Effect of Thyroid Hormone to the Expression of ATP-binding Cassette Transporter ABCG5.
- Author:
Hwa Young AHN
1
;
Jin Mi JANG
;
Kwan Jae LEE
;
Soon Hui KIM
;
Kyung Won KIM
;
Do Joon PARK
;
Hak Chul JANG
;
Young Joo PARK
Author Information
1. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea. yjparkmd@snu.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
Thyroid hormones;
ABCG5;
ABCG8;
Bile;
Cholesterol
- MeSH:
Animals;
Bile;
Cholesterol;
Hep G2 Cells;
Hepatocytes;
Homeostasis;
Humans;
Liver;
Mice;
Orphan Nuclear Receptors;
Plasmids;
Rats;
Receptors, Thyroid Hormone;
Response Elements;
Retinoid X Receptors;
RNA;
RNA, Messenger;
Thyroid Gland;
Thyroid Hormones
- From:Journal of Korean Thyroid Association
2011;4(1):39-46
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND AND OBJECTIVES: Excretion of bile acid and free cholesterol of bile was important to maintain cholesterol homeostasis. ATP-binding cassette transporter G5 (ABCG5) and G8 (ABCG8) promoted biliary cholesterol excretion. In previous study, hepatic secretion of cholesterol and ABCG5/G8 expression are strongly stimulated in hypophysectomized rats during treatment with thyroid hormone. In this study, we aimed to evaluate the effect of thyroid hormone to expression of ABCG5 and G8 in mouse liver. MATERIALS AND METHODS: We administered thyroid hormone (T3) to C57BL/6 mice and then RNA and protein was isolated from liver. We isolated primary hepatocyte and administered T3 to evaluate in vitro effect. HepG2 cells were cotransfected with either a control plasmid or expression plasmids for human thyroid hormone receptor (hTR)beta/human retinoid X receptor (hRXR)alpha or human liver X receptor (hLXR)alpha in combination with reporter plasmids TK-LXRE3-LUC with or without T3. RESULTS: Serum total cholesterol was decreased after 5 days of T3 treatment. Expression of ABCG5/8 mRNA and ABCG5 protein was increased after T3 treatment. In primary hepatocytes, T3 also increased ABCG5/8 mRNA expression. LXRalpha mRNA was not increased by T3. However, when we cotransfected liver X receptor response element (LXRE) construct and TRbeta/RXRalpha with T3, the activity of LXRE containing construct was markedly increased. CONCLUSION: We confirmed that thyroid hormone increased expression of ABCG5/8. This result suggested that thyroid hormone played an important role in decreasing serum cholesterol through bile excretion.
