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Amyloid precursor protein expression and processing are differentially regulated during cortical neuron differentiation

Authors :
Petra Bergström
Lotta Agholme
Faisal Hayat Nazir
Tugce Munise Satir
Jamie Toombs
Henrietta Wellington
Joakim Strandberg
Thomas Olsson Bontell
Hlin Kvartsberg
Maria Holmström
Cecilia Boreström
Stina Simonsson
Tilo Kunath
Anders Lindahl
Kaj Blennow
Eric Hanse
Erik Portelius
Selina Wray
Henrik Zetterberg
Source :
Scientific Reports, Bergström, P, Agholme, L, Nazir, F H, Satir, T M, Toombs, J, Wellington, H, Strandberg, J, Bontell, T O, Kvartsberg, H, Holmström, M, Boreström, C, Simonsson, S, Kunath, T, Lindahl, A, Blennow, K, Hanse, E, Portelius, E, Wray, S & Zetterberg, H 2016, ' Amyloid precursor protein expression and processing are differentially regulated during cortical neuron differentiation ', Scientific Reports, vol. 6, 29200 . https://doi.org/10.1038/srep29200
Publication Year :
2016

Abstract

Amyloid precursor protein (APP) and its cleavage product amyloid β (Aβ) have been thoroughly studied in Alzheimer's disease. However, APP also appears to be important for neuronal development. Differentiation of induced pluripotent stem cells (iPSCs) towards cortical neurons enables in vitro mechanistic studies on human neuronal development. Here, we investigated expression and proteolytic processing of APP during differentiation of human iPSCs towards cortical neurons over a 100-day period. APP expression remained stable during neuronal differentiation, whereas APP processing changed. α-Cleaved soluble APP (sAPPα) was secreted early during differentiation, from neuronal progenitors, while β-cleaved soluble APP (sAPPβ) was first secreted after deep-layer neurons had formed. Short Aβ peptides, including Aβ1-15/16, peaked during the progenitor stage, while processing shifted towards longer peptides, such as Aβ1-40/42, when post-mitotic neurons appeared. This indicates that APP processing is regulated throughout differentiation of cortical neurons and that amyloidogenic APP processing, as reflected by Aβ1-40/42, is associated with mature neuronal phenotypes.

Details

ISSN :
20452322
Volume :
6
Database :
OpenAIRE
Journal :
Scientific reports
Accession number :
edsair.pmid.dedup....8a88b04309fd7ffbed4009361cc969e1
Full Text :
https://doi.org/10.1038/srep29200