Plasmalogens Inhibit APP Processing by Directly Affectingγ-Secretase Activity in Alzheimer’s Disease

Author:

Rothhaar Tatjana L.1,Grösgen Sven1,Haupenthal Viola J.1,Burg Verena K.1,Hundsdörfer Benjamin1,Mett Janine1,Riemenschneider Matthias2,Grimm Heike S.1,Hartmann Tobias134,Grimm Marcus O. W.134

Affiliation:

1. Experimental Neurology, Saarland University, Kirrbergerstraβe, 66421 Homburg/Saar, Germany

2. Psychiatry, Saarland University, Kirrbergerstraβe, 66421 Homburg/Saar, Germany

3. Deutsches Institut für DemenzPrävention (DIDP), Universität des Saarlandes, Kirrbergerstraβe, 66421 Homburg/Saar, Germany

4. Neurodegeneration and Neurobiology, Saarland University, Kirrbergerstraβe, 66421 Homburg/Saar, Germany

Abstract

Lipids play an important role as risk or protective factors in Alzheimer’s disease (AD). Previously it has been shown that plasmalogens, the major brain phospholipids, are altered in AD. However, it remained unclear whether plasmalogens themselves are able to modulate amyloid precursor protein (APP) processing or if the reduced plasmalogen level is a consequence of AD. Here we identify the plasmalogens which are altered in human ADpostmortembrains and investigate their impact on APP processing resulting in Aβ production. All tested plasmalogen species showed a reduction in γ-secretase activity whereas β- and α-secretase activity mainly remained unchanged. Plasmalogens directly affected γ-secretase activity, protein and RNA level of the secretases were unaffected, pointing towards a direct influence of plasmalogens on γ-secretase activity. Plasmalogens were also able to decrease γ-secretase activity in humanpostmortemAD brains emphasizing the impact of plasmalogens in AD. In summary our findings show that decreased plasmalogen levels are not only a consequence of AD but that plasmalogens also decrease APP processing by directly affecting γ-secretase activity, resulting in a vicious cycle: Aβ reduces plasmalogen levels and reduced plasmalogen levels directly increase γ-secretase activity leading to an even stronger production of Aβ peptides.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Hindawi Limited

Subject

General Environmental Science,General Biochemistry, Genetics and Molecular Biology,General Medicine

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