1. Academic Validation
  2. Age-dependent changes in synaptic plasticity enhance tau oligomerization in the mouse hippocampus

Age-dependent changes in synaptic plasticity enhance tau oligomerization in the mouse hippocampus

  • Acta Neuropathol Commun. 2017 Sep 6;5(1):67. doi: 10.1186/s40478-017-0469-x.
Tetsuya Kimura 1 2 Mamiko Suzuki 3 Takumi Akagi 4
Affiliations

Affiliations

  • 1 Department of Aging Neurobiology, Center for Development for Advanced Medicine for Dementia, National Center for Geriatrics and Gerontology, 7-430 Omori-cho, Obu-shi, Aichi, 474-8511, Japan. kimura_t@ncgg.go.jp.
  • 2 Present Address: Department of Alzheimer's Disease Research, Center for Development for Advanced Medicine for Dementia, National Center for Geriatrics and Gerontology, 7-430 Omori-cho, Obu-shi, Aichi, 474-8511, Japan. kimura_t@ncgg.go.jp.
  • 3 Department of Aging Neurobiology, Center for Development for Advanced Medicine for Dementia, National Center for Geriatrics and Gerontology, 7-430 Omori-cho, Obu-shi, Aichi, 474-8511, Japan.
  • 4 Support Unit for Animal Resources Development, Research Resources Center, Brain Science Institute, RIKEN, Wako, Saitama, 351-0198, Japan.
Abstract

The aggregation mechanism of phosphorylated tau is an important therapeutic target for tauopathies, including Alzheimer's disease, although the mechanism by which aggregation occurs is still unknown. Because the phosphorylation process of tau is involved in the trafficking of AMPA receptors, which accompanies the long-term depression (LTD) of synapses, we examined the effect of LTD-inducing low-frequency stimulation (LFS) on the formation of pathological tau aggregates in adult and aged wild-type mice. Our biochemical analysis demonstrated that LFS led to the formation of sarkosyl-insoluble (SI) tau oligomers in aged hippocampi but not in adult hippocampi in wild-type mice. In parallel, electrophysiological experiments showed an increased contribution of the autophagy-lysosomal pathway (ALP) to LTD during aging, although the other properties of LFS-induced LTD that we investigated were not altered. Thus, we anticipate that the increased contribution of the ALP to the LTD cascade is involved in the age-dependent formation of tau oligomers that results from LFS. Analysis of the LC3 ratio, an indicator of autophagosome formation, showed that LFS increased cleaved LC3 (type II) in the aged hippocampus relative to type I LC3, suggesting potentiation of the ALP accompanied by LTD. Pharmacological inhibition of autophagosome formation depressed LFS-induced oligomerization of tau. Prevention of lysosomal function in the ALP enhanced the formation of tau oligomers by LFS. These results suggest the importance of the autophagosome for the LFS-induced oligomerization of tau and suggest a reason for its age dependency. Interestingly, the lysosomal disturbance promoted the formation of the fibrillar form of aggregates consisting of hyper-phosphorylated tau. The LTD-ALP cascade potentially acts as one of the suppliers of pathological aggregates of tau in aged neurons.

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