Hamada S, McGhee J R, Kiyono H, Torii M, Michalek S M
J Immunol. 1981 Jun;126(6):2279-83.
The mitogenic activity of various purified serotype carbohydrate and cell wall lysate fractions of Streptococcus mutans for murine lymphocytes has been determined. The highest mitogenic responses occurred after 48 hr of stimulation with these carbohydrate preparations when tested on splenic cultures derived from C3H/HeJ and BALB/c mice. The response pattern obtained with optimum concentrations of these preparations was very similar to that seen with the B cell mitogen, LPS. A purified serotype g carbohydrate (M1 g) prepared by mutanolysin enzyme treatment of S. mutans 6715 cell walls stimulated good mitogenic responses in BALB/c nude and nu/+ splenic cultures, suggesting an effect on mouse B cells. This was further substantiated by studies showing that this antigen also induced responses in cultures of B cells purified by nylon wool fractionation, whereas purified T cells did not respond. Mitogenic responses were due to the carbohydrate moiety and not to possible LPS contamination, since alkaline treatment or mixture with polymyxin B greatly reduced responses to LPS; however, no alteration of mitogenic responses to M1 g occurred. Further, LPS nonresponsive C3H/HeJ spleen cells yielded good mitogenic responses to M1 g. On the other hand, periodate treatment, which is known to decompose carbohydrate moieties completely abrogated the mitogenic activity of M1 g antigen. Additional studies with serotypes c and e carbohydrate, which also induced mitogenic responses, suggested that this activity for lymphoid cells may be a common property of S. mutans cell wall carbohydrate.
已测定变形链球菌各种纯化血清型碳水化合物和细胞壁裂解物组分对小鼠淋巴细胞的促有丝分裂活性。在用这些碳水化合物制剂刺激48小时后,对来自C3H/HeJ和BALB/c小鼠的脾细胞培养物进行测试时,观察到最高的促有丝分裂反应。这些制剂的最佳浓度所获得的反应模式与B细胞促有丝分裂原LPS所观察到的模式非常相似。通过变溶菌素酶处理变形链球菌6715细胞壁制备的纯化血清型g碳水化合物(M1g)在BALB/c裸鼠和nu/+脾细胞培养物中刺激出良好的促有丝分裂反应,表明对小鼠B细胞有作用。通过研究进一步证实了这一点,研究表明该抗原在通过尼龙毛分级分离纯化的B细胞培养物中也诱导反应,而纯化的T细胞则无反应。促有丝分裂反应是由于碳水化合物部分,而不是可能的LPS污染,因为碱性处理或与多粘菌素B混合大大降低了对LPS的反应;然而,对M1g的促有丝分裂反应没有改变。此外,对LPS无反应的C3H/HeJ脾细胞对M1g产生良好的促有丝分裂反应。另一方面,已知能完全分解碳水化合物部分的高碘酸盐处理完全消除了M1g抗原的促有丝分裂活性。对也诱导促有丝分裂反应的血清型c和e碳水化合物的进一步研究表明,这种对淋巴细胞的活性可能是变形链球菌细胞壁碳水化合物的共同特性。