Taoudi Samir, Gonneau Christèle, Moore Kate, Sheridan Julie M, Blackburn C Clare, Taylor Erin, Medvinsky Alexander
MRC Centre for Regenerative Medicine, Institute for Stem Cell Research, University of Edinburgh, Edinburgh EH9 3JQ, UK.
Cell Stem Cell. 2008 Jul 3;3(1):99-108. doi: 10.1016/j.stem.2008.06.004.
Elucidating the mechanisms underlying hematopoietic stem cell (HSC) specification and expansion in the embryo has been hampered by the lack of analytical cell culture systems that recapitulate in vivo development. Here, we describe an ex vivo model that facilitates a rapid and robust emergence of multipotent long-term repopulating HSCs in the embryonic AGM region. Because this method includes a cell dissociation step prior to reconstruction of a three-dimensional functional tissue and preserves both stromal and hematopoietic elements, it allowed us to identify the direct ancestry of the rapidly expanding HSC pool. We demonstrate that extensive generation of definitive HSCs in the AGM occurs predominantly through the acquisition of stem characteristics by the VE-cadherin+CD45+ population.
由于缺乏能够重现体内发育过程的分析性细胞培养系统,阐明胚胎中造血干细胞(HSC)特化和扩增的潜在机制受到了阻碍。在此,我们描述了一种体外模型,该模型有助于在胚胎主动脉-性腺-中肾(AGM)区域快速且强劲地产生多能长期重建HSC。因为该方法在重建三维功能组织之前包括一个细胞解离步骤,并保留了基质和造血成分,所以它使我们能够确定快速扩增的HSC库的直接谱系。我们证明,AGM中确定性HSC的大量产生主要是通过VE-钙黏蛋白+CD45+群体获得干细胞特征而发生的。