NGF controls APP cleavage by downregulating APP phosphorylation at Thr668

Relevance for Alzheimer's disease

Viviana Triaca, Valentina Sposato, Giulia Bolasco, Maria teresa Ciotti, Piergiuseppe Pelicci, Amalia C. Bruni, Chiara Cupidi, Raffaele Maletta, Marco Feligioni, Robert Nisticò, Nadia Canu, Pietro Calissano

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

NGF has been implicated in forebrain neuroprotection from amyloidogenesis and Alzheimer's disease (AD). However, the underlying molecular mechanisms are still poorly understood. Here, we investigated the role of NGF signalling in the metabolism of amyloid precursor protein (APP) in forebrain neurons using primary cultures of septal neurons and acute septo-hippocampal brain slices. In this study, we show that NGF controls the basal level of APP phosphorylation at Thr668 (T668) by downregulating the activity of the Ser/Thr kinase JNK(p54) through the Tyr kinase signalling adaptor SH2-containing sequence C (ShcC). We also found that the specific NGF receptor, Tyr kinase A (TrkA), which is known to bind to APP, fails to interact with the fraction of APP molecules phosphorylated at T668 (APPpT668). Accordingly, the amount of TrkA bound to APP is significantly reduced in the hippocampus of ShcC KO mice and of patients with AD in which elevated APPpT668 levels are detected. NGF promotes TrkA binding to APP and APP trafficking to the Golgi, where APP-BACE interaction is hindered, finally resulting in reduced generation of sAPPβ, CTFβ and amyloid-beta (1-42). These results demonstrate that NGF signalling directly controls basal APP phosphorylation, subcellular localization and BACE cleavage, and pave the way for novel approaches specifically targeting ShcC signalling and/or the APP-TrkA interaction in AD therapy. Copyright

Original languageEnglish
JournalAging Cell
DOIs
Publication statusAccepted/In press - 2016

Fingerprint

Amyloid beta-Protein Precursor
Nerve Growth Factor
Alzheimer Disease
Down-Regulation
Phosphorylation
Phosphotransferases
Prosencephalon
MAP Kinase Kinase 4
Neurons
Nerve Growth Factor Receptor
Protein Transport
Amyloid
Protein Kinases
Hippocampus
Brain

Keywords

  • APP
  • BACE
  • NGF
  • AD
  • ShcC
  • TrkA-APP interaction

ASJC Scopus subject areas

  • Cell Biology
  • Ageing

Cite this

Triaca, V., Sposato, V., Bolasco, G., Ciotti, M. T., Pelicci, P., Bruni, A. C., ... Calissano, P. (Accepted/In press). NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: Relevance for Alzheimer's disease. Aging Cell. https://doi.org/10.1111/acel.12473

NGF controls APP cleavage by downregulating APP phosphorylation at Thr668 : Relevance for Alzheimer's disease. / Triaca, Viviana; Sposato, Valentina; Bolasco, Giulia; Ciotti, Maria teresa; Pelicci, Piergiuseppe; Bruni, Amalia C.; Cupidi, Chiara; Maletta, Raffaele; Feligioni, Marco; Nisticò, Robert; Canu, Nadia; Calissano, Pietro.

In: Aging Cell, 2016.

Research output: Contribution to journalArticle

Triaca, V, Sposato, V, Bolasco, G, Ciotti, MT, Pelicci, P, Bruni, AC, Cupidi, C, Maletta, R, Feligioni, M, Nisticò, R, Canu, N & Calissano, P 2016, 'NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: Relevance for Alzheimer's disease', Aging Cell. https://doi.org/10.1111/acel.12473
Triaca, Viviana ; Sposato, Valentina ; Bolasco, Giulia ; Ciotti, Maria teresa ; Pelicci, Piergiuseppe ; Bruni, Amalia C. ; Cupidi, Chiara ; Maletta, Raffaele ; Feligioni, Marco ; Nisticò, Robert ; Canu, Nadia ; Calissano, Pietro. / NGF controls APP cleavage by downregulating APP phosphorylation at Thr668 : Relevance for Alzheimer's disease. In: Aging Cell. 2016.
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