白细胞介素5缺陷小鼠子宫嗜酸性粒细胞与生殖性能的关系。

S A Robertson, V J Mau, I G Young, K I Matthaei
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引用次数: 70

摘要

白细胞介素5在2型T淋巴细胞中表达,在驱动嗜酸性粒细胞的分化、募集和激活中起关键作用。白细胞介素5基因零突变的小鼠(IL-5 -/-小鼠)改变了2型免疫反应和严重减少的嗜酸性粒细胞群体。本研究探讨了白细胞介素5缺乏对雌性生殖道中大量嗜酸性粒细胞的影响,并测量了C57Bl/6 IL-5 -/-小鼠的生殖性能。根据其内源性过氧化物酶活性检测,IL-5 -/-小鼠的子宫内膜嗜酸性粒细胞在发情周期和妊娠早期数量减少了4 - 7倍。分娩时子宫颈和个体组织中的嗜酸性粒细胞也同样减少。在这些组织中,嗜酸性粒细胞募集和定位的时间波动没有变化,表明白细胞介素5不是女性生殖道中必要的趋化剂。由于发情期较长(IL-5 -/-小鼠每周期2.7 +/- 0.9天,而IL-5 +/-小鼠每周期1.8 +/- 0.7天),IL-5 -/-小鼠的发情周期较长(IL-5 -/-小鼠平均+/- SD = 5.6 +/- 1.0天,IL-5 +/-小鼠平均+/- SD = 5.0 +/- 0.8天)。在白细胞介素5缺乏的小鼠中,雌性与雄性交配的间隔时间和发现交配栓的间隔时间明显缩短。无论妊娠是由同基因(C57Bl/6)还是同种异体(CBA或Balb/c)雄性小鼠产生的,IL-5 -/-和IL-5 +/+小鼠的着床率和随后的胎儿发育是相似的,除了CBA雄性小鼠在第17天的胎盘大小增加10%,胎盘与胎儿比例减少6.5%。白细胞介素5缺陷小鼠的分娩和产后子宫修复没有受到损害,这是通过妊娠时间长短和产后发情时开始的妊娠结果来判断的。幼崽的出生体重和生长轨迹受到白细胞介素5状态的显著影响,IL-5 -/-幼崽,特别是C57Bl/6和CBA F(1)幼崽的体重轻微但显著增加,这种增加一直持续到成年。这些数据与嗜酸性粒细胞在与发情周期相关的子宫内膜组织重塑中起作用的观点一致,但表明在母体和胎儿缺乏白细胞介素5的情况下,妊娠和分娩的事件进行得相当正常。然而,白细胞介素5缺乏对胎盘生长和功能以及新生儿体重增加的品系依赖性影响表明,这种细胞因子可能通过母体或胎儿免疫轴起作用,对生殖结果产生微妙的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uterine eosinophils and reproductive performance in interleukin 5-deficient mice.

Interleukin 5 is expressed in type 2 T lymphocytes and has a key role in driving the differentiation, recruitment and activation of eosinophils. Mice with a null mutation in the interleukin 5 gene (IL-5 -/- mice) have altered type 2 immune responses and severely depleted eosinophil populations. In the present study, the effect of interleukin 5 deficiency on the abundant population of eosinophils present in the female reproductive tract was investigated, and the reproductive performance in C57Bl/6 IL-5 -/- mice was measured. Endometrial eosinophils, detected on the basis of their endogenous peroxidase activity, were reduced in number by four-sevenfold during the oestrous cycle and in early pregnancy in IL-5 -/- mice. Eosinophils present in the cervix and decidual tissues at the time of parturition were similarly diminished. The temporal fluctuations in eosinophil recruitment and localization within these tissues were otherwise unchanged, indicating that interleukin 5 is not a necessary chemotactic agent in the female reproductive tract. Oestrous cycles were moderately greater in duration in IL-5 -/- mice (mean +/- SD = 5.6 +/- 1.0 days in IL-5 -/- mice versus 5.0 +/- 0.8 days in IL-5 +/+ mice), owing to an extended period in oestrus (2.7 +/- 0.9 days per cycle in IL-5 -/- mice versus 1.8 +/- 0.7 in IL-5 +/+ mice). The interval between placing females with males and the finding of copulatory plugs was reduced significantly in interleukin 5-deficient mice. Implantation rates and subsequent fetal development were comparable in IL-5 -/- and IL-5 +/+ mice, irrespective of whether pregnancies were sired by syngeneic (C57Bl/6) or allogeneic (CBA or Balb/c) males, apart from a 10% increase in placental size and a 6.5% decrease in placental∶fetal ratio seen on day 17 in pregnancies sired by CBA males. Parturition and post-partum uterine repair were not compromised in interleukin 5-deficient mice, as judged by the length of gestation, and the outcomes of pregnancies initiated at post-partum oestrus. The birth weights and growth trajectories of pups were significantly influenced by interleukin 5 status, with small but significant increases in the weights of IL-5 -/- pups, particularly C57Bl/6 and CBA F(1) animals, remaining evident until adulthood. These data are consistent with the view that eosinophils have a role in endometrial tissue remodelling associated with the oestrous cycle, but indicate that the events of pregnancy and parturition proceed quite normally in the absence of maternal and fetal interleukin 5. However, strain-dependent effects of interleukin 5 deficiency on placental growth and function and subsequent weight gain in the newborn indicate that this cytokine may act through the maternal or fetal immune axis to exert subtle influences on reproductive outcome.

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