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牙龈卟啉单胞菌外膜囊泡重塑滋养层细胞代谢,损害与不良妊娠结局相关的功能。

Porphyromonas gingivalis outer membrane vesicles shape trophoblast cell metabolism impairing functions associated to adverse pregnancy outcome.

机构信息

Universidad de Buenos Aires - CONICET, Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), Laboratorio de Inmunofarmacología, Buenos Aires, Argentina.

Universidad de Buenos Aires - Facultad de Odontología, Cátedra de Microbiología, Buenos Aires, Argentina.

出版信息

J Cell Physiol. 2023 Nov;238(11):2679-2691. doi: 10.1002/jcp.31138. Epub 2023 Oct 16.

Abstract

Periodontitis is proposed as a risk factor for preterm delivery, fetal growth restriction, and preeclampsia with severe consequences for maternal and neonatal health, but the biological mechanisms involved are elusive. Porphyromonas gingivalis gain access to the placental bed and impair trophoblast cell function, as assessed in murine and human pregnancy, suggesting a pathogenic role in adverse pregnancy and neonatal outcomes. P. gingivalis releases outer membrane vesicles (P. gingivalis OMV) during growth that spread to distant tissues and are internalized in host cells as described in metabolic, neurological, and vascular systemic diseases. Here we tested the hypothesis that P. gingivalis OMV internalized in trophoblast cells disrupt their metabolism leading to trophoblast and placenta dysfunction and adverse pregnancy outcomes. An in vitro design with human trophoblast cells incubated with P. gingivalis OMV was used together with ex vivo and in vivo approaches in pregnant mice treated with P. gingivalis OMV. P. gingivalis OMV modulated human trophoblast cell metabolism by reducing glycolytic pathways and decreasing total reactive oxygen species with sustained mitochondrial activity. Metabolic changes induced by P. gingivalis OMV did not compromise cell viability; instead, it turned trophoblast cells into a metabolic resting state where central functions such as migration and invasion were reduced. The effects of P. gingivalis OMV on human trophoblast cells were corroborated ex vivo in mouse whole placenta and in vivo in pregnant mice: P. gingivalis OMV reduced glycolytic pathways in the placenta and led to lower placental and fetal weight gain in vivo with reduced placental expression of the glucose transporter GLUT1. The present results point to OMV as a key component of P. gingivalis involved in adverse pregnancy outcomes, and even more, unveil a metabolic cue in the deleterious effect of P. gingivalis OMV on trophoblast cells and mouse pregnancy, providing new clues to understand pathogenic mechanisms in pregnancy complications and other systemic diseases.

摘要

牙周炎被认为是早产、胎儿生长受限和子痫前期的危险因素,这些疾病对母婴健康都有严重影响,但其中涉及的生物学机制尚不清楚。牙龈卟啉单胞菌进入胎盘床并损害滋养层细胞功能,这在鼠类和人类妊娠中得到了评估,表明其在不良妊娠和新生儿结局中具有致病性作用。在生长过程中,牙龈卟啉单胞菌会释放出外膜囊泡(P. gingivalis OMV),这些囊泡会扩散到远处的组织,并被宿主细胞内化,这在代谢、神经和血管系统疾病中已有描述。在这里,我们检验了这样一个假设,即被内化到滋养层细胞中的牙龈卟啉单胞菌 OMV 会破坏其代谢功能,导致滋养层和胎盘功能障碍以及不良的妊娠结局。我们采用了一种体外设计,用人滋养层细胞孵育牙龈卟啉单胞菌 OMV,同时在接受牙龈卟啉单胞菌 OMV 处理的妊娠小鼠中采用了离体和体内方法。牙龈卟啉单胞菌 OMV 通过降低糖酵解途径和减少总活性氧来调节人滋养层细胞的代谢,同时保持线粒体活性。牙龈卟啉单胞菌 OMV 诱导的代谢变化不会损害细胞活力;相反,它使滋养层细胞进入一种代谢静止状态,其中迁移和侵袭等核心功能会减弱。在体外培养的小鼠整个胎盘和体内妊娠小鼠中,都证实了牙龈卟啉单胞菌 OMV 对人滋养层细胞的影响:牙龈卟啉单胞菌 OMV 降低了胎盘的糖酵解途径,导致体内胎盘和胎儿体重增加减少,同时胎盘葡萄糖转运蛋白 GLUT1 的表达减少。本研究结果表明,OMV 是牙龈卟啉单胞菌参与不良妊娠结局的关键成分,甚至揭示了 OMV 对滋养层细胞和小鼠妊娠的有害影响中的一种代谢信号,为理解妊娠并发症和其他系统性疾病的致病机制提供了新的线索。

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