Izutani R, Ohyanagi H, MacDermott R P
Second Department of Surgery, Kinki University School of Medicine, Osaka, Japan.
Microbiol Immunol. 1994;38(3):233-7. doi: 10.1111/j.1348-0421.1994.tb01770.x.
A quantitative polymerase chain reaction (PCR) assay for mRNA expression of interleukin-8 (IL-8), a neutrophil chemotactant and activator, was developed to examine the expression of this cytokine by colonic mucosa. A synthetic IL-8 RNA deleted in size of native IL-8 mRNA was used as an external control. The synthetic IL-8 RNA was mixed with total RNA from cells and converted to cDNA and amplified by PCR simultaneously. The lower limit of sensitivity for the assay was found to be more than 1 femtogram of IL-8 mRNA. The assay determined IL-8 mRNA expression when the RNA was isolated from either human histiocytic lymphoma cell line U937 cells or human colonic mucosa obtained from colitis patients and healthy controls. The development of the rapid and sensitive assay should provide a means to more fully evaluate the role of this cytokine in diverse disease states with small scale.
为检测结肠黏膜中白细胞介素-8(IL-8,一种中性粒细胞趋化剂和激活剂)的细胞因子表达,开发了一种用于白细胞介素-8 mRNA表达的定量聚合酶链反应(PCR)检测方法。一种在天然IL-8 mRNA大小上缺失的合成IL-8 RNA用作外部对照。将合成IL-8 RNA与细胞总RNA混合,转化为cDNA并同时通过PCR扩增。该检测方法的灵敏度下限为超过1飞克的IL-8 mRNA。当从人组织细胞淋巴瘤细胞系U937细胞或从结肠炎患者和健康对照获得的人结肠黏膜中分离RNA时,该检测方法可测定IL-8 mRNA表达。这种快速灵敏检测方法的开发应提供一种手段,以便在小规模情况下更全面地评估这种细胞因子在多种疾病状态中的作用。