MRC Centre for Regenerative Medicine, John Hughes Bennett Laboratory, Queens Medical Research Institute, Edinburgh, United Kingdom.
Stem Cells Dev. 2010 Nov;19(11):1687-98. doi: 10.1089/scd.2009.0467. Epub 2010 Sep 9.
Hematopoietic differentiation of embryonic stem (ES) cells can be enhanced by co-culture with stromal cells derived from hematopoietic tissues and by overexpression of the transcription factor HOXB4. In this study, we compare the hematopoietic inductive effects of stromal cell lines derived from different subregions of the embryonic aorta-gonad-mesonephros tissue with the commonly used OP9 stromal cell line and with HOXB4 activation. We show that stromal cell lines derived from the aorta and surrounding mesenchyme (AM) act at an earlier stage of the differentiation process compared with the commonly used OP9 stromal cells. AM stromal cells were able to promote the further differentiation of isolated brachyury-GFP(+) mesodermal cells into hematopoietic progenitors, whereas the OP9 stromal cells could not support the differentiation of these cells. Co-culture and analyses of individual embryoid bodies support the hypothesis that the AM stromal cell lines could enhance the de novo production of hematopoietic progenitors, lending support to the idea that AM stromal cells might act on prehematopoietic mesoderm. The induction level observed for AM stromal cells was comparable to HOXB4 activation, but no additive effect was observed when these 2 inductive strategies were combined. Addition of a γ-secretase inhibitor reduced the inductive effects of both the stromal cell line and HOXB4, providing clues to possible shared molecular mechanisms.
胚胎干细胞(ES)的造血分化可以通过与造血组织来源的基质细胞共培养和过表达转录因子 HOXB4 来增强。在这项研究中,我们比较了源自胚胎主动脉-性腺-中肾组织不同亚区的基质细胞系与常用的 OP9 基质细胞系以及 HOXB4 激活的造血诱导作用。我们表明,与常用的 OP9 基质细胞相比,源自主动脉和周围间质(AM)的基质细胞系在分化过程的早期阶段起作用。AM 基质细胞能够促进分离的 brachyury-GFP(+)中胚层细胞进一步分化为造血祖细胞,而 OP9 基质细胞不能支持这些细胞的分化。共培养和单个胚状体的分析支持 AM 基质细胞系可以增强造血祖细胞的从头产生的假说,支持 AM 基质细胞可能作用于造血前中胚层的观点。观察到的 AM 基质细胞的诱导水平与 HOXB4 激活相当,但当这 2 种诱导策略结合使用时,没有观察到相加效应。添加 γ-分泌酶抑制剂可降低基质细胞系和 HOXB4 的诱导作用,为可能存在的共同分子机制提供了线索。