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绵羊子宫乳蛋白对植物血凝素刺激的淋巴细胞增殖的抑制作用。

Suppression of phytohemagglutinin-stimulated lymphocyte blastogenesis by ovine uterine milk protein.

作者信息

Segerson E C, Moffatt R J, Bazer F W, Roberts R M

出版信息

Biol Reprod. 1984 Jun;30(5):1175-86. doi: 10.1095/biolreprod30.5.1175.

Abstract

Two basic glycoproteins (UTM-P) with molecular weights of 57,000 and 59,000 were purified from ovine uterine milk collected on Days 125 and 130 of pregnancy. The UTM-P were evaluated for immunosuppressive activity in phytohemagglutinin (PHA)-treated, mixed lymphocyte (MLC) and resting lymphocyte (RLC) cultures. For PHA and RLC cultures, UTM-P (2.5 to 800 micrograms UTM-P/ml) were added to 1 X 10(6) lymphocytes and 0.8 micrograms of PHA (for PHA cultures only), while for the MLC, UTM-P (50 to 1600 micrograms UTM-P/ml) were added to 5 X 10(5) lymphocytes combined from each of two ewes. Following [3H] thymidine addition, cells were later harvested for determination of thymidine incorporation. Lymphocyte blastogenesis was suppressed by UTM-P in PHA (R2 = 0.32 to 0.92, P less than 0.01 to 0.001), MLC (R2 = 0.8, P less than 0.001) and RLC (R2 = 0.65, P les than 0.01) experiments. To determine reversibility, PHA-treated lymphocytes were incubated with UTM-P for 6, 12 or 24 h, then washed to remove surface UTM-P. Incubation was continued in the presence of PHA as with other experiments. Exposure of lymphocytes to UTM-P for 6 or 12 h did not result in suppression of blastogenesis, whereas exposure for 24 h was sufficient for suppression (P less than 0.01). In an additional experiment, UTM-P were added to PHA-treated cultures at 0, 6, 12 or 24 h. Suppression (P less than 0.01) of blastogenesis was observed for each time period. Immunosuppressive activity was not mediated by overall cytotoxicity and was not affected by routine handling and storage of UTM-P. Data from these experiments provide one explanation for tolerance of the conceptus allograft during defined stages of ovine pregnancy.

摘要

从怀孕125天和130天收集的绵羊子宫乳中纯化出两种分子量分别为57,000和59,000的基本糖蛋白(UTM-P)。对UTM-P在植物血凝素(PHA)处理的混合淋巴细胞(MLC)和静息淋巴细胞(RLC)培养物中的免疫抑制活性进行了评估。对于PHA和RLC培养物,将UTM-P(2.5至800微克UTM-P/毫升)加入到1×10⁶个淋巴细胞和0.8微克PHA(仅用于PHA培养物)中,而对于MLC,将UTM-P(50至1600微克UTM-P/毫升)加入到来自两只母羊的5×10⁵个淋巴细胞中。加入[³H]胸腺嘧啶核苷后,随后收获细胞以测定胸腺嘧啶核苷掺入量。在PHA(R² = 0.32至0.92,P<0.01至0.001)、MLC(R² = 0.8,P<0.001)和RLC(R² = 0.65,P<0.01)实验中,UTM-P抑制了淋巴细胞增殖。为了确定可逆性,将PHA处理的淋巴细胞与UTM-P孵育6、12或24小时,然后洗涤以去除表面的UTM-P。与其他实验一样,在PHA存在下继续孵育。淋巴细胞暴露于UTM-P 6或12小时未导致增殖抑制,而暴露24小时足以产生抑制作用(P<0.01)。在另一项实验中,在0、6、12或24小时将UTM-P加入到PHA处理的培养物中。在每个时间段均观察到增殖抑制(P<0.01)。免疫抑制活性不是由总体细胞毒性介导的,并且不受UTM-P常规处理和储存的影响。这些实验的数据为绵羊妊娠特定阶段同种异体胚胎的耐受性提供了一种解释。

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