Rothenberg M E, Luster A D, Lilly C M, Drazen J M, Leder P
Howard Hughes Medical Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115.
J Exp Med. 1995 Mar 1;181(3):1211-6. doi: 10.1084/jem.181.3.1211.
Eotaxin is a member of the C-C family of chemokines and is related during antigen challenge in a guinea pig model of allergic airway inflammation (asthma). Consistent with its putative role in eosinophilic inflammation, eotaxin induces the selective infiltration of eosinophils when injected into the lung and skin. Using a guinea pig lung cDNA library, we have cloned full-length eotaxin cDNA. The cDNA encodes a protein of 96 amino acids, including a putative 23-amino acid hydrophobic leader sequence, followed by 73 amino acids composing the mature active eotaxin protein. The protein-coding region of this cDNA is 73, 71, 50, and 48% identical in nucleic acid sequence to those of human macrophage chemoattractant protein (MCP) 3, MCP-1, macrophage inflammatory protein (MIP) 1 alpha, and RANTES, respectively. Analysis of genomic DNA suggested that there is a single eotaxin gene in guinea pig which is apparently conserved in mice. High constitutive levels of eotaxin mRNA expression were observed in the lung, while the intestines, stomach, spleen, liver, heart, thymus, testes, and kidney expressed lower levels. To determine if eotaxin mRNA levels are elevated during allergen-induced eosinophilic airway inflammation, ovalbumin (OVA)-sensitized guinea pigs were challenged with aerosolized antigen. Compared with the lungs from saline-challenged animals, eotaxin mRNA levels increased sixfold within 3 h and returned to baseline by 6 h. Thus, eotaxin mRNA levels are increased in response to allergen challenge during the late phase response. The identification of constitutive eotaxin mRNA expression in multiple tissues suggests that in addition to regulating airway eosinophilia, eotaxin is likely to be involved in eosinophil recruitment into other tissues as well as in baseline tissue homing.
嗜酸性粒细胞趋化因子是C-C趋化因子家族的一员,在豚鼠过敏性气道炎症(哮喘)模型的抗原激发过程中发挥作用。与其在嗜酸性粒细胞炎症中假定的作用一致,将嗜酸性粒细胞趋化因子注入肺和皮肤时,它会诱导嗜酸性粒细胞的选择性浸润。利用豚鼠肺cDNA文库,我们克隆了全长嗜酸性粒细胞趋化因子cDNA。该cDNA编码一个96个氨基酸的蛋白质,包括一个假定的23个氨基酸的疏水前导序列,随后是由73个氨基酸组成的成熟活性嗜酸性粒细胞趋化因子蛋白。该cDNA的蛋白质编码区与人类巨噬细胞趋化蛋白(MCP)3、MCP-1、巨噬细胞炎性蛋白(MIP)1α和调节激活正常T细胞表达和分泌因子(RANTES)的核酸序列分别有73%、71%、50%和48%的同源性。基因组DNA分析表明,豚鼠中有一个单一的嗜酸性粒细胞趋化因子基因,该基因在小鼠中显然是保守的。在肺中观察到嗜酸性粒细胞趋化因子mRNA的高组成性表达水平,而肠道、胃、脾脏、肝脏、心脏、胸腺、睾丸和肾脏中的表达水平较低。为了确定在变应原诱导的嗜酸性粒细胞气道炎症过程中嗜酸性粒细胞趋化因子mRNA水平是否升高,用卵清蛋白(OVA)致敏的豚鼠接受雾化抗原激发。与盐水激发动物的肺相比,嗜酸性粒细胞趋化因子mRNA水平在3小时内增加了6倍,并在6小时内恢复到基线水平。因此,在迟发相反应期间,嗜酸性粒细胞趋化因子mRNA水平会因变应原激发而升高。在多个组织中鉴定出组成性嗜酸性粒细胞趋化因子mRNA表达表明,除了调节气道嗜酸性粒细胞增多外,嗜酸性粒细胞趋化因子可能还参与嗜酸性粒细胞向其他组织的募集以及基线组织归巢。