ABCG2- and ABCG4-mediated efflux of amyloid-β peptide 1-40 at the mouse blood-brain barrier - PubMed (original) (raw)
doi: 10.3233/JAD-2012-112189.
Marie-Sophie Noel-Hudson, Sandy Ribes, Capucine Besengez, Maria Smirnova, Salvatore Cisternino, Marion Buyse, Frédéric Calon, Giovanna Chimini, Hélène Chacun, Jean-Michel Scherrmann, Robert Farinotti, Fanchon Bourasset
Affiliations
- PMID: 22391220
- DOI: 10.3233/JAD-2012-112189
ABCG2- and ABCG4-mediated efflux of amyloid-β peptide 1-40 at the mouse blood-brain barrier
Tuan Minh Do et al. J Alzheimers Dis. 2012.
Abstract
The accumulation of amyloid-β peptide (Aβ) in the brain is a critical hallmark of Alzheimer's disease. This high cerebral Aβ concentration may be partly caused by impaired clearance of Aβ across the blood-brain barrier (BBB). The low-density lipoprotein receptor-related protein-1 (LRP-1) and the ATP-binding cassette (ABC) protein ABCB1 (P-glycoprotein) are involved in the efflux of Aβ across the BBB. We hypothesized that other ABC proteins, such as members of the G subfamily, are also involved in the BBB clearance of Aβ. We therefore investigated the roles of ABCG2 (BCRP) and ABCG4 in the efflux of [3H] Aβ1-40 from HEK293 cells stably transfected with human ABCG2 or mouse abcg4. We showed that ABCG2 and Abcg4 mediate the cellular efflux of [3H] Aβ1-40. In addition, probucol fully inhibited the efflux of [3H] Aβ1-40 from HEK293-abcg4 cells. Using the in situ brain perfusion technique, we showed that GF120918 (dual inhibitor of Abcb1 and Abcg2) strongly enhanced the uptake (Clup, μl/g/s) of [3H] Aβ1-40 by the brains of Abcb1-deficient mice, but not by the brains of Abcb1/Abcg2-deficient mice, suggesting that Abcg2 is involved in the transport of Aβ at the mouse BBB. Perfusing the brains of Abcb1/Abcg2- and Abca1-deficient mice with [3H] Aβ1-40 plus probucol significantly increased the Clup of Aβ. This suggests that a probucol-sensitive transporter that is different from Abca1, Abcb1, and Abcg2 is involved in the brain efflux of Aβ. We suggest that this probucol-sensitive transporter is Abcg4. We conclude that Abcg4 acts in concert with Abcg2 to efflux Aβ from the brain across the BBB.
Similar articles
- Age-Dependent Regulation of the Blood-Brain Barrier Influx/Efflux Equilibrium of Amyloid-β Peptide in a Mouse Model of Alzheimer's Disease (3xTg-AD).
Do TM, Dodacki A, Alata W, Calon F, Nicolic S, Scherrmann JM, Farinotti R, Bourasset F. Do TM, et al. J Alzheimers Dis. 2016;49(2):287-300. doi: 10.3233/JAD-150350. J Alzheimers Dis. 2016. PMID: 26484906 - Investigation of efflux transport of dehydroepiandrosterone sulfate and mitoxantrone at the mouse blood-brain barrier: a minor role of breast cancer resistance protein.
Lee YJ, Kusuhara H, Jonker JW, Schinkel AH, Sugiyama Y. Lee YJ, et al. J Pharmacol Exp Ther. 2005 Jan;312(1):44-52. doi: 10.1124/jpet.104.073320. Epub 2004 Sep 24. J Pharmacol Exp Ther. 2005. PMID: 15448171 - Therapeutic drugs modulate ATP-Binding cassette transporter-mediated transport of amyloid beta(1-42) in brain microvascular endothelial cells.
Shubbar MH, Penny JI. Shubbar MH, et al. Eur J Pharmacol. 2020 May 5;874:173009. doi: 10.1016/j.ejphar.2020.173009. Epub 2020 Feb 13. Eur J Pharmacol. 2020. PMID: 32061744 - Role of ABC transporters in the pathogenesis of Alzheimer's disease.
Abuznait AH, Kaddoumi A. Abuznait AH, et al. ACS Chem Neurosci. 2012 Nov 21;3(11):820-31. doi: 10.1021/cn300077c. Epub 2012 Oct 11. ACS Chem Neurosci. 2012. PMID: 23181169 Free PMC article. Review. - Human ABC transporters ABCG2 (BCRP) and ABCG4.
Koshiba S, An R, Saito H, Wakabayashi K, Tamura A, Ishikawa T. Koshiba S, et al. Xenobiotica. 2008 Jul;38(7-8):863-88. doi: 10.1080/00498250801986944. Xenobiotica. 2008. PMID: 18668433 Review.
Cited by
- Functional Cooperativity between ABCG4 and ABCG1 Isoforms.
Hegyi Z, Homolya L. Hegyi Z, et al. PLoS One. 2016 May 26;11(5):e0156516. doi: 10.1371/journal.pone.0156516. eCollection 2016. PLoS One. 2016. PMID: 27228027 Free PMC article. - Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer's disease?
Estudillo E, López-Ornelas A, Rodríguez-Oviedo A, Gutiérrez de la Cruz N, Vargas-Hernández MA, Jiménez A. Estudillo E, et al. Neural Regen Res. 2023 Dec;18(12):2592-2598. doi: 10.4103/1673-5374.373672. Neural Regen Res. 2023. PMID: 37449594 Free PMC article. Review. - Strategies to gain novel Alzheimer's disease diagnostics and therapeutics using modulators of ABCA transporters.
Pahnke J, Bascuñana P, Brackhan M, Stefan K, Namasivayam V, Koldamova R, Wu J, Möhle L, Stefan SM. Pahnke J, et al. Free Neuropathol. 2021;2:2-33. doi: 10.17879/freeneuropathology-2021-3528. Epub 2021 Dec 13. Free Neuropathol. 2021. PMID: 34977908 Free PMC article. - Impact of Coffee and Cacao Purine Metabolites on Neuroplasticity and Neurodegenerative Disease.
Camandola S, Plick N, Mattson MP. Camandola S, et al. Neurochem Res. 2019 Jan;44(1):214-227. doi: 10.1007/s11064-018-2492-0. Epub 2018 Feb 8. Neurochem Res. 2019. PMID: 29417473 Free PMC article. Review. - New Evidence for P-gp-Mediated Export of Amyloid-β PEPTIDES in Molecular, Blood-Brain Barrier and Neuronal Models.
Chai AB, Hartz AMS, Gao X, Yang A, Callaghan R, Gelissen IC. Chai AB, et al. Int J Mol Sci. 2020 Dec 29;22(1):246. doi: 10.3390/ijms22010246. Int J Mol Sci. 2020. PMID: 33383667 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous