymal stem cells (MSC), because of their multipotency and ease of purification and amplification, are an ideal stem cell source for cell therapies. Bone-marrow-derived stem cells (BMSC) can be used to develop MSC-like immortalized cell lines with large proliferation and differentiation potentialities. Their immortalized status prevents the maintenance of MSC function and characters; this can be negated by modifying the isolation and maintenance protocol. Adult murine BMSC were isolated and maintained in media without additional growth factors together with passage-dependent reseeding following trypsinization. Cells maintained over 25 passages were considered as putative cell lines and characterized. The phenotypic and genotypic characteristics and multilineage differentiation potential of the cells were assessed by morphological, phenotypic, and molecular assays at various passages. The putative BMSC cell lines showed the characteristics of MSC and were able to maintain these characteristics, even after immortalization. The phenotypic data demonstrated difference among two cell lines; this was further validated by the difference in their multilineage differentiation potential following specific induction. More importantly, no changes were observed in the genotypic level in comparison with control cells, even after more than 50 passages. Our protocol thus advances the isolation and maintenance of BMSC and the development of putative BMSC cell lines that maintain characteristics of MSC, including multilineage differentiation potential, after more than 40 passages.

摘要

间充质干细胞(MSC)由于其多能性以及易于纯化和扩增,是细胞治疗的理想干细胞来源。骨髓来源的干细胞(BMSC)可用于开发具有大增殖和分化潜能的 MSC 样永生化细胞系。它们的永生化状态阻止了 MSC 功能和特征的维持;通过修改分离和维持方案可以否定这一点。分离和维持成年鼠 BMSC 时,在没有额外生长因子的培养基中进行,并在胰蛋白酶消化后进行传代依赖性再接种。被认为是假定细胞系的细胞在超过 25 代的培养中进行了特征鉴定。通过在不同代次进行形态学、表型和分子检测,评估了细胞的表型和基因型特征以及多能分化潜能。假定的 BMSC 细胞系表现出 MSC 的特征,并且即使在永生化后也能够维持这些特征。表型数据表明两个细胞系之间存在差异;通过特定诱导后的多能分化潜能差异进一步验证了这一点。更重要的是,与对照细胞相比,即使在超过 50 代之后,在基因型水平上也没有观察到变化。因此,我们的方案推进了 BMSC 的分离和维持,以及假定 BMSC 细胞系的开发,这些细胞系在超过 40 代的培养后仍能保持 MSC 的特征,包括多能分化潜能。

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