Sato H, Fujiwara M, Bannai S
Department of Biochemistry, Tsukuba University Medical School, Ibaraki, Japan.
J Leukoc Biol. 1992 Aug;52(2):161-4. doi: 10.1002/jlb.52.2.161.
The transport activity of arginine in mouse peritoneal macrophages was strongly induced when they were cultured with 1 ng/ml bacterial lipopolysaccharide (LPS) for 12 h. Arginine in the medium decreased whereas ornithine in the medium increased during the culture. This time-dependent change of arginine to ornithine was accelerated by LPS. However, the activity of arginase in the macrophages did not change during the culture with or without LPS and release of arginase from the cells to the medium was not detected. It is suggested that the transport of arginine and ornithine was a rate-limiting step in arginine-to-ornithine conversion in the macrophage culture medium. A possible role of the induction of arginine transport activity in the macrophage cytocidal activity due to arginine depletion and nitric oxide production is discussed.
当小鼠腹腔巨噬细胞与1 ng/ml细菌脂多糖(LPS)一起培养12小时时,精氨酸的转运活性被强烈诱导。培养过程中,培养基中的精氨酸减少,而鸟氨酸增加。LPS加速了精氨酸向鸟氨酸这种随时间的变化。然而,在有或没有LPS培养期间,巨噬细胞中精氨酸酶的活性没有变化,并且未检测到精氨酸酶从细胞释放到培养基中。提示精氨酸和鸟氨酸的转运是巨噬细胞培养基中精氨酸向鸟氨酸转化的限速步骤。讨论了由于精氨酸消耗和一氧化氮产生,精氨酸转运活性诱导在巨噬细胞杀细胞活性中的可能作用。