Kawai Y, Akagawa K
Department of Bacteriology, National Institute of Health, Tokyo, Japan.
Infect Immun. 1989 Jul;57(7):2086-91. doi: 10.1128/iai.57.7.2086-2091.1989.
alpha-N-(3-Acyloxyacyl)-ornithine (or -serine) is the structure of lipoamino acids obtained by us previously from some gram-negative bacteria (Y. Kawai and I. Yano, Eur. J. Biochem. 136:531-538, 1983; Y. Kawai, I. Yano, and K. Kaneda, Eur. J. Biochem. 171:73-80, 1988; Y. Kawai, I. Yano, K. Kaneda, and E. Yabuuchi, Eur. J. Biochem. 175:633-641, 1988). The 3-acyloxyacylamide structure is present in both the lipoamino acids and lipid A of lipopolysaccharide (endotoxin). The efficacy of lipoamino acids (an ornithine-containing lipid and a serine-containing lipid) in activating C3H/HeSlc mouse peritoneal exudate macrophages was compared with that of bacterial lipopolysaccharide, because the two types of substances were expected to exhibit similar biological activities and physiological functions on the basis of their structural similarities. Actually, the lipoamino acids, as well as lipopolysaccharide, strongly activated the macrophages to generate the immunoregulatory substances prostaglandin E2 and interleukin-1, but their effect on the induction of L929 cell cytolytic factor (a possible tumor necrosis factor), another immunoregulatory substance, was weaker than that of lipopolysaccharide. The effect of lipoamino acids on the cytotoxicity of macrophages for EL-4 leukemia cells was very weak. However, all of these activities, as far as tested, were strongly enhanced by synergistic action with gamma interferon. Only the serine-containing lipid killed both C3H/HeSlc and C3H/HeJ macrophages to almost the same degree as endotoxin killed C3H/HeSlc macrophages. On the other hand, lethal toxicity for mice was not found with either the ornithine-containing lipid or the serine-containing lipid, even when 7 mg of compound was injected into a mouse. These studies suggest that the lipoamino acids are nontoxic characteristic immunoactivators.
α-N-(3-酰氧基酰基)-鸟氨酸(或丝氨酸)是我们之前从一些革兰氏阴性菌中获得的脂氨基酸的结构(Y. Kawai和I. Yano,《欧洲生物化学杂志》136:531 - 538,1983;Y. Kawai、I. Yano和K. Kaneda,《欧洲生物化学杂志》171:73 - 80,1988;Y. Kawai、I. Yano、K. Kaneda和E. Yabuuchi,《欧洲生物化学杂志》175:633 - 641,1988)。3-酰氧基酰胺结构存在于脂氨基酸和脂多糖(内毒素)的脂质A中。比较了脂氨基酸(一种含鸟氨酸的脂质和一种含丝氨酸的脂质)与细菌脂多糖激活C3H/HeSlc小鼠腹腔渗出巨噬细胞的效果,因为基于它们的结构相似性,预计这两种物质会表现出相似的生物活性和生理功能。实际上,脂氨基酸以及脂多糖都能强烈激活巨噬细胞产生免疫调节物质前列腺素E2和白细胞介素-1,但它们对另一种免疫调节物质L929细胞溶细胞因子(一种可能的肿瘤坏死因子)诱导的作用比脂多糖弱。脂氨基酸对巨噬细胞对EL-4白血病细胞的细胞毒性作用非常弱。然而,就测试的所有这些活性而言,与γ干扰素的协同作用能使其显著增强。只有含丝氨酸的脂质对C3H/HeSlc和C3H/HeJ巨噬细胞的杀伤程度几乎与内毒素对C3H/HeSlc巨噬细胞的杀伤程度相同。另一方面,即使向小鼠注射7毫克化合物,含鸟氨酸的脂质或含丝氨酸的脂质对小鼠都未发现致死毒性。这些研究表明脂氨基酸是无毒的特征性免疫激活剂。