无菌小鼠胎盘内分泌功能受母体肠道双歧杆菌控制。

IF 7.5 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Jorge Lopez-Tello, Raymond Kiu, Zoe Schofield, Matthew J Dalby, Douwe van Sinderen, Gwénaëlle Le Gall, Lindsay J Hall, Amanda N Sferruzzi-Perri
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引用次数: 0

摘要

背景:最近的研究表明,母体肠道微生物群可以调节胎盘生长,特别是运输区,并与胎儿生长有关。然而,某些微生物在调节胎盘激素产生中的具体作用,对支持胎儿发育和维持健康妊娠至关重要,仍未得到充分研究。在这种背景下,本研究的目的是确定母体与早期肠道细菌短双歧杆菌UCC2003的定植是否调节胎盘内分泌功能。方法:将无菌妊娠小鼠在妊娠期间分别定殖短双歧杆菌UCC2003 (BIF)和不定植短双歧杆菌(BIF)。收集胎盘内分泌区(交界区,Jz)的代谢特征,采用代谢组学方法分析其代谢特征,采用qPCR方法分析其关键营养摄取基因、激素和合成基因的表达,采用LC-MS/MS方法分析其蛋白质组学特征。结果:BIF定殖的母鼠胎盘Jz中乳酸和牛磺酸浓度升高。BIF的存在还与营养载体的表达上调有关,特别是那些参与大中性氨基酸和单羧酸盐摄取的载体(如Slc7a8和Slc16a4)。此外,关键激素,如催乳素和妊娠特异性糖蛋白,上调。在BIF定植的水坝中,Jz蛋白质组发生了变化,有超过400种蛋白质失调。通路分析显示,超过150个生物过程发生了改变,包括转录活性、蛋白质合成、细胞周期进程和代谢调节。胎盘Jz中受BIF调控的蛋白与胎儿生长和营养水平(即葡萄糖)相关。值得注意的是,母亲相关的BIF减少了胎儿吸收的数量(早期胎儿丢失)。结论:在无菌小鼠中,母体相关的肠道短双歧杆菌UCC2003通过改变其代谢谱和产生内分泌因子的能力来调节胎盘内分泌能力。本研究首次提供了明确的证据,表明母体肠道微生物群不仅影响胎盘转运功能,还调节其内分泌输出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Placental endocrine function is controlled by maternal gut Bifidobacterium in germ-free mice.

Background: Recent studies have shown that the maternal gut microbiota can regulate placental growth, particularly the transport region, in association with fetal growth. However, the specific role of certain microorganisms in modulating the hormonal production of the placenta, which is critical for supporting fetal development and maintaining a healthy pregnancy, remains largely unexplored. In this context, the objective of this study is to determine whether the maternal colonisation with the early life gut bacterium Bifidobacterium breve UCC2003 regulates placental endocrine function.

Methods: Pregnant germ-free mice were colonized with or without Bifidobacterium breve UCC2003 (BIF) during pregnancy. The endocrine region of the placenta (junctional zone, Jz) was collected to assess its metabolic profile using metabolomics, the expression of key nutrient uptake genes, hormones and synthetic genes by qPCR, and proteome using LC-MS/MS.

Results: BIF colonised dams had increased lactate and taurine concentrations in the placental Jz. BIF presence was also associated with upregulated expression of nutrient carriers, particularly those involved in large neutral amino acid and monocarboxylate uptake (e.g., Slc7a8 and Slc16a4). Additionally, key hormones, such as prolactins and pregnancy-specific glycoproteins, were upregulated. The Jz proteome was changed in BIF colonised dams, with over 400 proteins dysregulated. Pathway analysis revealed more than 150 biological processes were altered, including transcriptional activity, protein synthesis, cell cycle progression, and metabolic regulation. Proteins regulated by BIF in the placental Jz were correlated with fetal growth and nutrient levels (namely glucose). Notably, maternal-associated BIF reduced the number of fetal resorptions (early fetal loss).

Conclusions: In germ-free mice, maternal-associated gut Bifidobacterium breve UCC2003 regulates placental endocrine capacity, by altering its metabolic profile and ability to produce endocrine factors. This study provides the first clear evidence that the maternal gut microbiota not only influences placental transport function, but also regulates its endocrine outputs.

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来源期刊
Journal of Translational Medicine
Journal of Translational Medicine 医学-医学:研究与实验
CiteScore
10.00
自引率
1.40%
发文量
537
审稿时长
1 months
期刊介绍: The Journal of Translational Medicine is an open-access journal that publishes articles focusing on information derived from human experimentation to enhance communication between basic and clinical science. It covers all areas of translational medicine.
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