Nagao S, Akagawa K S, Okada F, Harada Y, Yagawa K, Kato K, Tanigawa Y
Department of Biochemistry, Shimane Medical University, Japan.
Microbiol Immunol. 1992;36(11):1155-71. doi: 10.1111/j.1348-0421.1992.tb02119.x.
The effect of various bacterial cell wall components on in vitro biological function of murine peritoneal exudate macrophages was evaluated. We examined four different parameters of metabolic activity and monokine secretion. Peritoneal exudate macrophages from rats and guinea pigs, all of the strains tested, were stimulated by whole bacterial cell wall preparations, purified bacterial cell wall peptidoglucans, its water-soluble peptidolglycan fragments, muramyl dipeptides and amphipathic substances. Murine peritoneal exudate macrophages were activated by amphipathic substances of gram-positive bacteria. However, macrophages from mice, irrespective of strains, were not stimulated in the in vitro assay systems by purified bacterial cell wall peptidoglycan, water-soluble bacterial peptidoglycan fragments or muramyl dipeptides. These results suggest that macrophage activation by bacterial peptidoglycan in vitro is animal species specific.
评估了各种细菌细胞壁成分对小鼠腹腔渗出巨噬细胞体外生物学功能的影响。我们检测了代谢活性和单核因子分泌的四个不同参数。来自大鼠和豚鼠的腹腔渗出巨噬细胞,在所有测试菌株中,均受到完整细菌细胞壁制剂、纯化的细菌细胞壁肽聚糖、其水溶性肽聚糖片段、胞壁酰二肽和两亲性物质的刺激。革兰氏阳性菌的两亲性物质激活了小鼠腹腔渗出巨噬细胞。然而,在体外测定系统中,来自小鼠的巨噬细胞,无论菌株如何,均未受到纯化的细菌细胞壁肽聚糖、水溶性细菌肽聚糖片段或胞壁酰二肽的刺激。这些结果表明,细菌肽聚糖在体外对巨噬细胞的激活具有动物物种特异性。