Rais M, Wild J S, Choudhury B K, Alam R, Stafford S, Dharajiya N, Sur S
Department of Internal Medicine, Division of Allergy and Immunology, University of Texas Medical Branch, Galveston, Texas 77555, USA.
Clin Exp Allergy. 2002 Apr;32(4):627-32. doi: 10.1046/j.0954-7894.2002.01350.x.
Intrapulmonary administration of IL-12 has been shown to inhibit the number of eosinophils in lung murine models of asthma, but the precise mechanism of this inhibition has not been reported. The purpose of this study was to examine whether IL-12 treatment inhibits bone marrow eosinophilopoiesis, and to elucidate the role of IFN-gamma in this process.
To elucidate the in vivo and in vitro effects of IL-12 on eosinophil differentiation from murine bone marrow (BM) stem cells, and to examine the mechanistic role of IFN-gamma in this process.
Allergen-sensitized BALB/c mice were administered low doses of intranasal IL-12 at the time of allergen challenge, and the number of eosinophils in BM was determined 3 days later. The direct actions of IL-12 on eosinophil differentiation from BM cells were determined in vitro. The mechanistic role of IFN-gamma was assessed by measuring IFN-gamma induction by IL-12 in BM cell cultures, and through the use of IFN-gamma KO mice.
Treatment of allergic mice with intrapulmonary IL-12 (1 ng or 10 ng) reduced eosinophils in BM by 43%. Culture of BM cells from allergen-sensitized mice with IL-3 + IL-5 induced eosinophil differentiation in vitro. Addition of IL-12 to these cultures inhibited eosinophil differentiation, with maximal inhibition (45%) occurring at 10 ng/mL IL-12 concentration. IL-12 induced IFN-gamma production from BM cultures, and failed to inhibit eosinophil differentiation in IFN-gamma-knockout mice, indicating a critical mechanistic role for IFN-gamma.
This study demonstrates that IL-12 selectively inhibits BM eosinophilopoiesis, and that this effect is mediated by IFN-gamma. Intrapulmonary IL-12 has suppressive effects on BM eosinophilopoiesis that may represent a novel mechanism contributing to the anti-eosinophilic effects of IL-12 in allergic airway disease.
在哮喘小鼠肺部模型中,经肺内给予白细胞介素-12(IL-12)已显示可抑制嗜酸性粒细胞数量,但这种抑制的确切机制尚未见报道。本研究的目的是检测IL-12治疗是否抑制骨髓嗜酸性粒细胞生成,并阐明γ干扰素(IFN-γ)在此过程中的作用。
阐明IL-12对小鼠骨髓(BM)干细胞嗜酸性粒细胞分化的体内和体外作用,并检测IFN-γ在此过程中的机制性作用。
在变应原激发时,给变应原致敏的BALB/c小鼠经鼻给予低剂量的IL-12,3天后测定骨髓中嗜酸性粒细胞数量。在体外确定IL-12对骨髓细胞嗜酸性粒细胞分化的直接作用。通过检测BM细胞培养物中IL-12诱导的IFN-γ生成,并使用IFN-γ基因敲除小鼠,评估IFN-γ的机制性作用。
用肺内IL-12(1纳克或10纳克)治疗变应性小鼠可使骨髓中的嗜酸性粒细胞减少43%。用IL-3 + IL-5培养变应原致敏小鼠的BM细胞可在体外诱导嗜酸性粒细胞分化。向这些培养物中添加IL-12可抑制嗜酸性粒细胞分化,在IL-12浓度为10纳克/毫升时抑制作用最大(45%)。IL-12可诱导BM培养物产生IFN-γ,且在IFN-γ基因敲除小鼠中不能抑制嗜酸性粒细胞分化,表明IFN-γ起关键机制性作用。
本研究表明,IL-12选择性抑制骨髓嗜酸性粒细胞生成,且这种作用由IFN-γ介导。肺内IL-12对骨髓嗜酸性粒细胞生成具有抑制作用,这可能是IL-12在变应性气道疾病中产生抗嗜酸性粒细胞作用的一种新机制。