Cohen-Barak Orit, Erickson Drew T, Badowski Michael S, Fuchs Deborah A, Klassen Christine L, Harris David T, Brilliant Murray H
Department of Pediatrics, University of Arizona, College of Medicine, Tucson, AZ 85724, USA.
Exp Hematol. 2007 Mar;35(3):358-67. doi: 10.1016/j.exphem.2006.11.009.
Sox6, a member of the Sox transcription factor family, is essential for the silencing of epsilon y globin gene expression in definitive erythropoiesis of mice. Homozygous Sox6-null mice are neonatally lethal, precluding analysis at later stages. We created adult mice that are deficient in Sox6 specifically in hematopoietic tissues by transplanting embryonic liver stem cells from Sox6-deficient mice into lethally irradiated congenic wild-type adult mice. The mice receiving mutant stem cells (mutant engrafted) showed high expression levels of epsilon y in bone marrow, spleen, and circulating blood compared with mice receiving wild-type and heterozygous stem cells (control engrafted). The level of expression of epsilon y in circulating blood was directly correlated with the percentage of successful mutant donor cell engraftment. Additionally, the mutant engrafted adult mice showed an increase in erythroid precursor cells in bone marrow, spleen, and blood. Thus, Sox6 continues to function as a major regulator of epsilon y in adult definitive erythropoiesis and is required for normal erythrocyte maturation. Therefore, Sox6 may provide a novel therapeutic target by reactivating epsilon y in patients with hemoglobinopathies such as sickle cell anemia and beta-thalassemia.
Sox6是Sox转录因子家族的成员之一,在小鼠定型红细胞生成过程中,对于εy珠蛋白基因表达的沉默至关重要。纯合Sox6基因敲除小鼠在出生时即死亡,这使得无法在后期阶段进行分析。我们通过将来自Sox6缺陷小鼠的胚胎肝干细胞移植到经致死剂量照射的同基因野生型成年小鼠体内,培育出了造血组织特异性缺乏Sox6的成年小鼠。与接受野生型和杂合干细胞(对照移植)的小鼠相比,接受突变干细胞(突变体移植)的小鼠在骨髓、脾脏和循环血液中显示出较高水平的εy表达。循环血液中εy的表达水平与突变供体细胞成功植入的百分比直接相关。此外,突变体移植的成年小鼠在骨髓、脾脏和血液中的红系前体细胞数量增加。因此,Sox6在成年定型红细胞生成过程中继续作为εy的主要调节因子发挥作用,并且是正常红细胞成熟所必需的。因此,Sox6可能通过在镰状细胞贫血和β地中海贫血等血红蛋白病患者中重新激活εy,提供一个新的治疗靶点。