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Sökning: id:"swepub:oai:DiVA.org:uu-282802" > Deposition of C-ter...

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)
Univ Gottingen, Univ Med Ctr UMG, Div Mol Psychiat, D-37075 Gottingen, Germany.
Richard, Bernhard C. (författare)
Univ Gottingen, Univ Med Ctr UMG, Div Mol Psychiat, D-37075 Gottingen, Germany.
Klafki, Hans W. (författare)
Univ Gottingen, Univ Med Ctr UMG, Dept Psychiat & Psychotherapy, Von Siebold Str 5, D-37075 Gottingen, Germany.
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Friedrich, Beate (författare)
Synapt Syst, Gottingen, Germany.
Bayer, Thomas A. (författare)
Univ Gottingen, Univ Med Ctr UMG, Div Mol Psychiat, D-37075 Gottingen, Germany.;Univ Gottingen, Univ Med Ctr UMG, Dept Psychiat & Psychotherapy, Von Siebold Str 5, D-37075 Gottingen, Germany.
Wiltfang, Jens (författare)
Univ Gottingen, Univ Med Ctr UMG, Dept Psychiat & Psychotherapy, Von Siebold Str 5, D-37075 Gottingen, Germany.
Kovacs, Gabor G. (författare)
Med Univ Vienna, Inst Neurol, Vienna, Austria.
Ingelsson, Martin (författare)
Uppsala universitet,Geriatrik
Lannfelt, Lars (författare)
Uppsala universitet,Geriatrik
Paetau, Anders (författare)
Univ Helsinki, Dept Pathol, Helsinki, Finland.;Univ Helsinki Hosp, Helsinki, Finland.
Bergquist, Jonas (författare)
Uppsala universitet,Analytisk kemi,Science for Life Laboratory, SciLifeLab
Wirths, Oliver (författare)
Univ Gottingen, Univ Med Ctr UMG, Div Mol Psychiat, D-37075 Gottingen, Germany.;Univ Gottingen, Univ Med Ctr UMG, Dept Psychiat & Psychotherapy, Von Siebold Str 5, D-37075 Gottingen, Germany.
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Univ Gottingen, Univ Med Ctr UMG, Div Mol Psychiat, D-37075 Gottingen, Germany Univ Gottingen, Univ Med Ctr UMG, Dept Psychiat & Psychotherapy, Von Siebold Str 5, D-37075 Gottingen, Germany. (creator_code:org_t)
2016-03-08
2016
Engelska.
Ingår i: Acta neuropathologica communications. - : Springer Science and Business Media LLC. - 2051-5960. ; 4
  • Tidskriftsartikel (refereegranskat)
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

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

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

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