Endo N, Okuda T, Osada Y, Zen-yoji H
Department of Microbiology and Immunology, School of Health Sciences, Kyorin University, Tokyo, Japan.
Arzneimittelforschung. 1990 Jan;40(1):58-61.
Augmentative effects of muroctasin (N2-[(N-acetylmuramoyl)-L-alanyl-D-isoglutaminyl]-N6-stearoyl-L-lysine, (MDP-Lys(L18] on the production of a subcomponent of the first complement component, C1q, in mice were examined. The serum level of C1q in mice treated subcutaneously with muroctasin was found to be elevated significantly at 24 h (p less than 0.1) and 48 h (p less than 0.01). At 24 h, samples of peritoneal macrophages were derived from mice, and incubated with Dulbecco's Modified Eagle Medium (MEM) at 37 degrees C for 24 h. At 19 h of incubation, the C1q concentration in the supernatant of the culture also increased significantly (p less than 0.05). Moreover, when the peritoneal macrophages from non-treated mice were cultured in MEM containing muroctasin (0.001 microgram/ml), the amount of C1q in the culture supernatants also increased significantly 3 h (p less than 0.01) after cultivation. These results indicate that muroctasin activated C1q generation by macrophages in mice through direct and/or indirect mechanisms.
研究了胞壁酰三肽(N2-[(N-乙酰胞壁酰)-L-丙氨酰-D-异谷氨酰胺基]-N6-硬脂酰-L-赖氨酸,即MDP-Lys(L18))对小鼠体内第一补体成分C1q的一个亚成分产生的增强作用。皮下注射胞壁酰三肽的小鼠血清C1q水平在24小时(p<0.1)和48小时(p<0.01)时显著升高。在24小时时,从小鼠获取腹腔巨噬细胞样本,并在37℃下用杜尔贝科改良伊格尔培养基(MEM)孵育24小时。在孵育19小时时,培养上清液中的C1q浓度也显著增加(p<0.05)。此外,当将未处理小鼠的腹腔巨噬细胞在含有胞壁酰三肽(0.001微克/毫升)的MEM中培养时,培养3小时后(p<0.01),培养上清液中的C1q量也显著增加。这些结果表明,胞壁酰三肽通过直接和/或间接机制激活了小鼠巨噬细胞产生C1q。