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Deposition of C-terminally truncated A beta species A beta 37 and A beta 39 in Alzheimer's disease and transgenic mouse models

Reinert, Jochim (författare)
Richard, Bernhard C. (författare)
Klafki, Hans W. (författare)
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Friedrich, Beate (författare)
Bayer, Thomas A. (författare)
Wiltfang, Jens (författare)
Kovacs, Gabor G. (författare)
Ingelsson, Martin, 1965- (författare)
Lannfelt, Lars (författare)
Paetau, Anders (författare)
Bergquist, Jonas (författare)
Wirths, Oliver (författare)
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2016
2016
Engelska.
Ingår i: Acta neuropathologica communications. - 1509-409X. ; 4
  • swepub:Mat__t
Abstract Ämnesord
Stäng  
  • In Alzheimer's disease (AD) a variety of amyloid beta-peptides (A beta) are deposited in the form of extracellular diffuse and neuritic plaques (NP), as well as within the vasculature. The generation of A beta from its precursor, the amyloid precursor protein (APP), is a highly complex procedure that involves subsequent proteolysis of APP by beta-and gamma-secretases. Brain accumulation of A beta due to impaired A beta degradation and/or altered ratios between the different A beta species produced is believed to play a pivotal role in AD pathogenesis. While the presence of A beta 40 and A beta 42 in vascular and parenchymal amyloid have been subject of extensive studies, the deposition of carboxyterminal truncated A beta peptides in AD has not received comparable attention. In the current study, we for the first time demonstrate the immunohistochemical localization of A beta 37 and A beta 39 in human sporadic AD (SAD). Our study further included the analysis of familial AD (FAD) cases carrying the APP mutations KM670/671NL, E693G and I716F, as well as a case of the PSEN1 Delta Exon9 mutation. A beta 37 and A beta 39 were found to be widely distributed within the vasculature in the brains of the majority of studied SAD and FAD cases, the latter also presenting considerable amounts of A beta 37 containing NPs. In addition, both peptides were found to be present in extracellular plaques but only scarce within the vasculature in brains of a variety of transgenic AD mouse models. Taken together, our study indicates the importance of C-terminally truncated A beta in sporadic and familial AD and raises questions about how these species are generated and regulated.

Ämnesord

Medical and Health Sciences  (hsv)
Clinical Medicine  (hsv)
Neurology  (hsv)
Medicin och hälsovetenskap  (hsv)
Klinisk medicin  (hsv)
Neurologi  (hsv)

Nyckelord

Alzheimer
C-terminal truncation
Amyloid precursor protein
Transgenic mice
A beta 37
A beta 39
Immunohistochemistry
Mass spectrometry

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