Okumura S, Nitta T, Nakano M
Microbiol Immunol. 1981;25(11):1139-49. doi: 10.1111/j.1348-0421.1981.tb00122.x.
Mitogenicity and the polyclonal plaque forming cell (PFC)-inducing property of a water soluble-adjuvant extracted from Bacterionema matruchotii by butanol (Bu-WSA) were examined in vitro in the spleen cells of hybrid (CBA/N female X BALB/c male)F1 mice and C3H strain of mice. The hybrid F1 male cells which expressed a CBA/N-defect were unable to respond to Bu-WSA, when assessed by the incorporation of [3H]thymidine into the cells and the generation of anti-trinitrophenyl (TNP)-PFC or autoantibody PFC defined by the anti-bromelain-treated mouse erythrocyte PFC assay. However, hybrid F1 female cells with normal traits responded to Bu-WSA. Cultured spleen cells of bacterial lipopolysaccharide (LPS)-nonresponsive (C3H/HeJ mice responded to Bu-WSA as in the case of cells of LPS-responsive C3H/He mice, and the [3H]thymidine-uptakes and the numbers of PFC in these culture cells increased. Re-extraction of Bu-WSA by phenol did not affect its activities, while the activity of butanol-extracted LPS and C3H/HeJ cells decreased after re-extraction by the same procedure with phenol.
用丁醇从龋齿杆菌中提取的水溶性佐剂(Bu-WSA)的促有丝分裂性和诱导多克隆空斑形成细胞(PFC)的特性,在体外对杂种(CBA/N雌性×BALB/c雄性)F1小鼠和C3H品系小鼠的脾细胞进行了检测。当通过将[3H]胸苷掺入细胞以及通过抗菠萝蛋白酶处理的小鼠红细胞PFC测定法确定的抗三硝基苯基(TNP)-PFC或自身抗体PFC的产生来评估时,表达CBA/N缺陷的杂种F1雄性细胞对Bu-WSA无反应。然而,具有正常特征的杂种F1雌性细胞对Bu-WSA有反应。细菌脂多糖(LPS)无反应性的C3H/HeJ小鼠的培养脾细胞对Bu-WSA的反应与LPS有反应性的C3H/He小鼠的细胞相同,并且这些培养细胞中的[3H]胸苷摄取量和PFC数量增加。用苯酚对Bu-WSA进行再提取不影响其活性,而用相同的苯酚提取程序对丁醇提取的LPS和C3H/HeJ细胞进行再提取后,其活性降低。