Eilken Hanna M, Nishikawa Shin-Ichi, Schroeder Timm
Institute of Stem Cell Research, Helmholtz Center Munich-German Research Center for Environmental Health (GmbH), 85764 Neuherberg, Germany.
Nature. 2009 Feb 12;457(7231):896-900. doi: 10.1038/nature07760.
Despite decades of research, the identity of the cells generating the first haematopoietic cells in mammalian embryos is unknown. Indeed, whether blood cells arise from mesodermal cells, mesenchymal progenitors, bipotent endothelial-haematopoietic precursors or haemogenic endothelial cells remains controversial. Proximity of endothelial and blood cells at sites of embryonic haematopoiesis, as well as their similar gene expression, led to the hypothesis of the endothelium generating blood. However, owing to lacking technology it has been impossible to observe blood cell emergence continuously at the single-cell level, and the postulated existence of haemogenic endothelial cells remains disputed. Here, using new imaging and cell-tracking methods, we show that embryonic endothelial cells can be haemogenic. By continuous long-term single-cell observation of mouse mesodermal cells generating endothelial cell and blood colonies, it was possible to detect haemogenic endothelial cells giving rise to blood cells. Living endothelial and haematopoietic cells were identified by simultaneous detection of morphology and multiple molecular and functional markers. Detachment of nascent blood cells from endothelium is not directly linked to asymmetric cell division, and haemogenic endothelial cells are specified from cells already expressing endothelial markers. These results improve our understanding of the developmental origin of mammalian blood and the potential generation of haematopoietic stem cells from embryonic stem cells.
尽管经过数十年的研究,但哺乳动物胚胎中产生首批造血细胞的细胞身份仍不清楚。实际上,血细胞是源自中胚层细胞、间充质祖细胞、双能内皮-造血前体还是造血内皮细胞,这一问题仍存在争议。胚胎造血部位内皮细胞和血细胞的紧密相邻,以及它们相似的基因表达,引发了内皮细胞产生血液的假说。然而,由于技术限制,一直无法在单细胞水平连续观察血细胞的出现,造血内皮细胞的假定存在也仍有争议。在此,我们使用新的成像和细胞追踪方法表明,胚胎内皮细胞可以是造血的。通过对产生内皮细胞和血细胞集落的小鼠中胚层细胞进行连续长期的单细胞观察,能够检测到产生血细胞的造血内皮细胞。通过同时检测形态以及多种分子和功能标记物来识别活的内皮细胞和造血细胞。新生血细胞从内皮细胞脱离与不对称细胞分裂并无直接关联,造血内皮细胞是由已经表达内皮标记物的细胞特化而来的。这些结果增进了我们对哺乳动物血液发育起源以及从胚胎干细胞产生造血干细胞潜力的理解。