Mamma Mia, P-glycoprotein binds again

FEBS Lett. 2020 Dec;594(23):4076-4084. doi: 10.1002/1873-3468.13951. Epub 2020 Oct 20.

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.

Keywords: ABCB1; Alzheimer’s disease; MDR1; Pgp; amyloid peptides; blood-brain barrier; hydrophobic peptides; membrane transport.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
  • Amyloid beta-Peptides / metabolism*
  • Animals
  • Endothelial Cells
  • Humans
  • Neurons / metabolism*

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Amyloid beta-Peptides