Mori S, Goto K, Goto F, Murakami K, Ohkawara S, Yoshinaga M
Department of Pathology, Kumamoto University School of Medicine, Japan.
Int Immunol. 1994 Jan;6(1):149-56. doi: 10.1093/intimm/6.1.149.
To examine RNA/protein synthesis of neutrophils and related dynamic changes during the inflammatory process, we investigated mRNA expressions in neutrophils, by RNA blot hybridization analyses using 12 different rabbit gene probes. We first selected five candidate genes encoding inflammation-related proteins, i.e. tumor necrosis factor (TNF-alpha) IL-1 alpha, IL-1 beta, neutrophil activating peptide-1/IL-8 (NAP-1/IL-8) and monocyte chemoattractant protein (MCP)-1. We further selected several genes on basis of the results from gene subtraction between cDNA libraries from neutrophils at an early (5 h) and at a late (24 h) stage of casein-induced acute peritonitis in rabbits, i.e. immune activation gene-2 (Act-2), migration inhibitory factor-related protein-8 (MRP-8), MRP-14, gamma-actin, and formyl-methionyl-leucyl-phenylalanine receptor (fMLP-R), and ferritin light (L) chain. In addition to these genes we used ferritin heavy (H) chain gene, another component of the ferritin molecule. We examined mRNA expressions by cytoplasmic slot blot analysis of the above 12 genes in neutrophils obtained from blood and from various stages of casein-induced inflammation in rabbits. The observed patterns of mRNA expression kinetics were classified into three. Pattern 1: mRNAs of MRP-8, MRP-14, and gamma-actin were constitutively expressed in blood neutrophils, and increased rapidly after emigration into inflammatory sites. Pattern 2: mRNAs of IL-1 beta, NAP-1/IL-8, Act-2, and fMLP-R were undetectable in blood neutrophils, and were induced rapidly after the onset of inflammation. Pattern 3 mRNAs of ferritin L and H chain were induced slowly, and increased with progression of the inflammatory process.(ABSTRACT TRUNCATED AT 250 WORDS)
为了研究中性粒细胞的RNA/蛋白质合成以及炎症过程中的相关动态变化,我们使用12种不同的兔基因探针,通过RNA印迹杂交分析,研究了中性粒细胞中的mRNA表达。我们首先选择了五个编码炎症相关蛋白的候选基因,即肿瘤坏死因子(TNF-α)、白细胞介素-1α(IL-1α)、白细胞介素-1β(IL-1β)、中性粒细胞激活肽-1/白细胞介素-8(NAP-1/IL-8)和单核细胞趋化蛋白(MCP)-1。我们还根据兔酪蛋白诱导的急性腹膜炎早期(5小时)和晚期(24小时)中性粒细胞cDNA文库之间基因消减的结果,进一步选择了几个基因,即免疫激活基因-2(Act-2)、迁移抑制因子相关蛋白-8(MRP-8)、MRP-14、γ-肌动蛋白、甲酰甲硫氨酰亮氨酰苯丙氨酸受体(fMLP-R)和铁蛋白轻链。除了这些基因,我们还使用了铁蛋白重链基因,它是铁蛋白分子的另一个组成部分。我们通过细胞质狭缝印迹分析,检测了从血液以及兔酪蛋白诱导炎症不同阶段获得的中性粒细胞中上述12个基因的mRNA表达。观察到的mRNA表达动力学模式分为三类。模式1:MRP-8、MRP-14和γ-肌动蛋白的mRNA在血液中性粒细胞中组成性表达,并在迁移到炎症部位后迅速增加。模式2:白细胞介素-1β、NAP-1/IL-8、Act-2和fMLP-R的mRNA在血液中性粒细胞中未检测到,炎症开始后迅速诱导产生。模式3:铁蛋白轻链和重链的mRNA诱导缓慢,并随着炎症过程的进展而增加。(摘要截断于250字)