24S-hydroxycholesterol induces cholesterol release from choroid plexus epithelial cells in an apical- and apoE isoform-dependent manner concomitantly with the induction of ABCA1 and ABCG1 expression

Masachika Fujiyoshi, Sumio Ohtsuki, Satoko Hori, Masanori Tachikawa, Tetsuya Terasaki

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

The release of cholesterol from choroid plexus epithelial cells (CPE) plays an important role in cholesterol homeostasis in the CSF. The purpose of this study was to clarify the molecules involved in cholesterol release in CPE and the regulation mechanisms of the cholesterol release by the liver X receptor (LXR) using a conditionally immortalized CPE line (TR-CSFB3). The mRNA expression of LXRα, LXRβ and their target genes, ATP-binding cassette transporter (ABC)A1, ABCG1, ABCG4 and ABCG5, were detected in rat choroid plexus. ABCA1 and ABCG1 protein were detected in the plasma membrane of TR-CSFB3 cells. Following treatment with 24S-hydroxycholesterol, an endogenous LXR ligand, the expression of ABCA1 and ABCG1 were induced in TR-CSFB3 cells. Moreover, apolipoprotein (apo)AI- and high-density lipoprotein (HDL)-mediated cholesterol release to the apical side of TR-CSFB3 cells was facilitated by this treatment, whereas that to the basal side was not affected. Following 24S-hydroxycholesterol treatment, apoE3-dependent cholesterol release from TR-CSFB3 cells was enhanced more than the apoE4-dependent release. These results suggest that LXR activation facilitates cholesterol release into the CSF from CPE through the functional induction of ABCA1 and ABCG1. The difference between apoE3 and apoE4 suggests that the cholesterol release from CPE is related to the development of neurodegenerative diseases.

Original languageEnglish
Pages (from-to)968-978
Number of pages11
JournalJournal of Neurochemistry
Volume100
Issue number4
DOIs
Publication statusPublished - Feb 1 2007
Externally publishedYes

Fingerprint

Choroid Plexus
Apolipoproteins E
Protein Isoforms
Epithelial Cells
Cholesterol
Liver
Apolipoprotein E3
Apolipoprotein E4
ATP Binding Cassette Transporter 1
Neurodegenerative diseases
ATP-Binding Cassette Transporters
Apolipoprotein A-I
24-hydroxycholesterol
Neurodegenerative Diseases
HDL Cholesterol
HDL Lipoproteins
Cell membranes
Homeostasis
Rats
Cell Membrane

Keywords

  • 24S-hydroxycholesterol
  • ABCA1
  • ABCG1
  • Cholesterol
  • Choroid plexus epithelial cells
  • Liver X receptor

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

Cite this

24S-hydroxycholesterol induces cholesterol release from choroid plexus epithelial cells in an apical- and apoE isoform-dependent manner concomitantly with the induction of ABCA1 and ABCG1 expression. / Fujiyoshi, Masachika; Ohtsuki, Sumio; Hori, Satoko; Tachikawa, Masanori; Terasaki, Tetsuya.

In: Journal of Neurochemistry, Vol. 100, No. 4, 01.02.2007, p. 968-978.

Research output: Contribution to journalArticle

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abstract = "The release of cholesterol from choroid plexus epithelial cells (CPE) plays an important role in cholesterol homeostasis in the CSF. The purpose of this study was to clarify the molecules involved in cholesterol release in CPE and the regulation mechanisms of the cholesterol release by the liver X receptor (LXR) using a conditionally immortalized CPE line (TR-CSFB3). The mRNA expression of LXRα, LXRβ and their target genes, ATP-binding cassette transporter (ABC)A1, ABCG1, ABCG4 and ABCG5, were detected in rat choroid plexus. ABCA1 and ABCG1 protein were detected in the plasma membrane of TR-CSFB3 cells. Following treatment with 24S-hydroxycholesterol, an endogenous LXR ligand, the expression of ABCA1 and ABCG1 were induced in TR-CSFB3 cells. Moreover, apolipoprotein (apo)AI- and high-density lipoprotein (HDL)-mediated cholesterol release to the apical side of TR-CSFB3 cells was facilitated by this treatment, whereas that to the basal side was not affected. Following 24S-hydroxycholesterol treatment, apoE3-dependent cholesterol release from TR-CSFB3 cells was enhanced more than the apoE4-dependent release. These results suggest that LXR activation facilitates cholesterol release into the CSF from CPE through the functional induction of ABCA1 and ABCG1. The difference between apoE3 and apoE4 suggests that the cholesterol release from CPE is related to the development of neurodegenerative diseases.",
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