Mahmoud Y A, Harada K, Nagasaki A, Gotoh T, Takeya M, Ueda A, Mori M
Department of Molecular Genetics, Kumamoto University School of Medicine, Kumamoto, 860-0811, Japan.
Nitric Oxide. 1999 Aug;3(4):302-11. doi: 10.1006/niox.1999.0241.
Expression of inducible nitric oxide (NO) synthase (iNOS) and related enzymes of arginine metabolism in the mouse lung exposed to filamentous fungus Fusarium kyushuense was studied by RNA blot, immunoblot, and histological analyses. When mice were exposed intranasally to the fungi only once, no induction of iNOS mRNA was observed. However, when the animals were infected again 6 days after the first exposure, iNOS mRNA was induced, reached a maximum 12-24 h after the exposure, and decreased to an undetectable level at 48 h. mRNAs for cationic amino acid transporter-2 (CAT2) and argininosuccinate synthetase were induced gradually, reached a maximum at 24 h, and decreased at 48 h. Arginase II mRNA increased at 24 h and decreased markedly at 48 h. On the other hand, arginase I mRNA started to increase at 24 h and reached to a much higher level at 48 h. Ornithine decarboxylase and ornithine aminotransferase mRNAs were also induced. Immunoblot analysis showed that iNOS, argininosuccinate synthetase, and arginase I and II proteins were induced with similar kinetics as those of their respective mRNAs. In histological examination, fungal elements were observed in the bronchoalveolar lumen at 3-6 h, decreased at 12 h, and almost disappeared at 48 h. Small granuloma appeared 3 h after the infection and their size increased with time. These results suggest that NO is produced in the mouse lung in response to F. kyushuense exposure and that the NO production is regulated by CAT2, the citrulline-NO cycle, and arginase isoforms. Enhanced synthesis of polyamines and proline (and thus collagen) is also suggested.
通过RNA印迹、免疫印迹和组织学分析,研究了暴露于丝状真菌九州镰孢菌的小鼠肺中诱导型一氧化氮(NO)合酶(iNOS)及精氨酸代谢相关酶的表达情况。当小鼠仅经鼻暴露于真菌一次时,未观察到iNOS mRNA的诱导。然而,当动物在首次暴露6天后再次感染时,iNOS mRNA被诱导,在暴露后12 - 24小时达到最大值,并在48小时降至不可检测水平。阳离子氨基酸转运体-2(CAT2)和精氨酸琥珀酸合成酶的mRNA逐渐被诱导,在24小时达到最大值,并在48小时下降。精氨酸酶II mRNA在24小时增加,并在48小时显著下降。另一方面,精氨酸酶I mRNA在24小时开始增加,并在48小时达到更高水平。鸟氨酸脱羧酶和鸟氨酸转氨酶的mRNA也被诱导。免疫印迹分析表明,iNOS、精氨酸琥珀酸合成酶以及精氨酸酶I和II蛋白的诱导动力学与其各自mRNA的相似。在组织学检查中,在3 - 6小时支气管肺泡腔内观察到真菌成分,12小时减少,48小时几乎消失。感染后3小时出现小肉芽肿,其大小随时间增加。这些结果表明,小鼠肺在暴露于九州镰孢菌后产生NO,并且NO的产生受CAT2、瓜氨酸-NO循环和精氨酸酶同工型的调节。还提示了多胺和脯氨酸(以及因此的胶原蛋白)合成增强。