Kirikae T, Hirata M, Yamasu H, Kirikae F, Tamura H, Kayama F, Nakatsuka K, Yokochi T, Nakano M
Department of Microbiology, Jichi Medical School, Tochigi-ken, Japan.
Infect Immun. 1998 May;66(5):1861-8. doi: 10.1128/IAI.66.5.1861-1868.1998.
CAP18 (an 18-kDa cationic antimicrobial protein) is a granulocyte-derived protein that can bind lipopolysaccharide (LPS) and inhibit various activities of LPS in vitro. The present study examined the protective effect of a synthetic 27-amino-acid peptide (CAP18(109-135)) from the LPS-binding domain of CAP18 against antibiotic-induced endotoxin shock, using highly LPS-sensitive D-(+)-galactosamine (D-GalN)-sensitized C3H/HeN mice. The antibiotic-induced endotoxin (CAZ-endotoxin) was prepared from the culture filtrate of Pseudomonas aeruginosa PAO1 exposed to ceftazidime (CAZ). Injection of CAP18(109-135) protected the mice injected with LPS or CAZ-endotoxin from death and lowered their tumor necrosis factor (TNF) levels in serum in a dose-dependent manner. Treatment with CAZ caused death of the D-GalN-sensitized P. aeruginosa PAO-infected mice within 48 h, while injection with CAP18(109-135) rescued the mice from death. In the mice rescued from death by injection with CAP18(109-135), endotoxin levels in plasma and TNF production by liver tissues were decreased but the numbers of viable infecting bacteria in their blood were not decreased significantly and remained at the levels in CAZ-treated mice. These results indicate that CAP18(109-135) is capable of preventing antibiotic-induced endotoxic shock in mice with septicemia and that the effect is due to its LPS-neutralizing activity rather than to its antibacterial activity.
CAP18(一种18 kDa的阳离子抗菌蛋白)是一种源自粒细胞的蛋白质,它能够结合脂多糖(LPS)并在体外抑制LPS的多种活性。本研究使用对LPS高度敏感的D-(+)-半乳糖胺(D-GalN)致敏的C3H/HeN小鼠,检测了来自CAP18的LPS结合结构域的一种合成27氨基酸肽(CAP18(109 - 135))对抗生素诱导的内毒素休克的保护作用。抗生素诱导的内毒素(CAZ-内毒素)是由暴露于头孢他啶(CAZ)的铜绿假单胞菌PAO1的培养滤液制备而成。注射CAP18(109 - 135)可保护注射LPS或CAZ-内毒素的小鼠免于死亡,并以剂量依赖的方式降低其血清中的肿瘤坏死因子(TNF)水平。用CAZ治疗会导致D-GalN致敏的铜绿假单胞菌PAO感染的小鼠在48小时内死亡,而注射CAP18(109 - 135)可使小鼠免于死亡。在通过注射CAP18(109 - 135)而获救的小鼠中,血浆中的内毒素水平和肝脏组织产生的TNF减少,但它们血液中存活的感染细菌数量没有显著减少,仍保持在CAZ治疗小鼠的水平。这些结果表明,CAP18(109 - 135)能够预防败血症小鼠中抗生素诱导的内毒素休克,且该作用归因于其LPS中和活性而非抗菌活性。