Minshall E M, Schleimer R, Cameron L, Minnicozzi M, Egan R W, Gutierrez-Ramos J C, Eidelman D H, Hamid Q
Meakins-Christie Laboratories and Montreal Chest Institute Research Center, McGill University, Montreal, Canada.
Am J Respir Crit Care Med. 1998 Sep;158(3):951-7. doi: 10.1164/ajrccm.158.3.9709114.
Interleukin-5 (IL-5) is a potent eosinophilopoietic factor implicated in the chronic inflammatory cell accumulation accompanying bronchial asthma. However, its role in stimulating eosinophil differentiation within the bone marrow following allergen exposure remains to be elucidated. The aims of our study were to determine the expression of IL-5 within the bone marrow of sensitized and control mice after allergen exposure, and to investigate the cellular phenotype of IL-5-producing cells. Sensitized Balb/c mice were challenged with either ovalbumin (OVA) or sterile saline. After 6 h, the mice were exsanguinated and the bone marrow prepared for cytospins. Bone marrow-derived cells from OVA-sensitized mice exhibited an increase in IL-5 immunoreactivity and mRNA compared with those from nonsensitized control mice (p < 0. 05). After allergen challenge, there was a further increase in IL-5 expression (p < 0.05) within the bone marrow. Both sensitization and allergen challenge resulted in an increase in the number of cells expressing major basic protein (MBP) (p < 0.05). In nonsensitized mice, the IL-5 mRNA was expressed predominantly by CD34-positive (CD34+) progenitor cells. Following sensitization and allergen challenge, CD3-positive (CD3+) T lymphocytes were the major source of this cytokine. These results demonstrate the presence of IL-5 within the bone marrow of normal Balb/c mice. After sensitization and allergen challenge, the increase in IL-5-producing cells within the bone marrow is attributed by T lymphocytes.
白细胞介素-5(IL-5)是一种强效的嗜酸性粒细胞生成因子,与支气管哮喘伴发的慢性炎症细胞积聚有关。然而,其在变应原暴露后刺激骨髓内嗜酸性粒细胞分化中的作用仍有待阐明。我们研究的目的是确定变应原暴露后致敏小鼠和对照小鼠骨髓内IL-5的表达情况,并研究产生IL-5细胞的细胞表型。将致敏的Balb/c小鼠用卵清蛋白(OVA)或无菌生理盐水进行激发。6小时后,处死小鼠并制备骨髓细胞涂片。与未致敏的对照小鼠相比,OVA致敏小鼠的骨髓来源细胞IL-5免疫反应性和mRNA水平升高(p<0.05)。变应原激发后,骨髓内IL-5表达进一步增加(p<0.05)。致敏和变应原激发均导致表达主要碱性蛋白(MBP)的细胞数量增加(p<0.05)。在未致敏小鼠中,IL-5 mRNA主要由CD34阳性(CD34+)祖细胞表达。致敏和变应原激发后,CD3阳性(CD3+)T淋巴细胞是这种细胞因子的主要来源。这些结果表明正常Balb/c小鼠骨髓内存在IL-5。致敏和变应原激发后,骨髓内产生IL-5的细胞增加是由T淋巴细胞引起的。