Yokochi T, Inoue Y, Yokoo J, Kimura Y, Kato N
Department of Microbiology, Fukui Medical School, Japan.
Infect Immun. 1989 Jun;57(6):1786-91. doi: 10.1128/iai.57.6.1786-1791.1989.
The tissue distribution of Klebsiella pneumoniae O3 lipopolysaccharide (KO3 LPS) was studied in mice injected subcutaneously (s.c.) or intraperitoneally (i.p.) with 125I-labeled KO3 LPS. Marked retention of KO3 LPS radioactivity could be found at the site of s.c. injection for several weeks. On the other hand, about 85% of the radioactivity rapidly disappeared from the peritoneal cavity within 6 h after i.p. injection. The long-term presence of KO3 LPS at the injection site was also supported by experiments with 51Cr-labeled KO3 LPS and immunoblotting and immunofluorescence staining methods. The R-form LPS lacking the O-specific polysaccharide chain of KO3 LPS and the lipid A fraction of KO3 LPS seemed to remain at the site in larger amounts and for longer times than KO3 LPS. There were no marked differences in the retention pattern at the injection site among KO3 LPS, Escherichia coli LPS, Salmonella typhosa LPS, and Salmonella enteritidis LPS. However, much less radioactivity accumulated in the livers and spleens of mice injected with either KO3 LPS or S. typhosa LPS compared with the other LPS preparations. It was suggested that retention of LPS at the site of s.c. injection may play an important role in the development of various biological actions of s.c. injected LPS.
用125I标记的肺炎克雷伯菌O3脂多糖(KO3 LPS)对小鼠进行皮下(s.c.)或腹腔内(i.p.)注射,研究了KO3 LPS的组织分布。皮下注射部位可发现KO3 LPS放射性明显保留数周。另一方面,腹腔注射后6小时内,约85%的放射性迅速从腹腔消失。用51Cr标记的KO3 LPS以及免疫印迹和免疫荧光染色方法进行的实验也支持了KO3 LPS在注射部位的长期存在。缺乏KO3 LPS O特异性多糖链的R型LPS和KO3 LPS的脂质A部分似乎比KO3 LPS在该部位停留的量更大、时间更长。KO3 LPS、大肠杆菌LPS、伤寒沙门氏菌LPS和肠炎沙门氏菌LPS在注射部位的保留模式没有明显差异。然而,与其他LPS制剂相比,注射KO3 LPS或伤寒沙门氏菌LPS的小鼠肝脏和脾脏中积累的放射性要少得多。有人认为,皮下注射LPS在皮下注射部位的保留可能在皮下注射LPS的各种生物学作用的发展中起重要作用。