Wannemuehler M J, Michalek S M, Jirillo E, Williamson S I, Hirasawa M, McGhee J R
J Immunol. 1984 Jul;133(1):299-305.
Recent studies have suggested that lipopolysaccharide (LPS) derived from gram-negative organisms such as Bacteroides, which are not members of the Enterobacteriaceae, stimulate B cells from the classic LPS-hyporesponsive C3H/HeJ mouse. In the present study, purified, phenol-water-extracted LPS from Bacteroides fragilis ATCC 25285 (B-LPS) was tested for its ability to induce in vivo and in vitro responses in classic LPS-responsive C3H/HeN, LPS-hyporesponsive C3H/HeJ, and (C3H/HeN X C3H/HeJ)F1 hybrid mice. B-LPS induced mitogenic responses in both C3H/HeN and C3H/HeJ spleen cell cultures when cells were cultured under standard conditions, i.e., 8 X 10(5) cells/well. Interestingly, when lower spleen cell numbers were tested with B-LPS, a typical responsive-nonresponsive pattern developed in which good mitogenic responses were induced by B-LPS in C3H/HeN cultures and in which low responses in C3H/HeJ spleen cell cultures were evident. In vivo immunization of mice with B-LPS resulted in high antibody responses in C3H/HeN, intermediate responses in F1, and low responses in C3H/HeJ mice. When purified splenic B cells were incubated with B-LPS, both mitogenic responses and polyclonal immunoglobulin M (IgM) synthesis occurred in C3H/HeN cultures, whereas intermediate responses were noted in F1 cultures and no response was seen in B cell cultures from C3H/HeJ mice. Furthermore, in vitro TNP-B-LPS responses were induced in C3H/HeN spleen cells or purified B cell cultures, and intermediate anti-TNP PFC responses occurred in F1 spleen cells or purified B cell cultures. The toxicity of B-LPS was tested in galactosamine-sensitized mice. The LD50 values for B-LPS in classic LPS-responsive C3H/HeN and C57BL/6J mice were 0.6 microgram and 1.1 microgram, respectively; F1 hybrid mice were approximately 15-fold more resistant, whereas C3H/HeJ mice gave an LD50 of 1650 micrograms. This study shows that phenol-water preparations of B-LPS are biologically active and induce responses in the classic LPS-responsive but not in the LPS-hyporesponsive C3H/HeJ mouse strain.
最近的研究表明,来源于革兰氏阴性菌(如拟杆菌,它们不是肠杆菌科成员)的脂多糖(LPS)可刺激经典的LPS低反应性C3H/HeJ小鼠的B细胞。在本研究中,对从脆弱拟杆菌ATCC 25285中纯化的、经酚水提取的LPS(B-LPS)在经典LPS反应性C3H/HeN、LPS低反应性C3H/HeJ以及(C3H/HeN×C3H/HeJ)F1杂交小鼠体内和体外诱导反应的能力进行了测试。当细胞在标准条件下(即8×10⁵个细胞/孔)培养时,B-LPS在C3H/HeN和C3H/HeJ脾细胞培养物中均诱导出促有丝分裂反应。有趣的是,当用较低数量的脾细胞与B-LPS进行测试时,出现了一种典型的反应-无反应模式,即B-LPS在C3H/HeN培养物中诱导出良好的促有丝分裂反应,而在C3H/HeJ脾细胞培养物中反应较低。用B-LPS对小鼠进行体内免疫,在C3H/HeN小鼠中产生高抗体反应,在F1小鼠中产生中等反应,而在C3H/HeJ小鼠中产生低反应。当将纯化的脾B细胞与B-LPS一起孵育时,C3H/HeN培养物中出现促有丝分裂反应和多克隆免疫球蛋白M(IgM)合成,而在F1培养物中观察到中等反应,在C3H/HeJ小鼠的B细胞培养物中未观察到反应。此外,在C3H/HeN脾细胞或纯化的B细胞培养物中诱导出体外TNP-B-LPS反应,在F1脾细胞或纯化的B细胞培养物中出现中等的抗TNP PFC反应。在半乳糖胺致敏的小鼠中测试了B-LPS的毒性。B-LPS在经典LPS反应性C3H/HeN和C57BL/6J小鼠中的LD50值分别为0.6微克和1.1微克;F1杂交小鼠的抗性约高15倍,而C3H/HeJ小鼠的LD50为1650微克。本研究表明,B-LPS的酚水制剂具有生物活性,可在经典LPS反应性小鼠品系中诱导反应,但在LPS低反应性C3H/HeJ小鼠品系中则不然。