Gazit Roi, Mandal Pankaj K, Ebina Wataru, Ben-Zvi Ayal, Nombela-Arrieta César, Silberstein Leslie E, Rossi Derrick J
Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138 Program in Cellular and Molecular Medicine, Division of Hematology/Oncology and Division of Transfusion Medicine, Department of Laboratory Medicine, Boston Children's Hospital, MA 02116.
Department of Pediatrics, Department of Neurobiology, Harvard Medical School, Boston MA 02115.
J Exp Med. 2014 Jun 30;211(7):1315-31. doi: 10.1084/jem.20130428. Epub 2014 Jun 23.
Hematopoietic stem cells (HSCs) are the best-characterized tissue-specific stem cells, yet experimental study of HSCs remains challenging, as they are exceedingly rare and methods to purify them are cumbersome. Moreover, genetic tools for specifically investigating HSC biology are lacking. To address this we sought to identify genes uniquely expressed in HSCs within the hematopoietic system and to develop a reporter strain that specifically labels them. Using microarray profiling we identified several genes with HSC-restricted expression. Generation of mice with targeted reporter knock-in/knock-out alleles of one such gene, Fgd5, revealed that though Fgd5 was required for embryonic development, it was not required for definitive hematopoiesis or HSC function. Fgd5 reporter expression near exclusively labeled cells that expressed markers consistent with HSCs. Bone marrow cells isolated based solely on Fgd5 reporter signal showed potent HSC activity that was comparable to stringently purified HSCs. The labeled fraction of the Fgd5 reporter mice contained all HSC activity, and HSC-specific labeling was retained after transplantation. Derivation of next generation mice bearing an Fgd5-CreERT2 allele allowed tamoxifen-inducible deletion of a conditional allele specifically in HSCs. In summary, reporter expression from the Fgd5 locus permits identification and purification of HSCs based on single-color fluorescence.
造血干细胞(HSCs)是特征最明确的组织特异性干细胞,但对造血干细胞的实验研究仍然具有挑战性,因为它们极其罕见,且纯化方法繁琐。此外,缺乏专门用于研究造血干细胞生物学的遗传工具。为了解决这一问题,我们试图在造血系统中鉴定在造血干细胞中独特表达的基因,并开发一种能特异性标记它们的报告菌株。通过微阵列分析,我们鉴定出了几个具有造血干细胞限制性表达的基因。利用其中一个这样的基因Fgd5,生成带有靶向报告基因敲入/敲除等位基因的小鼠,结果显示,虽然Fgd5是胚胎发育所必需的,但它对于定型造血或造血干细胞功能并非必需。Fgd5报告基因表达几乎只标记了表达与造血干细胞一致标志物的细胞。仅基于Fgd5报告基因信号分离的骨髓细胞显示出强大的造血干细胞活性,与严格纯化的造血干细胞相当。Fgd5报告基因小鼠的标记部分包含了所有造血干细胞活性,并且移植后仍保留了造血干细胞特异性标记。携带Fgd5-CreERT2等位基因的下一代小鼠的衍生,使得他莫昔芬诱导的条件等位基因在造血干细胞中特异性缺失。总之,来自Fgd5基因座的报告基因表达允许基于单色荧光对造血干细胞进行鉴定和纯化。