Dybedal I, Larsen S, Jacobsen S E
Institute of Cancer Research, University of Trondheim, Norway.
J Immunol. 1995 May 15;154(10):4950-5.
It has been demonstrated recently that in vivo administration of murine IL-12 to mice enhances the activity of cytotoxic NK cells and lymphocyte-activated killer cells, and that it has antitumor and antimetastatic activity. However, one side effect observed in response to systemic IL-12 treatment is anemia. In the present study, we examined for the first time the ability of IL-12 to affect directly the growth of murine erythroid progenitor cells in vitro. Whereas IL-12 alone or in combination with Erythropoietin (Epo) showed no stimulatory effect on erythroid progenitors, IL-12 potently enhanced the number of erythroid burst-forming unit (BFU-E) colonies formed in response to Epo+IL-4 by 63% and Epo+stem cell factor by 80%. The stimulatory effect of IL-12 occurred in a concentration-dependent fashion, with maximum enhancing effect observed at 50 ng/ml. Furthermore, single cell experiments suggested that the stimulatory effect of IL-12 on erythroid colony formation was directly mediated. Thus, IL-12 can directly enhance murine erythropoiesis in vitro, suggesting that IL-12-induced anemia is mediated through an indirect mechanism.
最近有研究表明,给小鼠体内注射鼠白细胞介素-12(IL-12)可增强细胞毒性自然杀伤(NK)细胞和淋巴细胞激活的杀伤细胞的活性,且具有抗肿瘤和抗转移活性。然而,全身应用IL-12治疗时观察到的一个副作用是贫血。在本研究中,我们首次检测了IL-12在体外直接影响小鼠红系祖细胞生长的能力。单独使用IL-12或与促红细胞生成素(Epo)联合使用时,对红系祖细胞均无刺激作用,但IL-12能使Epo+IL-4诱导形成的红系爆式集落形成单位(BFU-E)集落数量显著增加63%,使Epo+干细胞因子诱导形成的BFU-E集落数量显著增加80%。IL-12的刺激作用呈浓度依赖性,在50 ng/ml时增强效果最为明显。此外,单细胞实验表明IL-12对红系集落形成的刺激作用是直接介导的。因此,IL-12可在体外直接增强小鼠红细胞生成,提示IL-12诱导的贫血是通过间接机制介导的。