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用5-氟尿嘧啶消融增殖的骨髓可实现间充质干细胞的部分纯化。

Ablation of proliferating marrow with 5-fluorouracil allows partial purification of mesenchymal stem cells.

作者信息

Wang Zhuo, Song Junhui, Taichman Russell S, Krebsbach Paul H

机构信息

Department of Biologic and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, 48109, USA.

出版信息

Stem Cells. 2006 Jun;24(6):1573-82. doi: 10.1634/stemcells.2005-0399.

Abstract

The ability to identify and maintain mesenchymal stem cells in vitro is a prerequisite for the ex vivo expansion of cells capable of effecting mesenchymal tissue regeneration. The aim of this investigation was to develop an assay to enrich and ultimately purify mesenchymal stem cells. To enrich the population of mesenchymal stem cell-like cells, rats or mice were administered 5-fluorouracil (5-FU) in vivo. Limiting dilution analysis demonstrated that 5-FU-treated bone marrow had the potential to form colony-forming units-fibroblastic (CFU-F) at a 10-fold or sixfold enrichment compared to normal bone marrow in rats or mice, respectively. In vivo and in vitro differentiation assays supported the enrichment and purification effects. In vitro, bone marrow cultures from 5-FU-treated bone marrow demonstrated lineage-specific gene expression in lineage-specific medium conditions in contrast to the multilineage gene expression of control bone marrow cultures. In vivo implantation of 5-FU-treated cells that were not expanded in culture generated ossicles containing an intact bone cortex and mature hematopoietic components, whereas non-5-FU-treated bone marrow only formed fibrous tissues. Our results demonstrate that enrichment of a quiescent cell population in the bone marrow by in vivo treatment of 5-FU spares those undifferentiated mesenchymal stem cells and influences the differentiation of bone marrow stromal cells in vitro and in vivo. This prospective identification of a population of mesenchymal cells from the marrow that maintain their multilineage potential should lead to more focused studies on the characterization of a true mesenchymal stem cell.

摘要

在体外鉴定和维持间充质干细胞的能力是能够实现间充质组织再生的细胞进行体外扩增的前提条件。本研究的目的是开发一种用于富集并最终纯化间充质干细胞的检测方法。为了富集间充质干细胞样细胞群体,对大鼠或小鼠进行体内5-氟尿嘧啶(5-FU)给药。有限稀释分析表明,与正常大鼠或小鼠骨髓相比,经5-FU处理的骨髓分别具有以10倍或6倍富集形成成纤维细胞集落形成单位(CFU-F)的潜力。体内和体外分化检测支持了富集和纯化效果。在体外,与对照骨髓培养物的多谱系基因表达相反,来自经5-FU处理的骨髓的骨髓培养物在谱系特异性培养基条件下表现出谱系特异性基因表达。将未经体外扩增的经5-FU处理的细胞进行体内植入可生成含有完整骨皮质和成熟造血成分的小骨,而未经5-FU处理的骨髓仅形成纤维组织。我们的结果表明,通过体内5-FU处理富集骨髓中的静止细胞群体可使那些未分化的间充质干细胞得以保留,并影响骨髓基质细胞在体外和体内的分化。这种从骨髓中前瞻性鉴定出具有多谱系潜能的间充质细胞群体的方法,应会促使对真正间充质干细胞特性的研究更加聚焦。

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