Kelly N M, Young L, Cross A S
Department of Bacterial Diseases, Walter Reed Army Institute of Research, Washington, D.C. 20307-5100.
Infect Immun. 1991 Dec;59(12):4491-6. doi: 10.1128/iai.59.12.4491-4496.1991.
The lipid A portion of the lipopolysaccharide (LPS) molecule of gram-negative bacteria has the ability to turn on the production of tumor necrosis factor (TNF) in macrophage cells. The question addressed in this paper was whether the presence of the polysaccharide moiety on the LPS molecule had any bearing on this ability. The question was asked (i) by using isolated LPS from a series of Salmonella mutants having progressively less polysaccharide attached to the lipid A portion of the molecule and (ii) by using whole bacteria expressing alternatively the smooth or rough LPS phenotype. Isolated LPS and bacteria were examined for their abilities to induce bioactive TNF in the mouse macrophage cell line RAW 264.7. The results indicated that the presence of long- or short-chain polysaccharide moieties had no bearing on the ability of the isolated LPS molecule to induce TNF. However, the presence of long-chain polysaccharides attached to the lipid moiety on the intact smooth bacterium was associated with a decreased ability to induce TNF. To test whether the bacteria were inducing TNF by a cell (bacterium)-to-cell (macrophage) contact mechanism or through a releasable product, the bacteria were removed from direct contact with the macrophage cells by using a Transwell filter insert. Under these conditions the rough bacteria continued to induce TNF, while the smooth bacteria were no longer capable of doing so. When filtrates from the bacteria were examined in the Limulus amebocyte lysate assay, the results showed that the rough bacteria were releasing approximately a log order more Limulus amebocyte lysate activity than the smooth bacteria. The results of this study suggest that rough bacteria may be superior inducers of TNF compared with their smooth counterparts because of a greater propensity to shed their LPS.
革兰氏阴性菌脂多糖(LPS)分子的脂质A部分能够开启巨噬细胞中肿瘤坏死因子(TNF)的产生。本文探讨的问题是LPS分子上多糖部分的存在是否与这种能力有关。该问题通过以下方式进行研究:(i)使用从一系列沙门氏菌突变体中分离出的LPS,这些突变体分子脂质A部分连接的多糖逐渐减少;(ii)使用交替表达光滑型或粗糙型LPS表型的完整细菌。检测分离出的LPS和细菌在小鼠巨噬细胞系RAW 264.7中诱导生物活性TNF的能力。结果表明,长链或短链多糖部分的存在与分离出的LPS分子诱导TNF的能力无关。然而,完整光滑型细菌脂质部分连接的长链多糖的存在与诱导TNF的能力降低有关。为了测试细菌是通过细胞(细菌)与细胞(巨噬细胞)接触机制还是通过可释放产物诱导TNF,使用Transwell滤膜插入物使细菌与巨噬细胞不直接接触。在这些条件下,粗糙型细菌继续诱导TNF,而光滑型细菌则不再能够诱导。当在鲎试剂检测中检测细菌滤液时,结果表明粗糙型细菌释放的鲎试剂活性比光滑型细菌大约高一个对数级。本研究结果表明,与光滑型细菌相比,粗糙型细菌可能是TNF的更高效诱导剂,因为它们更倾向于释放其LPS。