Suppr超能文献

成纤维细胞生长因子可诱导胎儿前脑祖细胞以及胚胎干细胞分化过程中的神经干细胞表型。

Fibroblast growth factor induces a neural stem cell phenotype in foetal forebrain progenitors and during embryonic stem cell differentiation.

作者信息

Pollard Steven M, Wallbank Richard, Tomlinson Simon, Grotewold Lars, Smith Austin

机构信息

Wellcome Trust Centre for Stem Cell Research, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QR, UK.

出版信息

Mol Cell Neurosci. 2008 Jul;38(3):393-403. doi: 10.1016/j.mcn.2008.03.012. Epub 2008 Apr 10.

Abstract

Neural stem (NS) cell lines may be derived via differentiation of pluripotent embryonic stem (ES) cells or from foetal forebrain. However, because NS cells arise in vitro from heterogeneous populations their immediate cellular origin remains unclear. We used microarray-based expression profiling to identify a set of markers expressed by mouse NS cells but not ES cells. One differentially expressed gene encodes the cell surface protein, CD44. CD44 expression is activated by FGF-2 in a subset of cells in both differentiating ES cells and foetal forebrain cultures. Following isolation by flow cytometry the CD44+ population was found to be highly enriched for NS cell founders. We found that other NS cell marker genes are also induced by FGF in culture, including: Adam12, Cadherin20, Cx3cl1, EGFR, Frizzled9, Kitl, Olig1, Olig2 and Vav3. We speculate that the self-renewing NS cell state may be generated in vitro following transcriptional resetting induced by FGF.

摘要

神经干细胞(NS)系可通过多能胚胎干细胞(ES)的分化或从胎儿前脑获得。然而,由于NS细胞在体外源自异质群体,其直接的细胞起源仍不清楚。我们使用基于微阵列的表达谱分析来鉴定一组由小鼠NS细胞而非ES细胞表达的标志物。一个差异表达基因编码细胞表面蛋白CD44。在分化的ES细胞和胎儿前脑培养物的一部分细胞中,FGF-2可激活CD44的表达。通过流式细胞术分离后,发现CD44+群体高度富集NS细胞祖细胞。我们发现,培养中其他NS细胞标志物基因也由FGF诱导,包括:Adam12、钙黏蛋白20、Cx3cl1、表皮生长因子受体(EGFR)、卷曲蛋白9、Kitl、少突胶质细胞转录因子1(Olig1)、少突胶质细胞转录因子2(Olig2)和Vav3。我们推测,在FGF诱导的转录重设后,体外可能产生自我更新的NS细胞状态。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验