To the top

Page Manager: Webmaster
Last update: 9/11/2012 3:13 PM

Tell a friend about this page
Print version

Amyloid-associated neuron… - University of Gothenburg, Sweden Till startsida
To content Read more about how we use cookies on

Amyloid-associated neuron loss and gliogenesis in the neocortex of amyloid precursor protein transgenic mice.

Journal article
Authors Luca Bondolfi
Michael Calhoun
Florian Ermini
Hans-Georg Kuhn
Karl-Heinz Wiederhold
Lary Walker
Matthias Staufenbiel
Mathias Jucker
Published in The Journal of neuroscience : the official journal of the Society for Neuroscience
Volume 22
Issue 2
Pages 515-22
ISSN 1529-2401
Publication year 2002
Published at
Pages 515-22
Language en
Keywords Aging, metabolism, pathology, Alzheimer Disease, metabolism, pathology, Amyloid beta-Protein Precursor, genetics, Amyloidosis, metabolism, pathology, Animals, Bromodeoxyuridine, Cell Count, Cell Death, Cell Division, Female, Humans, In Situ Nick-End Labeling, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Neocortex, metabolism, pathology, Neuroglia, metabolism, pathology, Neurons, metabolism, pathology, Phenotype
Subject categories Neurosciences


APP23 transgenic mice express mutant human amyloid precursor protein and develop amyloid plaques predominantly in neocortex and hippocampus progressively with age, similar to Alzheimer's disease. We have previously reported neuron loss in the hippocampal CA1 region of 14- to 18-month-old APP23 mice. In contrast, no neuron loss was found in neocortex. In the present study we have reinvestigated neocortical neuron numbers in adult and aged APP23 mice. Surprisingly, results revealed that 8-month-old APP23 mice have 13 and 14% more neocortical neurons compared with 8-month-old wild-type and 27-month-old APP23 mice, respectively. In 27-month-old APP23 mice we found an inverse correlation between amyloid load and neuron number. These results suggest that APP23 mice have more neurons until they develop amyloid plaques but then lose neurons in the process of cerebral amyloidogenesis. Supporting this notion, we found more neurons with a necrotic-apoptotic phenotype in the neocortex of 24-month-old APP23 mice compared with age-matched wild-type mice. Stimulated by recent reports that demonstrated neurogenesis after targeted neuron death in the mouse neocortex, we have also examined neurogenesis in APP23 mice. Strikingly, we found a fourfold to sixfold increase in newly produced cells in 24-month-old APP23 mice compared with both age-matched wild-type mice and young APP23 transgenic mice. However, subsequent cellular phenotyping revealed that none of the newly generated cells in neocortex had a neuronal phenotype. The majority were microglial and to a lesser extent astroglial cells. We conclude that cerebral amyloidosis in APP23 mice causes a modest neuron loss in neocortex and induces marked gliogenesis.

Page Manager: Webmaster|Last update: 9/11/2012

The University of Gothenburg uses cookies to provide you with the best possible user experience. By continuing on this website, you approve of our use of cookies.  What are cookies?

Denna text är utskriven från följande webbsida:
Utskriftsdatum: 2020-02-21