Departments of Biology and Computing and Mathematical Sciences, California Institute of Technology, Pasadena, CA 91125, USA.
Proc Natl Acad Sci U S A. 2012 Mar 13;109(11):4233-8. doi: 10.1073/pnas.1200677109. Epub 2012 Feb 24.
MicroRNA-125b (miR-125b) is up-regulated in patients with leukemia. Overexpression of miR-125b alone in mice causes a very aggressive, transplantable myeloid leukemia. Before leukemia, these mice do not display elevation of white blood cells in the spleen or bone marrow; rather, the hematopoietic compartment shows lineage-skewing, with myeloid cell numbers dramatically increased and B-cell numbers severely diminished. miR-125b exerts this effect by up-regulating the number of common myeloid progenitors while inhibiting development of pre-B cells. We applied a miR-125b sponge loss of function system in vivo to show that miR-125b physiologically regulates hematopoietic development. Investigating the mechanism by which miR-125b regulates hematopoiesis, we found that, among a panel of candidate targets, the mRNA for Lin28A, an induced pluripotent stem cell gene, was most repressed by miR-125b in mouse hematopoietic stem and progenitor cells. Overexpressing Lin28A in the mouse hematopoietic system mimicked the phenotype observed on inhibiting miR-125b function, leading to a decrease in hematopoietic output. Relevant to the miR-125b overexpression phenotype, we also found that knockdown of Lin28A led to hematopoietic lineage-skewing, with increased myeloid and decreased B-cell numbers. Thus, the miR-125b target Lin28A is an important regulator of hematopoiesis and a primary target of miR-125b in the hematopoietic system.
MicroRNA-125b (miR-125b) 在白血病患者中上调。单独在小鼠中过表达 miR-125b 会导致一种非常侵袭性的、可移植的髓性白血病。在白血病之前,这些小鼠的脾脏或骨髓中没有白细胞升高;相反,造血细胞表现出谱系偏倚,髓系细胞数量显著增加,B 细胞数量严重减少。miR-125b 通过上调共同髓系祖细胞的数量,同时抑制前 B 细胞的发育,发挥这种作用。我们在体内应用 miR-125b 海绵失活系统,表明 miR-125b 生理上调节造血发育。在研究 miR-125b 调节造血的机制时,我们发现,在一组候选靶标中,Lin28A 的 mRNA,一种诱导多能干细胞基因,在小鼠造血干细胞和祖细胞中被 miR-125b 抑制的程度最高。在小鼠造血系统中过表达 Lin28A 模拟了抑制 miR-125b 功能所观察到的表型,导致造血输出减少。与 miR-125b 过表达表型相关,我们还发现,Lin28A 的敲低导致造血谱系偏倚,髓系细胞数量增加,B 细胞数量减少。因此,miR-125b 的靶标 Lin28A 是造血的重要调节因子,也是 miR-125b 在造血系统中的主要靶标。