Literature DB >> 25810511

Tau phosphorylation at serine 396 residue is required for hippocampal LTD.

Philip Regan1, Thomas Piers2, Jee-Hyun Yi3, Dong-Hyun Kim3, Seonghoo Huh4, Se Jin Park5, Jong Hoon Ryu5, Daniel J Whitcomb2, Kwangwook Cho6.   

Abstract

Tau is required for the induction of long-term depression (LTD) of synaptic transmission in the hippocampus. Here we probe the role of tau in LTD, finding that an AMPA receptor internalization mechanism is impaired in tau KO mice, and that LTD causes specific phosphorylation at the serine 396 and 404 residues of tau. Surprisingly, we find that phosphorylation at serine 396, specifically, is critical for LTD but has no role in LTP. Finally, we show that tau KO mice exhibit deficits in spatial reversal learning. These findings underscore the physiological role for tau at the synapse and identify a behavioral correlate of its role in LTD.
Copyright © 2015 the authors 0270-6474/15/354804-09$15.00/0.

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Keywords:  LTD; hippocampus; synaptic plasticity

Mesh:

Substances:

Year:  2015        PMID: 25810511      PMCID: PMC4389589          DOI: 10.1523/JNEUROSCI.2842-14.2015

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  57 in total

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Authors:  Tong Li; Hemant K Paudel
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Review 4.  The complexity of tau in Alzheimer's disease.

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8.  AD-Related N-Terminal Truncated Tau Is Sufficient to Recapitulate In Vivo the Early Perturbations of Human Neuropathology: Implications for Immunotherapy.

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Review 9.  Interactions Between α-Synuclein and Tau Protein: Implications to Neurodegenerative Disorders.

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Review 10.  Molecular and cellular mechanisms underlying the pathogenesis of Alzheimer's disease.

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