Amyloid β oligomers suppress excitatory transmitter release via presynaptic depletion of phosphatidylinositol-4,5-bisphosphate.

Abstract:

:Amyloid β (Aβ) oligomer-induced aberrant neurotransmitter release is proposed to be a crucial early event leading to synapse dysfunction in Alzheimer's disease (AD). In the present study, we report that the release probability (Pr) at the synapse between the Schaffer collateral (SC) and CA1 pyramidal neurons is significantly reduced at an early stage in mouse models of AD with elevated Aβ production. High nanomolar synthetic oligomeric Aβ42 also suppresses Pr at the SC-CA1 synapse in wild-type mice. This Aβ-induced suppression of Pr is mainly due to an mGluR5-mediated depletion of phosphatidylinositol-4,5-bisphosphate (PIP2) in axons. Selectively inhibiting Aβ-induced PIP2 hydrolysis in the CA3 region of the hippocampus strongly prevents oligomeric Aβ-induced suppression of Pr at the SC-CA1 synapse and rescues synaptic and spatial learning and memory deficits in APP/PS1 mice. These results first reveal the presynaptic mGluR5-PIP2 pathway whereby oligomeric Aβ induces early synaptic deficits in AD.

journal_name

Nat Commun

journal_title

Nature communications

authors

He Y,Wei M,Wu Y,Qin H,Li W,Ma X,Cheng J,Ren J,Shen Y,Chen Z,Sun B,Huang FD,Shen Y,Zhou YD

doi

10.1038/s41467-019-09114-z

subject

Has Abstract

pub_date

2019-03-13 00:00:00

pages

1193

issue

1

issn

2041-1723

pii

10.1038/s41467-019-09114-z

journal_volume

10

pub_type

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