Sainteny F, Larras-Regard E, Frindel E
Cellular Kinetics Research Unit, INSERM U250, Gustave-Roussy Institute, Villejuif, France.
Exp Cell Res. 1990 Mar;187(1):174-6. doi: 10.1016/0014-4827(90)90133-u.
We have previously reported that E pluripoietins are produced in mice after a single 20-mg injection of cytosine arabinoside (Ara-C) and that they are able to initiate the determination of hemopoietic pluripotent stem cells (CFU-S) toward the erythrocytic lineage. However, the mechanism of E pluripoietin release is still unclear. Since the stimulating effect of thyroid hormone on erythropoiesis is well known, we postulated a link between this hormone and the E pluripoietins. In previous papers we demonstrated that L-triiodothyronine (LT3) exhibits the capacity of inducing CFU-S differentiation toward erythropoiesis in vitro. Two series of data presented here suggest that LT3 acts indirectly on CFU-S determination by promoting the release of E pluripoietin-like factors. First, the Ara-C injection which induces the production of E pluripoietins in mice also promotes an increase in the LT3 plasma level. Second, medium conditioned with bone marrow cells exposed in vitro for 90 min to LT3 (even though this medium does not contain LT3) has E pluripoietin-like effects, inducing CFU-S differentiation toward the erythrocytic lineage.
我们之前曾报道,单次注射20毫克阿糖胞苷(Ara-C)后,小鼠体内会产生E多能素,且它们能够启动造血多能干细胞(CFU-S)向红细胞谱系的定向分化。然而,E多能素的释放机制仍不清楚。鉴于甲状腺激素对红细胞生成的刺激作用是众所周知的,我们推测这种激素与E多能素之间存在联系。在之前的论文中,我们证明了L-三碘甲状腺原氨酸(LT3)在体外具有诱导CFU-S向红细胞生成分化的能力。此处呈现的两组数据表明,LT3通过促进E多能素样因子的释放,间接作用于CFU-S的定向分化。首先,在小鼠体内诱导产生E多能素的阿糖胞苷注射,也会促使LT3血浆水平升高。其次,用体外暴露于LT3 90分钟的骨髓细胞培养的培养基(即使该培养基不含LT3)具有E多能素样效应,可诱导CFU-S向红细胞谱系分化。