Fujita H, Takahashi S, Okabe S
Department of Applied Pharmacology, Kyoto Pharmaceutical University, Japan.
J Physiol Pharmacol. 1997 Dec;48(4):761-74.
The gastric mucosa of normal rats exhibits no detectable inflammation or visible damage. We examined the effect of the gastric mucosal extract of rats on neutrophil chemotaxis and tried to purify antichemotactic factor. The chemotaxis of neutrophils was examined by the modified Boyden's method. After mucosal layer was scraped and then homogenized and centrifuged at 20,000 x g for 30 min, the supernatant was used as rat gastric mucosal extract (RGME). Prior exposure of neutrophils to the gastric mucosal extract caused a dose-dependent reduction in the neutrophil migration induced by formyl-methionyl-leucyl-phenylalanine (FMLP), leukotriene B4 (LTB4) and interleukin 8 (IL-8) without affecting the cell viability. The antichemotactic factor was partially purified by lectin affinity chromatography on wheat germ lectin (WGL)-Sepharose, anion exchange chromatography on Mono-Q and gel filtration on Superose 12. The molecular weight of the antichemotactic factor was estimated to be around 60 k by gel filtration. The activity was markedly abolished by boiling for 5 min, heating at 60 degrees C for 30 min, and treatment with 1% acetic acid, 0.1 M Na2CO3 or trypsin. Furthermore, the FMLP-induced migration of neutrophils pretreated with the antichemotactic factor for 5 min followed by washing with fresh medium was inhibited, although the factor was not added to the chamber. These results suggest that the gastric mucosa of rats intrinsically generates an antichemotactic factor which might play a crucial role in maintenance of the integrity of the gastric mucosa.
正常大鼠的胃黏膜未表现出可检测到的炎症或可见损伤。我们研究了大鼠胃黏膜提取物对中性粒细胞趋化性的影响,并试图纯化抗趋化因子。采用改良的博伊登方法检测中性粒细胞的趋化性。刮取黏膜层,然后匀浆并在20,000×g下离心30分钟,上清液用作大鼠胃黏膜提取物(RGME)。中性粒细胞预先暴露于胃黏膜提取物会导致由甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)、白三烯B4(LTB4)和白细胞介素8(IL-8)诱导的中性粒细胞迁移呈剂量依赖性降低,且不影响细胞活力。通过在麦胚凝集素(WGL)-琼脂糖上进行凝集素亲和层析、在Mono-Q上进行阴离子交换层析以及在Superose 12上进行凝胶过滤,对抗趋化因子进行了部分纯化。通过凝胶过滤估计抗趋化因子的分子量约为60k。煮沸5分钟、60℃加热30分钟以及用1%乙酸、0.1M碳酸钠或胰蛋白酶处理后,活性明显丧失。此外,用抗趋化因子预处理中性粒细胞5分钟,然后用新鲜培养基洗涤,尽管未向小室中添加该因子,但FMLP诱导的中性粒细胞迁移仍受到抑制。这些结果表明,大鼠胃黏膜内源性产生一种抗趋化因子,该因子可能在维持胃黏膜完整性方面发挥关键作用。