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Publication : Dysfunction of the glutamatergic photoreceptor synapse in the P301S mouse model of tauopathy.

First Author  Arouche-Delaperche L Year  2023
Journal  Acta Neuropathol Commun Volume  11
Issue  1 Pages  5
PubMed ID  36631898 Mgi Jnum  J:332525
Mgi Id  MGI:7426130 Doi  10.1186/s40478-022-01489-3
Citation  Arouche-Delaperche L, et al. (2023) Dysfunction of the glutamatergic photoreceptor synapse in the P301S mouse model of tauopathy. Acta Neuropathol Commun 11(1):5
abstractText  Tauopathies, including Alzheimer's disease, are characterized by retinal ganglion cell loss associated with amyloid and phosphorylated tau deposits. We investigated the functional impact of these histopathological alterations in the murine P301S model of tauopathy. Visual impairments were demonstrated by a decrease in visual acuity already detectable at 6 months, the onset of disease. Visual signals to the cortex and retina were delayed at 6 and 9 months, respectively. Surprisingly, the retinal output signal was delayed at the light onset and advanced at the light offset. This antagonistic effect, due to a dysfunction of the cone photoreceptor synapse, was associated with changes in the expression of the vesicular glutamate transporter and a microglial reaction. This dysfunction of retinal glutamatergic synapses suggests a novel interpretation for visual deficits in tauopathies and it highlights the potential value of the retina for the diagnostic assessment and the evaluation of therapies in Alzheimer's disease and other tauopathies.
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