Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Canada.
J Cell Mol Med. 2013 Jan;17(1):90-102. doi: 10.1111/j.1582-4934.2012.01650.x. Epub 2012 Dec 4.
This study aimed to determine the mechanism of uterine activation during labour, both term (TL) and preterm (PTL). We hypothesized that the peripheral leucocytes are recruited to uterine tissues by locally produced cytokines where they contribute to the initiation of parturition. Mouse uteri were collected (i) during gestation, TL and post-partum (PP), (ii) during PTL initiated by intrauterine infusion of LPS (125 μg) or (iii) injection of the progesterone receptor antagonist RU486 and analysed for multiple cytokine expression levels by real-time polymerase chain reaction (RT-PCR) and 23-plex Cytokine assay or enzymatically dispersed for assessment of immune cell populations. Markers of myeloid cell differentiation (Gr1, Neu7/4 and F4/80) were evaluated by FACS to define tissue macrophages (Macs), monocytes (M) and neutrophils (N) and by immunohistochemistry to detect tissue Macs and N. Our results indicate that: (1) Macs were elevated in mouse myometrium before TL (P < 0.05) followed by an increase in M and N; these changes were accompanied by an increase in multiple pro-inflammatory cytokines/chemokines genes. The expression of corresponding proteins increased PP. (2) TL and RU486-PTL models showed similar gene/protein expression profiles, (3) LPS-PTL was characterized by strong pro-inflammatory response and massive influx of N in myometrial tissues showing a pattern different from TL and RU486-PTL, (4) The PP period appears similar in all three models, with elevated myometrial cytokine levels and high infiltration of immune cells. We concluded that leucocytes infiltrate myometrium around the time of parturition implicating their potential role in labour activation (both term and preterm) and major role in PP uterine involution.
本研究旨在确定分娩过程中足月(TL)和早产(PTL)子宫激活的机制。我们假设外周白细胞通过局部产生的细胞因子募集到子宫组织中,从而有助于分娩的开始。收集小鼠子宫(i)在妊娠、TL 和产后(PP)期间,(ii)在宫内注射 LPS(125μg)或(iii)注射孕激素受体拮抗剂 RU486 引发 PTL 期间,并通过实时聚合酶链反应(RT-PCR)和 23 倍细胞因子分析检测多种细胞因子表达水平或通过酶法分散评估免疫细胞群。通过流式细胞术评估髓样细胞分化标志物(Gr1、Neu7/4 和 F4/80),以定义组织巨噬细胞(Macs)、单核细胞(M)和中性粒细胞(N),并通过免疫组织化学检测组织 Macs 和 N。我们的结果表明:(1)在 TL 之前,小鼠子宫肌层中的 Macs 升高(P<0.05),随后 M 和 N 增加;这些变化伴随着多种促炎细胞因子/趋化因子基因的增加。相应蛋白的表达在 PP 时增加。(2)TL 和 RU486-PTL 模型显示出相似的基因/蛋白表达谱,(3)LPS-PTL 表现出强烈的促炎反应和大量中性粒细胞涌入子宫肌层,表现出与 TL 和 RU486-PTL 不同的模式,(4)在所有三种模型中,PP 期似乎相似,具有升高的子宫肌层细胞因子水平和大量免疫细胞浸润。我们得出结论,白细胞浸润到分娩时的子宫肌层,暗示它们在分娩激活(足月和早产)中的潜在作用以及在 PP 子宫复旧中的主要作用。