Division of Reproduction, Department of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Anim Reprod Sci. 2010 Jun;119(3-4):244-57. doi: 10.1016/j.anireprosci.2010.01.005. Epub 2010 Jan 18.
Effects of semen components [fresh semen in extender, spermatozoa in extender (Spz), seminal plasma (SP)], or extender alone (Beltsville thawing solution, BTS) on the expression of selected cytokines [interleukin (IL)-1beta, IL-6, IL-10 and transforming growth factor (TGF)-beta1)] as well as the presence of cells positive for CD8 or CD25 were studied in the pig oviduct. In addition, cytokines in SP and oviductal flushings were analyzed. In experiment (Exp) I, groups of gilts were sampled at 5-6h after insemination with SP, Spz, fresh semen in BTS or only BTS (control). In Exp II, gilts were sampled 35-40 h after insemination with SP, Spz, BTS or only catheter insertion (control). Most oviductal flushing samples were positive (> or =detectable limits) for IL-10 and TGF-beta1 but only few for IL-6. The IHC-labelling of IL-6, IL-10 and TGF-beta1 was evident, especially in the epithelial cells of the isthmus and infundibulum as well as in the cells of the regional (mesometrial) lymph node. Cilia of the epithelium were positive for IL-6 (strongest in the infundibulum) and TGF-beta1 (strongest in the isthmus) but negative for IL-10. There were no consistent differences in IHC-labelling of the cytokines in relation to different treatments, except at 35-40 h after insemination (Exp II), when IL-6 was slightly higher in epithelium of the SP group and IL-10 in the infundibular connective tissue was higher in the SP and Spz groups. In the isthmus and infundibulum, there were no differences between animals inseminated with BTS (control) and the semen components for any of the cytokine mRNAs at 5-6h after insemination (Exp I). However, later (35-40 h, Exp II), insemination with SP, Spz and BTS alone appeared to up-regulate TGF-beta1 mRNA expression compared with the control group (without any fluid infused). In all treatment groups, the mRNA level for TGF-beta1 was higher than for IL-1beta, IL-6 and IL-10. Higher mRNA levels of all cytokines were found in the isthmus compared with the infundibulum. Numbers of CD8-positive cells (both in epithelium and connective tissue) appeared higher in the infundibulum compared with the isthmus and were mostly higher shortly (Exp I) after treatment with SP, SPZ and BTS than later (Exp II) in both segments. CD25-positive cells were few and found solely in the sub-epithelial connective tissue. The results indicate that in the porcine oviduct, IL-6, IL-10 and TGF-beta1 are endogenous produced and that TGF-beta1 may have a more important role for immunomodulation than the other cytokines, especially in isthmus. Differences between isthmus and infundibulum in cytokine mRNA expression and in presence of CD8-positive cells indicate different patterns of immune reactivity in the upper and lower parts of the oviduct.
本研究旨在探讨精液成分(新鲜精液中的精子、精子在稀释液中的状态(Spz)和精浆(SP))或单独的稀释液(Beltsville 解冻液,BTS)对猪输卵管中某些细胞因子(白细胞介素(IL)-1β、IL-6、IL-10 和转化生长因子(TGF)-β1)表达的影响,以及 CD8 或 CD25 阳性细胞的存在情况。此外,还分析了 SP 和输卵管冲洗液中的细胞因子。在实验 I 中,在输精后 5-6 小时,对不同处理组的母猪进行采样,处理组分别为 SP、Spz、新鲜精液+BTS 和仅用 BTS(对照组)。在实验 II 中,在输精后 35-40 小时,对 SP、Spz、BTS 或仅插入导管(对照组)的母猪进行采样。大多数输卵管冲洗样本中可检测到(>或=检测限)IL-10 和 TGF-β1,但仅少数样本中可检测到 IL-6。IL-6、IL-10 和 TGF-β1 的免疫组织化学标记物明显,尤其是在输卵管峡部和壶腹部的上皮细胞以及区域(系膜)淋巴结的细胞中。上皮细胞的纤毛对 IL-6(在壶腹部最强)和 TGF-β1(在峡部最强)呈阳性反应,但对 IL-10 呈阴性反应。除了输精后 35-40 小时(实验 II)外,不同处理组的细胞因子免疫组织化学标记物之间没有一致的差异,此时 SP 组上皮细胞中 IL-6 略高,SP 和 Spz 组壶腹部结缔组织中 IL-10 较高。在峡部和壶腹部,在输精后 5-6 小时(实验 I),与对照组(未注入任何液体)相比,用 BTS(对照组)和精液成分处理的母猪中,任何细胞因子的 mRNA 均无差异。然而,之后(35-40 小时,实验 II),与对照组相比,单独使用 SP、Spz 和 BTS 似乎会上调 TGF-β1 mRNA 的表达。在所有处理组中,TGF-β1 的 mRNA 水平均高于 IL-1β、IL-6 和 IL-10。与壶腹部相比,在峡部中发现所有细胞因子的 mRNA 水平均较高。与壶腹部相比,CD8 阳性细胞(上皮细胞和结缔组织中均有)在壶腹部中似乎更多,并且在 SP、SPZ 和 BTS 处理后不久(实验 I),尤其是在两个部位的后期(实验 II),都比之后更高。CD25 阳性细胞较少,仅存在于上皮下结缔组织中。结果表明,在猪输卵管中,IL-6、IL-10 和 TGF-β1 是内源性产生的,TGF-β1 可能比其他细胞因子在免疫调节中具有更重要的作用,尤其是在峡部。在输卵管峡部和壶腹部中,细胞因子 mRNA 表达和 CD8 阳性细胞的存在存在差异,表明输卵管上下部分的免疫反应模式不同。