ATP‐binding cassette transporters G1 and G4 mediate cholesterol and desmosterol efflux to HDL and regulate sterol accumulation in the brain
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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Desmosterol accumulation could be regarded as an attempt to activate LXR signaling and thereby increase sterol secretion from astrocytes.
“Desmosterol accumulation could also be regarded as an attempt to activate LXR signaling and thereby increase sterol secretion from astrocytes32,33.”
From An iPSC-derived astrocyte model of fragile X syndrome exhibits dysregulated cholesterol homeostasis (2023) · cites this paper as [32]
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Secretion of Sterols and the NPC2 Protein from Primary Astrocytes
Mutka, A.-L., Lusa, S., Linder, M. D., Jokitalo, E., Kopra, O., Jauhiainen, M., & Ikonen, E. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m405345200 · Cited by 56 · see citing works
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Central Nervous System Lipoproteins: ApoE and Regulation of Cholesterol Metabolism
Mahley, R. W. (2016) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.116.307023 · Cited by 516 · see citing works
Cholesterol metabolism in neurons and astrocytes
Pfrieger, F. W., & Ungerer, N. (2011) · Progress in Lipid Research · doi:10.1016/j.plipres.2011.06.002 · Cited by 500 · see citing works
Mazur, M. T., Cardasis, H. L., Spellman, D. S., Liaw, A., Yates, N. A., & Hendrickson, R. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910776107 · Cited by 87 · see citing works
What dictates the accumulation of desmosterol in the developing brain?
Jansen, M., Wang, W., Greco, D., Bellenchi, G. C., di Porzio, U., Brown, A. J., & Ikonen, E. (2013) · The FASEB Journal · doi:10.1096/fj.12-211235 · Cited by 42 · see citing works
Peroxisomal defects in microglial cells induce a disease-associated microglial signature
Raas, Q., Tawbeh, A., Tahri-Joutey, M., Gondcaille, C., Keime, C., Kaiser, R., Trompier, D., Nasser, B., Leoni, V., Bellanger, E., et al. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1170313 · Cited by 16 · see citing works
An iPSC-derived astrocyte model of fragile X syndrome exhibits dysregulated cholesterol homeostasis
Talvio, K., Wagner, V. A., Minkeviciene, R., Kirkwood, J. S., Kulinich, A. O., Umemori, J., Bhatia, A., Hur, M., Käkelä, R., Ethell, I. M., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-05147-9 · Cited by 8 · see citing works
- 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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