| Literature DB >> 33022784 |
Richard Callaghan1, Ingrid C Gelissen2, Anthony M George3, Anika M S Hartz4.
Abstract
The levels of amyloid peptides in the brain are regulated by a clearance pathway from neurons to the blood-brain barrier. The first step is thought to involve diffusion from the plasma membrane to the interstitium. However, amyloid peptides are hydrophobic and avidly intercalate within membranes. The ABC transporter P-glycoprotein is implicated in the clearance of amyloid peptides across the blood-brain, but its role at neurons is undetermined. We here propose that P-glycoprotein mediates 'exit' of amyloid peptides from neurons. Indeed, amyloid peptides have physicochemical similarities to substrates of P-glycoprotein, but their larger size represents a conundrum. This review probes the plausibility of a mechanism for amyloid peptide transport by P-glycoprotein exploiting evolving biochemical and structural models.Entities:
Keywords: ABCB1; Alzheimer’s disease; MDR1; Pgp; amyloid peptides; blood-brain barrier; hydrophobic peptides; membrane transport
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Year: 2020 PMID: 33022784 PMCID: PMC8731231 DOI: 10.1002/1873-3468.13951
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124