Cited by 184Cholesterol and Lipid MetabolismDrug Transport and Resistance MechanismsLipoproteins and Cardiovascular Health

ATP‐binding cassette transporters G1 and G4 mediate cholesterol and desmosterol efflux to HDL and regulate sterol accumulation in the brain

Wang, Nan, Yvan‐Charvet, Laurent, Lütjohann, Dieter, Mulder, Monique, Vanmierlo, Tim, Kim, Tae‐Wan, Tall, Alan R.·2008·The FASEB Journal

Abstract

Transporters in the ABCG family appear to be involved in the cellular excretion of cholesterol and other sterols in a cell‐ and tissue‐specific fashion. Overexpression of ATP‐binding cassette transporters G1 (Abcgl) and G4 (Abcg4) can promote cellular cholesterol efflux to high‐density lipoprotein (HDL), but the in vivo functions of Abcg4 are poorly understood. We used mice with knockouts of Abcgl or Abcg4 singly or together to further elucidate the function of these transporters. Abcg1 and Abcg4 are highly expressed in the brain and are found in both astrocytes and neurons. Whereas Abcgl _/_ or Abcg4 _/_ mice showed essentially normal levels of brain sterols, in Abcgl _/_ /Abcg4 _/_ mice, levels of several sterol intermediates in the cholesterol biosynthetic pathway, namely desmosterol, lathosterol, and lanosterol, as well as 27‐OH cholesterol, were increased 2‐ to 3‐fold. Overexpression of Abcgl or Abcg4 promoted efflux of desmosterol and cholesterol from cells to HDL, and combined deficiency of these transporters led to defective efflux and accumulation of these sterols in primary astrocytes. Consistent with defective efflux and sterol accumulation, cholesterol biosynthesis was reduced in Abcgl _/_ /Abcg4 _/_ astrocytes. The accumulation of desmosterol, a known liver‐X receptor (LXR) activator, was associated with increased expression of LXR target genes, including ATP‐binding cassette transporter Al, and increased apolipoprotein E secretion in Abcgl _/_ / Abcg4 _/_ astrocytes. Our findings provide the first in vivo demonstration of a role for Abcg4 in sterol efflux in the brain and show that Abcgl and Abcg4 have overlapping functions in astrocytes, promoting efflux of cholesterol, desmosterol, and possibly other sterol biosynthetic intermediates to HDL. Wang, N., Yvan‐Charvet, L., Lutjohann, D., Mulder, M., Vanmierlo, T., Kim, T.‐W., Tall, A. R ATP‐binding cassette transporters Gl and G4 mediate cholesterol and desmosterol efflux to HDL and regulate sterol accumulation in the brain. FASEB J. 22, 1073–1082 (2008)

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Crossref · 10.1096/fj.07-9944com

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Authors
Wang, N., Yvan‐Charvet, L., Lütjohann, D., Mulder, M., Vanmierlo, T., Kim, T., & Tall, A. R.
Affiliations
  • Columbia University Irving Medical Center (US)
  • University of Bonn (DE)
  • Maastricht University (NL)
  • Department of Pathology Columbia University New York New York USA
Venue
The FASEB Journal
Publisher
Wiley
Published
2007-11-26
Volume
22
Issue
4
Pages
1073-1082
ISSN
  • 0892-6638 (ISSN-L)
  • 1530-6860
OpenAlex
W2093810123
Cited by
184
References
2
Citations by year
2026: 1 · 2025: 6 · 2024: 6 · 2023: 13 · 2022: 12 · 2021: 7 · 2020: 8 · 2019: 6 · 2018: 6 · 2017: 10 · 2016: 9 · 2015: 10 · 2014: 8 · 2013: 12 · 2012: 14
FWCI
13.27
Type
journal article
Language
en
Open access
closed
Locations
  • The FASEB Journal (publishedVersion)
  • PubMed (publishedVersion)
  • Research Publications (Maastricht University) (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
  • Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
Keywords
ABCG1, ABCG4, ABC transporters, cholesterol efflux, desmosterol, HDL cholesterol, astrocytes, cholesterol biosynthesis, lathosterol, lanosterol, 27-hydroxycholesterol, liver X receptor, ABCA1, apolipoprotein E, knockout mice
MeSH terms
ATP Binding Cassette Transporter, Subfamily G, ATP Binding Cassette Transporter, Subfamily G, Member 1, Liver X Receptors, Animals, Apolipoproteins E, Astrocytes, Brain, Cholesterol, Desmosterol, DNA-Binding Proteins, Humans, Lipoproteins, Lipoproteins, HDL, Mice, Transgenic, Receptors, Cytoplasmic and Nuclear, ATP-Binding Cassette Transporters, Mice, Orphan Nuclear Receptors

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