In vitro reconstitution demonstrates the amyloid-beta mediated myelin membrane deformation

Abstract

Amyloid-beta (Ab) aggregation mediated neuronal membrane deformation, although poorly understood, is implicated in Alzheimer's Disease (AD). Particularly, whether Ab aggregation can induce neuronal demyelination remains unknown. Here we show that Aβ-40 binds and induces extensive tubulation in the myelin membrane in vitro. The binding of Aβ-40 depends predominantly on the lipid packing defect densities and electrostatic interactions and results in rigidification of the myelin membrane in the early time scales. Furthermore, elongation of Aβ-40 into higher oligomeric and fibrillar species leads to eventual fluidization of the myelin membrane followed by extensive membrane tubulation observed in the late phase. Taken together, our results capture mechanistic insights into snapshots of temporal dynamics of Aβ-40- myelin membrane interaction and demonstrate how short timescale, local phenomena of binding, and fibril mediated load generation manifests into long timescale, global phenomena of myelin tubulation and demonstrates the ability of Aβ-40 to demyelinate.

Mechanical Responses of a Single Myelin Layer: A Molecular Simulation Study

“…Few other studies have focused on the biological aspects of how myelin interacts with other components [13,[34][35][36][37][38][39]. In a recent study, the interaction of myelin basic protein (MBP) in varying concentrations with the plasma membrane was studied using the Langmuir-Blodgett (LB) membrane method with AFM [34].…”