Driscoll K E, Hassenbein D G, Howard B W, Isfort R J, Cody D, Tindal M H, Suchanek M, Carter J M
Procter & Gamble Company, Miami Valley Laboratories, Cincinnati, Ohio 45253-8707, USA.
J Leukoc Biol. 1995 Sep;58(3):359-64. doi: 10.1002/jlb.58.3.359.
Macrophage inflammatory protein-2 (MIP-2) is a member of a family of cytokines that play roles in inflammatory, immune, and wound healing responses. To clone the cDNA for rat MIP-2, RNA was isolated from the lungs of Fischer 344 rats after instillation of lipopolysaccharide. Reverse transcription-polymerase chain reaction was performed by using synthetic oligonucleotide primers designed from the mouse MIP-2 cDNA sequence. A cDNA containing the coding region of rat MIP-2 was cloned and sequenced. Comparison to the mouse MIP-2 cDNA demonstrated 90.3% homology at the nucleotide level and 86% homology at the amino acid level. The rat MIP-2 cDNA was expressed in Escherichia coli and protein evaluated for bioactivity. The recombinant rat MIP-2 was chemotactic for rat neutrophils but did not stimulate migration of rat alveolar macrophages or human peripheral blood eosinophils or lymphocytes. In addition, the recombinant rat MIP-2 and the related rat chemokine, KC/CINC stimulated proliferation of rat alveolar epithelial cells but not fibroblasts in vitro.
巨噬细胞炎性蛋白-2(MIP-2)是细胞因子家族的一员,在炎症、免疫和伤口愈合反应中发挥作用。为了克隆大鼠MIP-2的cDNA,在向Fischer 344大鼠肺部注入脂多糖后,从其肺中分离出RNA。使用根据小鼠MIP-2 cDNA序列设计的合成寡核苷酸引物进行逆转录-聚合酶链反应。克隆并测序了包含大鼠MIP-2编码区的cDNA。与小鼠MIP-2 cDNA比较显示,在核苷酸水平上同源性为90.3%,在氨基酸水平上同源性为86%。大鼠MIP-2 cDNA在大肠杆菌中表达,并对表达的蛋白质进行生物活性评估。重组大鼠MIP-2对大鼠中性粒细胞具有趋化作用,但不刺激大鼠肺泡巨噬细胞、人外周血嗜酸性粒细胞或淋巴细胞的迁移。此外,重组大鼠MIP-2和相关的大鼠趋化因子KC/CINC在体外可刺激大鼠肺泡上皮细胞增殖,但不刺激成纤维细胞增殖。