Kazumori H, Ishihara S, Hoshino E, Kawashima K, Moriyama N, Suetsugu H, Sato H, Adachi K, Fukuda R, Watanabe M, Takasawa S, Okamoto H, Fukui H, Chiba T, Kinoshita Y
Second Department of Internal Medicine, Shimane Medical University, Izumo, Japan.
Gastroenterology. 2000 Dec;119(6):1610-22. doi: 10.1053/gast.2000.20262.
BACKGROUND & AIMS: Regenerating (Reg) protein has a trophic effect on gastric mucosal cells. We have shown that Reg gene expression is increased in enterochromaffin-like (ECL) cells during the healing of damaged gastric mucosa around mucosal erosion. This study was designed to explore the stimulants of Reg expression during the healing of gastric mucosal damage.
Time course changes of the expression of genes for various proinflammatory cytokines and Reg were investigated after induction of gastric mucosal lesions in rats. The direct effect of proinflammatory cytokines on Reg gene expression and Reg protein production were investigated in vitro using counterflow elutriation-enriched rat ECL cells. CXC receptor 2 (CXCR-2) expression was investigated in ECL cells by reverse-transcription polymerase chain reaction. Reg gene expression was also investigated in rats treated by the neutralizing antibody of cytokine-induced neutrophil chemoattractant (CINC-2 beta).
During healing, the gene expression of several proinflammatory cytokines and Reg was markedly augmented. Among the proinflammatory cytokines, CINC-2 beta is the only cytokine in which augmented expression preceded the increase of Reg gene expression. In rats treated with CINC-2 beta neutralizing antibody, the augmentation of Reg gene expression was significantly inhibited. When ECL cells were incubated with these proinflammatory cytokines, CINC-2 beta dose-dependently increased Reg messenger RNA and Reg protein in ECL cells. CXCR-2 was identified in isolated ECL cells.
CINC-2 beta, expressed in damaged gastric mucosa, stimulates the production of Reg protein in ECL cells via CXCR-2 and may be involved in the accelerated healing of injured gastric mucosa.
再生(Reg)蛋白对胃黏膜细胞具有营养作用。我们已经表明,在黏膜糜烂周围受损胃黏膜愈合过程中,Reg基因在肠嗜铬样(ECL)细胞中的表达增加。本研究旨在探讨胃黏膜损伤愈合过程中Reg表达的刺激因素。
在大鼠胃黏膜损伤诱导后,研究各种促炎细胞因子和Reg基因表达的时间进程变化。使用逆流淘析富集的大鼠ECL细胞在体外研究促炎细胞因子对Reg基因表达和Reg蛋白产生的直接影响。通过逆转录聚合酶链反应研究ECL细胞中CXC受体2(CXCR-2)的表达。还在细胞因子诱导的中性粒细胞趋化因子(CINC-2β)中和抗体处理的大鼠中研究Reg基因表达。
在愈合过程中,几种促炎细胞因子和Reg的基因表达明显增强。在促炎细胞因子中,CINC-2β是唯一一种表达增强先于Reg基因表达增加的细胞因子。在用CINC-2β中和抗体处理的大鼠中,Reg基因表达的增强被显著抑制。当ECL细胞与这些促炎细胞因子一起孵育时,CINC-2β剂量依赖性地增加ECL细胞中的Reg信使核糖核酸和Reg蛋白。在分离的ECL细胞中鉴定出CXCR-2。
在受损胃黏膜中表达的CINC-2β通过CXCR-2刺激ECL细胞中Reg蛋白的产生,并可能参与受损胃黏膜的加速愈合。