Krassowska Anna, Gordon-Keylock Sabrina, Samuel Kay, Gilchrist Derek, Dzierzak Elaine, Oostendorp Robert, Forrester Lesley M, Ansell John D
John Hughes Bennett Laboratories, Division of Oncology, University of Edinburgh, Western General Hospital, Edinburgh, UK.
Exp Cell Res. 2006 Nov 1;312(18):3595-603. doi: 10.1016/j.yexcr.2006.08.001. Epub 2006 Aug 5.
We investigated whether the in vitro differentiation of ES cells into haematopoietic progenitors could be enhanced by exposure to the aorta-gonadal-mesonephros (AGM) microenvironment that is involved in the generation of haematopoietic stem cells (HSC) during embryonic development. We established a co-culture system that combines the requirements for primary organ culture and differentiating ES cells and showed that exposure of differentiating ES cells to the primary AGM region results in a significant increase in the number of ES-derived haematopoietic progenitors. Co-culture of ES cells on the AM20-1B4 stromal cell line derived from the AGM region also increases haematopoietic activity. We conclude that factors promoting the haematopoietic activity of differentiating ES cells present in primary AGM explants are partially retained in the AM20.1B4 stromal cell line and that these factors are likely to be different to those required for adult HSC maintenance.
我们研究了胚胎干细胞(ES细胞)在体外分化为造血祖细胞的过程是否能通过暴露于主动脉-性腺-中肾(AGM)微环境得到增强,该微环境在胚胎发育过程中参与造血干细胞(HSC)的产生。我们建立了一个将原代器官培养和分化ES细胞的要求相结合的共培养系统,并表明将分化的ES细胞暴露于原代AGM区域会导致ES来源的造血祖细胞数量显著增加。ES细胞与源自AGM区域的AM20-1B4基质细胞系共培养也会增加造血活性。我们得出结论,原代AGM外植体中促进分化ES细胞造血活性的因子部分保留在AM20.1B4基质细胞系中,并且这些因子可能与维持成体HSC所需的因子不同。