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全血转录组分析揭示了负能平衡和对炎症挑战的反应之间代谢途径的潜在竞争。

Whole blood transcriptome analysis reveals potential competition in metabolic pathways between negative energy balance and response to inflammatory challenge.

机构信息

INRA, UMR1388 Génétique, Physiologie et Systèmes d'Elevage, F-31326, Castanet-Tolosan, France.

Université de Toulouse, École Nationale Vétérinaire de Toulouse (ENVT), INRA, Interactions Hôtes - Agents Pathogènes (IHAP), F-31076, Toulouse, France.

出版信息

Sci Rep. 2017 May 24;7(1):2379. doi: 10.1038/s41598-017-02391-y.

Abstract

Negative Energy Balance (NEB) is considered to increase susceptibility to mastitis. The objective of this study was to improve our understanding of the underlying mechanisms by comparing transcriptomic profiles following NEB and a concomitant mammary inflammation. Accordingly, we performed RNA-seq analysis of blood cells in energy-restricted ewes and control-diet ewes at four different time points before and after intra mammary challenge with phlogogenic ligands. Blood leucocytes responded to NEB by shutting down lipid-generating processes, including cholesterol and fatty acid synthesis, probably under transcriptional control of SREBF 1. Furthermore, fatty acid oxidation was activated and glucose oxidation and transport inhibited in response to energy restriction. Among the differentially expressed genes (DEGs) in response to energy restriction, 64 genes were also differential in response to the inflammatory challenge. Opposite response included the activation of cholesterol and fatty acid synthesis during the inflammatory challenge. Moreover, activation of glucose oxidation and transport coupled with the increase of plasma glucose concentration in response to the inflammatory stimuli suggested a preferential utilization of glucose as the energy source during this stress. Leucocyte metabolism therefore undergoes strong metabolic changes during an inflammatory challenge, which could be in competition with those induced by energy restriction.

摘要

负能平衡(NEB)被认为会增加乳腺炎的易感性。本研究的目的是通过比较 NEB 和同时发生的乳腺炎后的转录组谱,来更好地理解潜在的机制。因此,我们在能量限制的母羊和对照饮食的母羊中进行了四个不同时间点的血液细胞 RNA-seq 分析,这些时间点是在乳腺内用致炎配体刺激之前和之后。血液白细胞通过关闭脂质生成过程(包括胆固醇和脂肪酸合成)来应对 NEB,这可能受到 SREBF1 的转录控制。此外,脂肪酸氧化被激活,葡萄糖氧化和转运受到能量限制的抑制。在能量限制下表达差异的基因(DEGs)中,有 64 个基因也对炎症挑战有差异反应。相反的反应包括在炎症挑战期间胆固醇和脂肪酸合成的激活。此外,对炎症刺激的葡萄糖氧化和转运的激活以及血浆葡萄糖浓度的增加表明,在这种应激下,葡萄糖优先被用作能量来源。因此,白细胞代谢在炎症挑战期间会发生强烈的代谢变化,这可能与能量限制引起的变化相竞争。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d3a/5443788/b47dbb64f127/41598_2017_2391_Fig1_HTML.jpg

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