Pitavastatin Increases ABCA1 Expression by Dual Mechanisms: SREBP2-Driven Transcriptional Activation and PPARα-Dependent Protein Stabilization but Without Activating LXR in Rat Hepatoma McARH7777 Cells
Abstract.: Hepatic ATP-binding cassette transporter A1 (ABCA1) plays a key role in high-density lipoprotein (HDL) production by apolipoprotein A-I (ApoA-I) lipidation. 3-Hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, statins, increase ABCA1 mRNA levels in hepatoma cell lines, bu...
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doaj-0f31185400da428da34cfc63b863c4052020-11-25T01:26:21ZengElsevierJournal of Pharmacological Sciences1347-86132011-01-011161107115Pitavastatin Increases ABCA1 Expression by Dual Mechanisms: SREBP2-Driven Transcriptional Activation and PPARα-Dependent Protein Stabilization but Without Activating LXR in Rat Hepatoma McARH7777 CellsTakashi Maejima0Tomohiro Sugano1Hiroyuki Yamazaki2Yasunobu Yoshinaka3Takeshi Doi4Sohei Tanabe5Tomoko Nishimaki-Mogami6Tokyo New Drug Research Laboratories, Kowa Company, Ltd., 2-17-43, Noguchicho, Higashimurayama, Tokyo 189-0022, Japan; Corresponding author. maejima-t@lsbm.orgTokyo New Drug Research Laboratories, Kowa Company, Ltd., 2-17-43, Noguchicho, Higashimurayama, Tokyo 189-0022, JapanTokyo New Drug Research Laboratories, Kowa Company, Ltd., 2-17-43, Noguchicho, Higashimurayama, Tokyo 189-0022, JapanTokyo New Drug Research Laboratories, Kowa Company, Ltd., 2-17-43, Noguchicho, Higashimurayama, Tokyo 189-0022, JapanTokyo New Drug Research Laboratories, Kowa Company, Ltd., 2-17-43, Noguchicho, Higashimurayama, Tokyo 189-0022, JapanTokyo New Drug Research Laboratories, Kowa Company, Ltd., 2-17-43, Noguchicho, Higashimurayama, Tokyo 189-0022, JapanDivision of Biosignaling, National Institute of Health Sciences, 1-18-1, Kamiyouga, Setagayaku, Tokyo 158-8501, JapanAbstract.: Hepatic ATP-binding cassette transporter A1 (ABCA1) plays a key role in high-density lipoprotein (HDL) production by apolipoprotein A-I (ApoA-I) lipidation. 3-Hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, statins, increase ABCA1 mRNA levels in hepatoma cell lines, but their mechanism of action is not yet clear. We investigated how statins increase ABCA1 in rat hepatoma McARH7777 cells. Pitavastatin, atorvastatin, and simvastatin increased total ABCA1 mRNA levels, whereas pravastatin had no effect. Pitavastatin also increased ABCA1 protein. Hepatic ABCA1 expression in rats is regulated by both liver X receptor (LXR) and sterol regulatory element–binding protein (SREBP2) pathways. Pitavastatin repressed peripheral type ABCA1 mRNA levels and its LXR-driven promoter, but activated the liver-type SREBP-driven promoter, and eventually increased total ABCA1 mRNA expression. Furthermore, pitavastatin increased peroxisome proliferator–activated receptor α (PPARα) and its downstream gene expression. Knockdown of PPARα attenuated the increase in ABCA1 protein, indicating that pitavastatin increased ABCA1 protein via PPARα activation, although it repressed LXR activation. Furthermore, the degradation of ABCA1 protein was retarded in pitavastatin-treated cells. These data suggest that pitavastatin increases ABCA1 protein expression by dual mechanisms: SREBP2-mediated mRNA transcription and PPARα-mediated ABCA1 protein stabilization, but not by the PPAR–LXR–ABCA1 pathway.[Supplementary Figures: available only at http://dx.doi.org/10.1254/jphs.10241FP] Keywords:: pitavastatin, ATP-binding cassette transporter A1 (ABCA1), sterol regulatory element–binding protein (SREBP2), peroxisome proliferator–activated receptor α (PPARα), McARH7777http://www.sciencedirect.com/science/article/pii/S1347861319307273 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Takashi Maejima Tomohiro Sugano Hiroyuki Yamazaki Yasunobu Yoshinaka Takeshi Doi Sohei Tanabe Tomoko Nishimaki-Mogami |
spellingShingle |
Takashi Maejima Tomohiro Sugano Hiroyuki Yamazaki Yasunobu Yoshinaka Takeshi Doi Sohei Tanabe Tomoko Nishimaki-Mogami Pitavastatin Increases ABCA1 Expression by Dual Mechanisms: SREBP2-Driven Transcriptional Activation and PPARα-Dependent Protein Stabilization but Without Activating LXR in Rat Hepatoma McARH7777 Cells Journal of Pharmacological Sciences |
author_facet |
Takashi Maejima Tomohiro Sugano Hiroyuki Yamazaki Yasunobu Yoshinaka Takeshi Doi Sohei Tanabe Tomoko Nishimaki-Mogami |
author_sort |
Takashi Maejima |
title |
Pitavastatin Increases ABCA1 Expression by Dual Mechanisms: SREBP2-Driven Transcriptional Activation and PPARα-Dependent Protein Stabilization but Without Activating LXR in Rat Hepatoma McARH7777 Cells |
title_short |
Pitavastatin Increases ABCA1 Expression by Dual Mechanisms: SREBP2-Driven Transcriptional Activation and PPARα-Dependent Protein Stabilization but Without Activating LXR in Rat Hepatoma McARH7777 Cells |
title_full |
Pitavastatin Increases ABCA1 Expression by Dual Mechanisms: SREBP2-Driven Transcriptional Activation and PPARα-Dependent Protein Stabilization but Without Activating LXR in Rat Hepatoma McARH7777 Cells |
title_fullStr |
Pitavastatin Increases ABCA1 Expression by Dual Mechanisms: SREBP2-Driven Transcriptional Activation and PPARα-Dependent Protein Stabilization but Without Activating LXR in Rat Hepatoma McARH7777 Cells |
title_full_unstemmed |
Pitavastatin Increases ABCA1 Expression by Dual Mechanisms: SREBP2-Driven Transcriptional Activation and PPARα-Dependent Protein Stabilization but Without Activating LXR in Rat Hepatoma McARH7777 Cells |
title_sort |
pitavastatin increases abca1 expression by dual mechanisms: srebp2-driven transcriptional activation and pparα-dependent protein stabilization but without activating lxr in rat hepatoma mcarh7777 cells |
publisher |
Elsevier |
series |
Journal of Pharmacological Sciences |
issn |
1347-8613 |
publishDate |
2011-01-01 |
description |
Abstract.: Hepatic ATP-binding cassette transporter A1 (ABCA1) plays a key role in high-density lipoprotein (HDL) production by apolipoprotein A-I (ApoA-I) lipidation. 3-Hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, statins, increase ABCA1 mRNA levels in hepatoma cell lines, but their mechanism of action is not yet clear. We investigated how statins increase ABCA1 in rat hepatoma McARH7777 cells. Pitavastatin, atorvastatin, and simvastatin increased total ABCA1 mRNA levels, whereas pravastatin had no effect. Pitavastatin also increased ABCA1 protein. Hepatic ABCA1 expression in rats is regulated by both liver X receptor (LXR) and sterol regulatory element–binding protein (SREBP2) pathways. Pitavastatin repressed peripheral type ABCA1 mRNA levels and its LXR-driven promoter, but activated the liver-type SREBP-driven promoter, and eventually increased total ABCA1 mRNA expression. Furthermore, pitavastatin increased peroxisome proliferator–activated receptor α (PPARα) and its downstream gene expression. Knockdown of PPARα attenuated the increase in ABCA1 protein, indicating that pitavastatin increased ABCA1 protein via PPARα activation, although it repressed LXR activation. Furthermore, the degradation of ABCA1 protein was retarded in pitavastatin-treated cells. These data suggest that pitavastatin increases ABCA1 protein expression by dual mechanisms: SREBP2-mediated mRNA transcription and PPARα-mediated ABCA1 protein stabilization, but not by the PPAR–LXR–ABCA1 pathway.[Supplementary Figures: available only at http://dx.doi.org/10.1254/jphs.10241FP] Keywords:: pitavastatin, ATP-binding cassette transporter A1 (ABCA1), sterol regulatory element–binding protein (SREBP2), peroxisome proliferator–activated receptor α (PPARα), McARH7777 |
url |
http://www.sciencedirect.com/science/article/pii/S1347861319307273 |
work_keys_str_mv |
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