Witkin S S
Clin Exp Immunol. 1986 May;64(2):364-9.
The ability of seminal fluid (SF) to induce suppressor cell activity from peripheral blood mononuclear cells (PBMN) was examined. PBMN were incubated with SF for 48 h, washed to remove SF components, treated with mitomycin C (mit C) and co-cultured with Raji cells, a lymphoblastoid cell line. Raji cell proliferation was inhibited by SF-treated PBMN proportionally to SF concentration. SF (50-200 micrograms), mit C-treated Raji cells or mit C-treated PBMN pre-incubated with phytohaemagglutinin were without effect on Raji cell growth. Suppressor T lymphocytes generated by incubation of PBMN with concanavalin A inhibited Raji cells to the same extent as did SF-treated PBMN. All activity was lost following heating at 56 degrees C for 30 min; freezing and thawing reduced the ability of SF to induce suppression by 50%. Dialysis of SF or treatment with antibody to prostaglandin E2 led to a 50% reduction in suppression.
研究了精液(SF)诱导外周血单个核细胞(PBMN)产生抑制细胞活性的能力。将PBMN与SF孵育48小时,洗涤以去除SF成分,用丝裂霉素C(mit C)处理,并与淋巴母细胞系Raji细胞共培养。经SF处理的PBMN对Raji细胞增殖的抑制作用与SF浓度成比例。SF(50 - 200微克)、经mit C处理的Raji细胞或预先用植物血凝素孵育的经mit C处理的PBMN对Raji细胞生长无影响。通过将PBMN与伴刀豆球蛋白A孵育产生的抑制性T淋巴细胞对Raji细胞的抑制程度与经SF处理的PBMN相同。在56℃加热30分钟后所有活性丧失;冻融使SF诱导抑制的能力降低50%。SF的透析或用前列腺素E2抗体处理导致抑制作用降低50%。