Mapping synaptic glutamate transporter dysfunction in vivo to regions surrounding A? plaques by iGluSnFR two-photon imaging.

ABSTRACT: Amyloid-? (A?) plaques, a hallmark of Alzheimer's disease (AD), are surrounded by regions of neuronal and glial hyperactivity. We use in vivo two-photon and wide-field imaging of the glutamate sensor iGluSnFR to determine whether pathological changes in glutamate dynamics in the immediate vicinity of A? deposits in APPPS1 transgenic mice could alter neuronal activity in this microenvironment. In regions close to A? plaques chronic states of high spontaneous glutamate fluctuations are observed and the timing of glutamate responses evoked by sensory stimulation exhibit slower decay rates in two cortical brain areas. GLT-1 expression is reduced around A? plaques and upregulation of GLT-1 expression and activity by ceftriaxone partially restores glutamate dynamics to values in control regions. We conclude that the toxic microenvironment surrounding A? plaques results, at least partially, from enhanced glutamate levels and that pharmacologically increasing GLT-1 expression and activity may be a new target for early therapeutic intervention.

SUBMITTER: Hefendehl JK 

PROVIDER: S-EPMC5114608 | biostudies-literature | 2016 Nov

REPOSITORIES: biostudies-literature