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母体肥胖会刺激脂毒性,并上调足月猪胎盘的炎症信号通路。

Maternal obesity stimulates lipotoxicity and up-regulates inflammatory signaling pathways in the full-term swine placenta.

作者信息

Liang Tian, Jinglong Xie, Shusheng Dong, Aiyou Wen

机构信息

College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, China.

College of Animal Science, Xinjiang Agricultural University, Urumqi, China.

出版信息

Anim Sci J. 2018 Sep;89(9):1310-1322. doi: 10.1111/asj.13064. Epub 2018 Jun 26.

DOI:10.1111/asj.13064
PMID:29947166
Abstract

This study aimed to investigate the effects of back-fat thickness (BF), at mating of sows, on placental lipotoxicity, oxidative stress, and inflammation. We performed iTRAQ labeling-based proteomic analysis on term placentas obtained by vaginal delivery from BFI (15-20 mm, control) and BFII (21-27 mm, obese) sows formed according to BF at mating. Proteomic analysis revealed 413 proteins to be significantly different in placenta from BFII sows by ≥1.2-fold. Gene ontology (GO) analysis identified proteins related to lipid metabolism and inflammatory response to be altered in placenta from obese sows. Indicative of a lipotoxic placental environment, increased placental lipid, and up-regulated mRNA expression of lipogenic genes, including ADRP (p = .06), PPARD, FASN, ACACA, DGAT1, and LIPIN3, were associated with decreased AMPK and increased activation of WNT signaling in placenta from BFII group (p < .05). Furthermore, we observed a 18% decrease in total antioxidant capacity (TAC), increased mRNA content of pro-inflammatory cytokines IL-6, IL-18, and TNF-α, and increased activation of inflammatory NF-κB and JNK signaling in placenta from BFII sows that was significantly associated with macrophage accumulation (p < .05). These findings suggest that maternal obesity aggravates a lipotoxic environment in pig term placenta that may be associated with placental dysfunction and impaired fetal growth.

摘要

本研究旨在调查母猪配种时的背膘厚度(BF)对胎盘脂毒性、氧化应激和炎症的影响。我们对通过阴道分娩从根据配种时BF形成的BFI(15 - 20毫米,对照)和BFII(21 - 27毫米,肥胖)母猪获得的足月胎盘进行了基于iTRAQ标记的蛋白质组学分析。蛋白质组学分析显示,BFII母猪胎盘中有413种蛋白质差异显著,差异倍数≥1.2倍。基因本体(GO)分析确定,肥胖母猪胎盘中与脂质代谢和炎症反应相关的蛋白质发生了改变。BFII组胎盘脂质增加、脂肪生成基因(包括ADRP(p = 0.06)、PPARD、FASN、ACACA、DGAT1和LIPIN3)的mRNA表达上调,这表明胎盘存在脂毒性环境,与胎盘AMPK降低和WNT信号激活增加有关(p < 0.05)。此外,我们观察到BFII母猪胎盘的总抗氧化能力(TAC)降低了18%,促炎细胞因子IL - 6、IL - 18和TNF - α的mRNA含量增加,炎症NF - κB和JNK信号激活增加,这与巨噬细胞积累显著相关(p < 0.05)。这些发现表明,母体肥胖会加剧猪足月胎盘的脂毒性环境,这可能与胎盘功能障碍和胎儿生长受损有关。

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