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首页> 外文期刊>Journal of cellular and molecular medicine. >Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice
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Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice

机译:子宫肌层免疫细胞有助于小鼠的足月分娩,早产和产后复旧

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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.
机译:本研究旨在确定分娩期(TL)和早产期(PTL)的分娩过程中子宫激活的机制。我们假设外周血白细胞被局部产生的细胞因子募集到子宫组织中,在那里它们促进了分娩的开始。收集小鼠子宫(i)在妊娠,TL和产后(PP)期间,(ii)在子宫内注入LPS(125μg)引发的PTL期间,或(iii)孕激素受体拮抗剂RU486的注射并分析多种细胞因子通过实时聚合酶链反应(RT-PCR)和23重细胞因子测定法检测表达水平,或酶分散以评估免疫细胞群。通过FACS评估了髓样细胞分化的标志物(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。认为:(1)TL前小鼠子宫肌层Mac升高(P <0.05),随后M和N升高;这些变化伴随着多种促炎细胞因子/趋化因子基因的增加。相应蛋白质的表达增加了PP。 (2)TL和RU486-PTL模型显示相似的基因/蛋白质表达谱,(3)LPS-PTL的特征是强烈的促炎反应和肌层组织中大量N流入,表现出与TL和RU486-PTL不同的模式, (4)在所有三个模型中,PP期都相似,子宫肌层细胞因子水平升高,免疫细胞高度浸润。我们得出的结论是,白细胞在分娩时浸润子宫肌层,暗示其在分娩激活(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。

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