Disruption of ESR1 alters the expression of genes regulating hepatic lipid and carbohydrate metabolism in male rats. (15th June 2019)

• Record Type: Journal Article
• Authors: Khristi, Vincentaben; Ratri, Anamika; Ghosh, Subhra; Pathak, Devansh; Borosha, Shaon; Dai, Eddie; Roy, Richita; Chakravarthi, V. Praveen; Wolfe, Michael W.; Karim Rumi, M.A.
• Is Part Of: Molecular and cellular endocrinology. Volume 490(2019)
• Page Start: 47
• Page End: 56
• Publication Date: 2019-06-15
• Subjects: ESR1 -- Liver -- Transcriptome analyses -- Lipid and carbohydrate metabolism; Endocrinology -- Periodicals; Molecular biology -- Periodicals; Cytology -- Periodicals; Endocrinology -- Periodicals; Hormones -- Periodicals; Endocrinologie -- Périodiques; Cytology; Endocrinology; Molecular biology; Periodicals; 573.4
• DOI: 10.1016/j.mce.2019.04.005
• Languages: English
• ISSNs: 0303-7207

Abstract

Abstract: The liver helps maintain energy homeostasis by synthesizing and storing glucose and lipids. Gonadal steroids, particularly estrogens, play an important role in regulating metabolism. As estrogens are considered female hormones, metabolic disorders related to the disruption of estrogen signaling have mostly been studied in females. Estrogen receptor alpha (ESR1) is the predominant receptor in both the male and female liver, and it mediates the hepatic response to estrogens. Loss of ESR1 increases weight gain and obesity in female rats, while reducing the normal growth in males. Although Esr1−/− male rats have a reduced body weight, they exhibit increased adipose deposition and impaired glucose tolerance. We further investigated whether these metabolic disorders in Esr1−/− male rats were linked with the loss of transcriptional regulation by ESR1 in the liver. To identify the ESR-regulated genes, RNA-sequencing was performed on liver mRNAs from wildtype and Esr1−/− male rats. Based on an absolute fold change of ≥2 with a p-value ≤ 0.05, a total of 706 differentially expressed genes were identified in the Esr1−/− male liver: 478 downregulated, and 228 upregulated. Pathway analyses demonstrate that the differentially expressed genes include transcriptional regulators ( Cry1, Nr1d1, Nr0b2 ), transporters ( Slc1a2 ), and regulators of biosynthesis ( Cyp7b1, Cyp8b1 ), and hormone metabolism ( Hsd17b2, Sult1e1 ). Many of these genes are also integral parts of the lipid and carbohydrate metabolism pathways in the liver. Interestingly, certain critical regulators of the metabolic pathways displayed a sexual dimorphism in expression, which may explain the divergent weight gain in Esr1−/− male and female rats despite common metabolic dysfunctions. Highlights: Estrogen receptor 1 (ESR1) is essential for hepatic lipid and carbohydrate metabolism. RNA-seq analyses identified differentially expressed genes in Esr1−/− liver tissues. 706 differentially expressed genes were detected in Esr1 null liver, 478 downregulated and 228 upregulated. Disruption of ESR1 deregulated key genes involved in hepatic lipid, and carbohydrate metabolism. Sexual dimorphism of certain metabolic regulators may explain the divergent weight gain in Esr1−/− male and female rats.