Fujiwara Y, Higuchi K, Takashima T, Hamaguchi M, Watanabe T, Tominaga K, Oshitani N, Matsumoto T, Arakawa T
Department of Gastroenterology, Osaka City University Graduate School of Medicine, Abeno-ku, Japan.
Aliment Pharmacol Ther. 2002 Apr;16 Suppl 2:52-8. doi: 10.1046/j.1365-2036.16.s2.29.x.
Epidermal growth factor (EGF), which binds to EGF receptors (EGF-R), stimulates oesophageal epithelial cell proliferation, enabling rapid repair after mucosal injury. In the normal human oesophageal epithelium, EGF-R expression is present and confined to the basal layer.
To examine histological changes in and dynamics of EGF-R expression during healing after acid reflux oesophagitis in a rat model.
Gastric acid reflux oesophagitis was induced in Wistar rats by ligation of the pylorus and the transitional region between the forestomach and the grandular portion for 5 h, followed by release of both ligations. Rats were killed 7 and 14 days after production of oesophagitis to examine macroscopic and histological changes as well as dynamics of EGF-R expression. Epithelial cell proliferation was assessed by bromodeoxyuridine (BrdU) uptake, and expression of EGF-R mRNA and protein by RT-PCR and Western blotting or immunohistochemistry.
Gastric acid reflux induced erosive and ulcerative mucosal lesions in the lower and middle part of the oesophagus. These lesions were healed by 14 days and histologically showed thickening of the oesophageal epithelium from 41.11 +/- 3.09 microm in controls to 142.73 +/- 11.59 microm (P < 0.001) in ligated rats, as well as elongation of papillae and basal cell hyperplasia. The number of BrdU-positive cells among basal cells on day 14 was significantly increased from 7.1 +/- 0.8/field in controls to 30.9 +/- 3.0/field in ligated rats. Expression of EGF-R mRNA and protein was significantly increased on day 14 and most basal cells were immunohistochemically positive in both BrdU and EGF-R staining.
Acid reflux-induced oesophageal injury caused basal cell hyperplasia with an increase in cell proliferation and EGF-R expression. Activation of EGF-R gene and protein in response to acid reflux-induced injury may facilitate mucosal healing. These results suggest that epidermal growth factor receptors play a crucial role in healing after acid reflux oesophagitis in rats.
表皮生长因子(EGF)与表皮生长因子受体(EGF-R)结合,刺激食管上皮细胞增殖,使黏膜损伤后能快速修复。在正常人类食管上皮中,存在EGF-R表达且局限于基底层。
在大鼠模型中研究酸反流性食管炎愈合过程中EGF-R表达的组织学变化及其动态情况。
通过结扎Wistar大鼠的幽门以及前胃与腺部之间的过渡区域5小时,随后解除两处结扎来诱导胃酸反流性食管炎。在产生食管炎后7天和14天处死大鼠,以检查宏观和组织学变化以及EGF-R表达的动态情况。通过溴脱氧尿苷(BrdU)摄取评估上皮细胞增殖,通过逆转录聚合酶链反应(RT-PCR)、蛋白质印迹法或免疫组织化学评估EGF-R mRNA和蛋白质的表达。
胃酸反流在食管中下部引起糜烂性和溃疡性黏膜病变。这些病变在14天内愈合,组织学显示食管上皮增厚,对照组为41.11±3.09微米,结扎大鼠为142.73±11.59微米(P<0.001),同时乳头伸长和基底细胞增生。第14天基底层中BrdU阳性细胞数量从对照组的7.1±0.8/视野显著增加到结扎大鼠的30.9±3.0/视野。第14天EGF-R mRNA和蛋白质的表达显著增加,在BrdU和EGF-R染色中大多数基底细胞免疫组化呈阳性。
酸反流引起的食管损伤导致基底细胞增生,细胞增殖和EGF-R表达增加。酸反流诱导的损伤后EGF-R基因和蛋白质的激活可能促进黏膜愈合。这些结果表明表皮生长因子受体在大鼠酸反流性食管炎后的愈合中起关键作用。