High-fat diet and estrogen impacts the colon and its transcriptome in a sex-dependent manner

被引:30
|
作者
Hases, L. [1 ,2 ]
Archer, A. [1 ,2 ]
Indukuri, R. [1 ,2 ]
Birgersson, M. [1 ,2 ]
Savva, C. [3 ,4 ,5 ]
Korach-Andr, M. [3 ,4 ,5 ]
Williams, C. [1 ,2 ]
机构
[1] KTH Royal Inst Technol, Dept Prot Sci, Sci Life Lab, Solna, Sweden
[2] Karolinska Inst, Dept Biosci & Nutr, Huddinge, Sweden
[3] Karolinska Inst, Dept Med, Metab Unit, Stockholm, Sweden
[4] Karolinska Inst, Integrated CardioMetab Ctr ICMC, Stockholm, Sweden
[5] Karolinska Univ Hosp Huddinge, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
TUMOR-NECROSIS-FACTOR; RECEPTOR-BETA; COLORECTAL-CANCER; INDUCED OBESITY; ADIPOSE-TISSUE; INSULIN-RESISTANCE; ALPHA; METAANALYSIS; RISK; TUMORIGENESIS;
D O I
10.1038/s41598-020-73166-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
There is a strong association between obesity and colorectal cancer (CRC), especially in men, whereas estrogen protects against both the metabolic syndrome and CRC. Colon is the first organ to respond to high-fat diet (HFD), and estrogen receptor beta (ER beta) can attenuate CRC development. How estrogen impacts the colon under HFD and related sex differences has, however, not been investigated. To dissect this, mice were fed control diet or HFD for 13 weeks and administered receptor-selective estrogenic ligands for the last three weeks. We recorded impact on metabolism, colon crypt proliferation, macrophage infiltration, and the colon transcriptome. We found clear sex differences in the colon transcriptome and in the impact by HFD and estrogens, including on clock genes. ER alpha-selective activation reduced body weight and generated systemic effects, whereas ER beta-selective activation had local effects in the colon, attenuating HFD-induced macrophage infiltration and epithelial cell proliferation. We here demonstrate how HFD and estrogens modulate the colon microenvironment in a sex- and ER-specific manner.
引用
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页数:13
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