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肥胖和饮食独立影响小鼠的母体免疫、母体肠道微生物群和妊娠结局。

Obesity and diet independently affect maternal immunity, maternal gut microbiota and pregnancy outcome in mice.

机构信息

Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.

Department of Obstetrics and Gynaecology, Erasmus University Medical Center, Rotterdam, Netherlands.

出版信息

Front Immunol. 2024 Jul 12;15:1376583. doi: 10.3389/fimmu.2024.1376583. eCollection 2024.

Abstract

INTRODUCTION

Maternal obesity poses risks for both mother and offspring during pregnancy, with underlying mechanisms remaining largely unexplored. Obesity is associated with microbial gut dysbiosis and low-grade inflammation, and also the diet has a major impact on these parameters. This study aimed to investigate how maternal obesity and diet contribute to changes in immune responses, exploring potential associations with gut microbiota dysbiosis and adverse pregnancy outcomes in mice.

METHODS

Before mating, C57BL/6 mice were assigned to either a high-fat-diet (HFD) or low-fat-diet (LFD) to obtain obese (n=17) and lean (n=10) mice. To distinguish between the effects of obesity and diet, 7 obese mice were switched from the HFD to the LFD from day 7 until day 18 of pregnancy ("switch group"), which was the endpoint of the study. T helper (Th) cell subsets were studied in the spleen, mesenteric lymph nodes (MLN) and Peyer's patches (PP), while monocyte subsets and activation status were determined in maternal blood (flow cytometry). Feces were collected before and during pregnancy (day 7,14,18) for microbiota analysis (16S rRNA sequencing). Pregnancy outcome included determination of fetal and placental weight.

RESULTS

Obesity increased splenic Th1 and regulatory T cells, MLN Th1 and PP Th17 cells and enhanced IFN-γ and IL-17A production by splenic Th cells upon ex vivo stimulation. Switching diet decreased splenic and PP Th2 cells and classical monocytes, increased intermediate monocytes and activation of intermediate/nonclassical monocytes. Obesity and diet independently induced changes in the gut microbiota. Various bacterial genera were increased or decreased by obesity or the diet switch. These changes correlated with the immunological changes. Fetal weight was lower in the obese than the lean group, while placental weight was lower in the switch than the obese group.

DISCUSSION

This study demonstrates that obesity and diet independently impact peripheral and intestinal immune responses at the end of pregnancy. Simultaneously, both factors affect specific bacterial gut genera and lead to reduced fetal or placental weight. Our data suggest that switching diet during pregnancy to improve maternal health is not advisable and it supports pre/probiotic treatment of maternal obesity-induced gut dysbiosis to improve maternal immune responses and pregnancy outcome.

摘要

简介

母亲肥胖在怀孕期间对母亲和胎儿都有风险,但其潜在机制在很大程度上仍未得到探索。肥胖与肠道微生物失调和低度炎症有关,而饮食也对这些参数有重大影响。本研究旨在探讨母体肥胖和饮食如何导致免疫反应的变化,探索其与肠道微生物失调和不良妊娠结局的潜在关联。

方法

在交配前,将 C57BL/6 小鼠分为高脂肪饮食(HFD)或低脂肪饮食(LFD)组,以获得肥胖(n=17)和瘦(n=10)小鼠。为了区分肥胖和饮食的影响,将 7 只肥胖小鼠从 HFD 转换为 LFD,从妊娠第 7 天持续到第 18 天(“转换组”),这是研究的终点。在脾脏、肠系膜淋巴结(MLN)和派尔氏斑(PP)中研究辅助性 T 细胞亚群,通过流式细胞术在母血中测定单核细胞亚群和激活状态。在妊娠前和妊娠期间(第 7、14、18 天)收集粪便进行微生物分析(16S rRNA 测序)。妊娠结局包括确定胎儿和胎盘重量。

结果

肥胖增加了脾脏 Th1 和调节性 T 细胞、MLN Th1 和 PP Th17 细胞,并增强了脾脏 Th 细胞体外刺激后的 IFN-γ和 IL-17A 产生。饮食转换减少了脾脏和 PP Th2 细胞和经典单核细胞,增加了中间单核细胞和中间/非经典单核细胞的激活。肥胖和饮食独立地诱导了肠道微生物群的变化。肥胖或饮食转换增加或减少了各种细菌属。这些变化与免疫学变化相关。与瘦组相比,肥胖组胎儿体重较低,与肥胖组相比,转换组胎盘重量较低。

讨论

本研究表明,肥胖和饮食在妊娠末期独立影响外周和肠道免疫反应。同时,这两个因素都影响特定的肠道细菌属,并导致胎儿或胎盘重量降低。我们的数据表明,在怀孕期间转换饮食以改善母体健康是不可取的,它支持母体肥胖诱导的肠道菌群失调的预/益生菌治疗,以改善母体免疫反应和妊娠结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5acd/11272480/2818b0252f5f/fimmu-15-1376583-g001.jpg

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