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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Main Authors: Takashi Maejima, Tomohiro Sugano, Hiroyuki Yamazaki, Yasunobu Yoshinaka, Takeshi Doi, Sohei Tanabe, Tomoko Nishimaki-Mogami
Format: Article
Language:English
Published: Elsevier 2011-01-01
Series:Journal of Pharmacological Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S1347861319307273
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spelling 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
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