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猪肝脏3'端定量mRNA测序揭示了不同膳食脂肪作用下未折叠蛋白反应、急性期反应以及胆固醇和胆汁酸代谢的变化。

3'quant mRNA-Seq of Porcine Liver Reveals Alterations in UPR, Acute Phase Response, and Cholesterol and Bile Acid Metabolism in Response to Different Dietary Fats.

作者信息

Oczkowicz Maria, Szmatoła Tomasz, Świątkiewicz Małgorzata, Koseniuk Anna, Smołucha Grzegorz, Witarski Wojciech, Wierzbicka Alicja

机构信息

Department of Animal Molecular Biology, National Research Institute of Animal Production, ul Krakowska 1, 32-083 Balice, Poland.

Centre of Experimental and Innovative Medicine, University of Agriculture in Kraków, Al. Mickiewicza 24/28, 30-059 Kraków, Poland.

出版信息

Genes (Basel). 2020 Sep 18;11(9):1087. doi: 10.3390/genes11091087.

DOI:10.3390/genes11091087
PMID:32961898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7565913/
Abstract

Animal fats are considered to be unhealthy, in contrast to vegetable fats, which are rich in unsaturated fatty acids. However, the use of some fats, such as coconut oil, is still controversial. In our experiment, we divided experimental animals (domestic pigs) into three groups differing only in the type of fat used in the diet: group R: rapeseed oil ( = 5); group B: beef tallow ( = 5); group C: coconut oil ( = 6). After transcriptomic analysis of liver samples, we identified 188, 93, and 53 DEGs (differentially expressed genes) in R vs. B, R vs. C, and B vs. C comparisons, respectively. Next, we performed a functional analysis of identified DEGs with String and IPA software. We observed the enrichment of genes engaged in the unfolded protein response (UPR) and the acute phase response among genes upregulated in B compared to R. In contrast, cholesterol biosynthesis and cholesterol efflux enrichments were observed among genes downregulated in B when compared to R. Moreover, activation of the UPR and inhibition of the sirtuin signaling pathway were noted in C when compared to R. The most striking difference in liver transcriptomic response between C and B was the activation of the acute phase response and inhibition of bile acid synthesis in the latest group. Our results suggest that excessive consumption of animal fats leads to the activation of a cascade of mutually propelling processes harmful to the liver: inflammation, UPR, and imbalances in the biosynthesis of cholesterol and bile acids via altered organelle membrane composition. Nevertheless, these studies should be extended with analysis at the level of proteins and their function.

摘要

与富含不饱和脂肪酸的植物油相比,动物脂肪被认为是不健康的。然而,某些脂肪(如椰子油)的使用仍然存在争议。在我们的实验中,我们将实验动物(家猪)分为三组,仅饮食中使用的脂肪类型不同:R组:菜籽油(n = 5);B组:牛脂(n = 5);C组:椰子油(n = 6)。对肝脏样本进行转录组分析后,我们在R与B、R与C以及B与C的比较中分别鉴定出188、93和53个差异表达基因(DEG)。接下来,我们使用String和IPA软件对鉴定出的DEG进行功能分析。我们观察到,与R组相比,B组上调的基因中参与未折叠蛋白反应(UPR)和急性期反应的基因富集。相反,与R组相比,B组下调的基因中观察到胆固醇生物合成和胆固醇流出的富集。此外,与R组相比,C组中观察到UPR的激活和沉默调节蛋白信号通路的抑制。C组和B组肝脏转录组反应最显著的差异是急性期反应的激活和后一组中胆汁酸合成的抑制。我们的结果表明,过量食用动物脂肪会导致一系列对肝脏有害的相互促进过程的激活:炎症、UPR以及通过改变细胞器膜组成导致胆固醇和胆汁酸生物合成失衡。然而,这些研究应在蛋白质及其功能水平上进行分析加以扩展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/fca5037bd415/genes-11-01087-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/14509d5ff788/genes-11-01087-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/9d009bf938d0/genes-11-01087-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/b8c6f69dde36/genes-11-01087-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/a146f9788cde/genes-11-01087-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/a14f68bf2c37/genes-11-01087-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/e655aaf94288/genes-11-01087-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/fca5037bd415/genes-11-01087-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/14509d5ff788/genes-11-01087-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/b881964ac7a9/genes-11-01087-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/33b795046380/genes-11-01087-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/9d009bf938d0/genes-11-01087-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/b8c6f69dde36/genes-11-01087-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/a146f9788cde/genes-11-01087-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/a14f68bf2c37/genes-11-01087-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/e655aaf94288/genes-11-01087-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b298/7565913/fca5037bd415/genes-11-01087-g009.jpg

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