Placental interleukin 1β signaling in canine pregnancy: differential effects during and after decidualization in vitro.

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Reproduction Pub Date : 2025-03-26 Print Date: 2025-04-01 DOI:10.1530/REP-24-0470
Miguel Tavares Pereira, Selim Aslan, Rita Payan-Carreira, Iris M Reichler, Karine Reynaud, Mariusz P Kowalewski
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引用次数: 0

Abstract

In brief: The role of inflammation in the regulation of pregnancy remains poorly understood in dogs. Findings from this study propose the involvement of IL1β signaling during early embryo-maternal interactions in the dog, while in vitro effects suggest it may disrupt decidual cell function in the canine mature placenta.

Abstract: Although implantation and parturition are associated with pro-inflammatory signals, inflammatory responses in the mature placenta frequently lead to pregnancy loss. Indeed, uterine inflammatory/infectious diseases are major causes of infertility and pregnancy loss in dogs. The pro-inflammatory interleukin (IL)-1β is increased during canine placentation and downregulated in mature placentae during healthy pregnancies but is enriched in the placenta during infectious events. Furthermore, canine pregnancy success is linked with decidual cells, the only placental cells expressing the nuclear progesterone receptor. This study assessed utero-placental abundance of IL1β receptor 1 (IL1R1) throughout canine pregnancy and possible modulatory effects of IL1β on decidualization. The mRNA levels of IL1R1 were increased in mature mid-gestation placentae and at term (P < 0.05). Immunohistochemistry co-localized IL1β and IL1R1 in the trophoblast during early placentation, implicating IL1β-signaling in early embryo-maternal communication. In the mature placenta, IL1R1 was localized, i.a. in decidual cells. In vitro, IL1β had low modulatory effects on PGE2- and/or P4-stimulated dog uterine stromal (DUS) cells, implying a relatively weak impact of this interleukin in the decidualization process. However, in DUS cells decidualized with cAMP, IL1β decreased transcriptional amounts of selected decidualization markers IGF1, PTGS2 and PTGES, as well as ECM1 and TIMP2 (P < 0.001). Transcriptional and protein availabilities of CX43, a gap junction component, were also decreased by IL1β (P < 0.001). These findings support a dual role for IL1β in canine pregnancy: involvement in early embryo-maternal communication during its establishment and disturbing placental homeostasis by disrupting decidual cell function in fully developed placenta.

胎盘白介素1β信号在犬妊娠中的作用:体外脱胎化期间和之后的差异效应。
虽然着床和分娩与促炎信号有关,但成熟胎盘中的炎症反应经常导致妊娠丢失。事实上,子宫炎症/传染病是狗不育和流产的主要原因。促炎白细胞介素(IL)-1β在犬胎盘中升高,在健康妊娠期间成熟胎盘中下调,但在感染事件期间胎盘中富集。此外,犬的怀孕成功与蜕细胞有关,蜕细胞是唯一表达核孕酮受体的胎盘细胞。本研究评估了犬孕期子宫胎盘中il - 1β受体1 (IL1R1)的丰度,以及il - 1β对去个体化的可能调节作用。il - 1r1 mRNA水平在妊娠中期和足月时均升高(P < 0.05)。免疫组织化学在胎盘早期滋养细胞中共同定位il - 1β和il - 1r1,暗示il - 1β信号在早期胚胎-母体通讯中起作用。在成熟胎盘中,IL1R1定位于蜕细胞中。在体外,il - 1β对PGE2-和/或p4刺激的狗子宫间质(DUS)细胞具有低调节作用,这意味着这种白细胞介素在去细胞化过程中的影响相对较弱。然而,在使用cAMP进行去个体化的DUS细胞中,il - 1β降低了所选择的去个体化标记物IGF1、PTGS2和PTGES以及ECM1和TIMP2的转录量(P < 0.001)。间隙连接成分CX43的转录和蛋白质有效性也被il - 1β降低(P < 0.001)。这些发现支持il - 1β在犬妊娠中的双重作用:参与早期胚胎-母体在其建立过程中的交流,并通过破坏完全发育的胎盘中的蜕细胞功能来扰乱胎盘稳态。
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来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
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