Ogata M, Matsui T, Kita T, Shigematsu A
Department of Anesthesiology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Infect Immun. 1999 Jul;67(7):3284-9. doi: 10.1128/IAI.67.7.3284-3289.1999.
We have previously reported that pretreatment with carrageenan (CAR) enhances lipopolysaccharide (LPS)-induced tumor necrosis factor alpha (TNF-alpha) production in and lethality for mice. Whole blood cultured in vitro was used to show that CAR pretreatment results in about a 200-fold increase in LPS-induced TNF-alpha production. CAR by itself did not induce TNF-alpha production. However, CAR-treated cultured medium sensitized whole blood to make more LPS-induced TNF than did saline-treated cultured medium in vitro. It was also demonstrated that CAR pretreatment increases TNF-alpha mRNA levels of both blood cells and peritoneal exudate cells, but not of bone marrow cells. Immunoelectron microscopic analysis revealed that polymorphonuclear leukocytes and macrophages are TNF-alpha-producing cells in CAR-treated mice. In CAR-treated mice, TNF-alpha was seen early after LPS injection in leukocytes in hepatic sinusoids and on the surfaces of endothelial cells. TNF-alpha was also detected late after LPS injection in hepatocytes which become edematous. These results suggest that CAR primes leukocytes to produce TNF-alpha in response to LPS and that they play an important role in the pathogenesis of liver injury.
我们之前报道过,用角叉菜胶(CAR)预处理可增强脂多糖(LPS)诱导的小鼠肿瘤坏死因子α(TNF-α)的产生及致死率。体外培养的全血实验表明,CAR预处理可使LPS诱导的TNF-α产生增加约200倍。CAR本身不会诱导TNF-α的产生。然而,经CAR处理的培养基使全血对LPS诱导产生更多TNF,比经生理盐水处理的培养基在体外的效果更好。还证实,CAR预处理可增加血细胞和腹腔渗出细胞中TNF-α的mRNA水平,但骨髓细胞中则不会增加。免疫电子显微镜分析显示,在经CAR处理的小鼠中,多形核白细胞和巨噬细胞是产生TNF-α的细胞。在经CAR处理的小鼠中,LPS注射后早期,在肝血窦中的白细胞和内皮细胞表面可见TNF-α。LPS注射后晚期,在出现水肿的肝细胞中也检测到TNF-α。这些结果表明,CAR使白细胞对LPS产生反应而产生TNF-α,且它们在肝损伤的发病机制中起重要作用。