Ohta Hideaki, Sawada Akihisa, Kim Ji Yoo, Tokimasa Sadao, Nishiguchi Seiji, Humphries R Keith, Hara Junichi, Takihara Yoshihiro
Department of Developmental Biology and Medicine, Osaka Medical Center for Cancer and Cardiovascular Diseases, 3-3 Nakamichi-1, Higashinari, Osaka 537-8511, Japan.
J Exp Med. 2002 Mar 18;195(6):759-70. doi: 10.1084/jem.20011911.
The rae28 gene (rae28), also designated as mph1, is a mammalian ortholog of the Drosophila polyhomeotic gene, a member of Polycomb group genes (PcG). rae28 constitutes PcG complex 1 for maintaining transcriptional states which have been once initiated, presumably through modulation of the chromatin structure. Hematopoietic activity was impaired in the fetal liver of rae28-deficient animals (rae28-/-), as demonstrated by progressive reduction of hematopoietic progenitors of multilineages and poor expansion of colony forming units in spleen (CFU-S(12)) during embryonic development. An in vitro long-term culture-initiating cell assay suggested a reduction in hematopoietic stem cells (HSCs), which was confirmed in vivo by reconstitution experiments in lethally irradiated congenic recipient mice. The competitive repopulating units (CRUs) reflect HSCs supporting multilineage blood-cell production. CRUs were generated, whereas the number of CRUs was reduced by a factor of 20 in the rae28-/- fetal liver. We also performed serial transplantation experiments to semiquantitatively measure self-renewal activity of CRUs in vivo. Self-renewal activity of CRUs was 15-fold decreased in rae28-/-. Thus the compromised HSCs were presumed to reduce hematopoietic activity in the rae28-/- fetal liver. This is the first report to suggest that rae28 has a crucial role in sustaining the activity of HSCs to maintain hematopoiesis.
rae28基因(rae28),也被命名为mph1,是果蝇多同源异型基因在哺乳动物中的直系同源基因,属于多梳蛋白家族基因(PcG)的成员。rae28构成了多梳蛋白复合体1,用于维持曾经启动过的转录状态,可能是通过调节染色质结构来实现的。在rae28基因缺陷动物(rae28-/-)的胎肝中,造血活性受损,这在胚胎发育过程中表现为多谱系造血祖细胞的逐渐减少以及脾脏中集落形成单位(CFU-S(12))的增殖不良。一项体外长期培养起始细胞实验表明造血干细胞(HSC)数量减少,这在经致死性照射的同基因受体小鼠体内的重建实验中得到了证实。竞争性再增殖单位(CRU)反映了支持多谱系血细胞生成的造血干细胞。虽然能产生CRU,但在rae28-/-胎肝中CRU的数量减少了20倍。我们还进行了系列移植实验,以半定量地测量体内CRU的自我更新活性。在rae28-/-中,CRU的自我更新活性降低了15倍。因此,推测受损的造血干细胞会降低rae28-/-胎肝中的造血活性。这是首份表明rae28在维持造血干细胞活性以维持造血过程中起关键作用的报告。