Literature DB >> 27343974

The Tyr216 phosphorylated form of GSK3β contributes to tau phosphorylation at PHF-1 epitope in response to Aβ in the nucleus of SH-SY5Y cells.

Anastasia Noel1, Laurence Barrier2, Sabrina Ingrand3.   

Abstract

AIMS: GSK3β activation in Aβ conditions leading to tau phosphorylation at pathological sites is a well-known phenomenon. However, the serine/tyrosine phosphorylation processes implied in Aβ-induced GSK3β activation and responsible for tau phosphorylation, especially at the GSK3β specific Ser396/Ser404 (PHF-1) site, are still debated. MAIN
METHODS: Experiments were performed on SH-SY5Y cells exposed to 20μM Aβ1-42 in a time ranging from 5min to 8h. The phophorylated forms (Ser9 and Tyr216) of GSK3β and pTau at PHF-1 epitope were measured by immunoblotting in nuclear extracts. KEY
FINDINGS: We showed a superimposable time-dependent increase of nuclear pGSK3βTyr216 and nuclear pTau at PHF-1 site, both reaching their maximal level after 8h of Aβ1-42 exposure. In addition, nuclear accumulation of pTau is accompanied by its cytoplasmic decrease suggesting that pTau is translocated in response to Aβ treatment. Besides, our experiments showed that specific pGSK3βTyr216 inhibition is required to drop nuclear pTau, ensuring the involvement of Tyr216 phosphorylation in Aβ-mediated tau phosphorylation at PHF-1 epitope. SIGNIFICANCE: These data suggested that in response to Aβ exposure in SH-SY5Y cells, GSK3β activation is performed through Tyr216 phosphorylation and resulted in tau phosphorylation at PHF-1 epitope and in its translocation.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Abeta; Glycogen synthase kinase-3 beta; PHF-1 epitope; SH-SY5Y cell lines; Tau phosphorylation; Tyrosine216 phosphorylation

Mesh:

Substances:

Year:  2016        PMID: 27343974     DOI: 10.1016/j.lfs.2016.06.020

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  6 in total

1.  Increased Tau Phosphorylation in Motor Neurons From Clinically Pure Sporadic Amyotrophic Lateral Sclerosis Patients.

Authors:  Claire H Stevens; Natalie J Guthrie; Marloes van Roijen; Glenda M Halliday; Lezanne Ooi
Journal:  J Neuropathol Exp Neurol       Date:  2019-07-01       Impact factor: 3.685

2.  The Involvement of Aβ42 and Tau in Nucleolar and Protein Synthesis Machinery Dysfunction.

Authors:  Mahmoud B Maina; Laura J Bailey; Aidan J Doherty; Louise C Serpell
Journal:  Front Cell Neurosci       Date:  2018-08-03       Impact factor: 5.505

3.  The involvement of tau in nucleolar transcription and the stress response.

Authors:  Mahmoud B Maina; Laura J Bailey; Sherin Wagih; Luca Biasetti; Saskia J Pollack; James P Quinn; Julian R Thorpe; Aidan J Doherty; Louise C Serpell
Journal:  Acta Neuropathol Commun       Date:  2018-07-31       Impact factor: 7.801

4.  IGF1R Deficiency Modulates Brain Signaling Pathways and Disturbs Mitochondria and Redox Homeostasis.

Authors:  Susana Cardoso; Icíar P López; Sergio Piñeiro-Hermida; José G Pichel; Paula I Moreira
Journal:  Biomedicines       Date:  2021-02-06

5.  miR-200c suppression increases tau hyperphosphorylation by targeting 14-3-3γ in early stage of 5xFAD mouse model of Alzheimer's disease.

Authors:  Hyunjun Park; Yeong-Bae Lee; Keun-A Chang
Journal:  Int J Biol Sci       Date:  2022-03-06       Impact factor: 6.580

6.  Galectin-3 Secreted by Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells Reduces Aberrant Tau Phosphorylation in an Alzheimer Disease Model.

Authors:  Hoon Lim; Dahm Lee; Wan Kyu Choi; Soo Jin Choi; Wonil Oh; Dong Hyun Kim
Journal:  Stem Cells Int       Date:  2020-07-18       Impact factor: 5.443

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.