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Localization of cholesterol, amyloid and glia in Alzheimer's disease transgenic mouse brain tissue using time-of-flight secondary ion mass spectrometry (ToF-SIMS) and immunofluorescence imaging

Solé-Domènech, Santiago (author)
Karolinska Institutet
Sjövall, Peter (author)
RISE,SP Kemi Material och Ytor,SP Technical Research Institute Sweden, Sweden,SP – Sveriges Tekniska Forskningsinstitut / Funktionella material (KMf)
Vukojevic, Vladana B. (author)
Karolinska Institutet
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Fernando, Ruani (author)
Institut des Neurosciences de Montpellier, France,Hop St Eloi, France
Codita, Alina (author)
Karolinska Institutet
Salve, Sachin (author)
Karolinska Institutet
Bogdanovic, Nenad E. (author)
Karolinska Institutet
Mohammed, Abdul H. (author)
Karolinska Institutet
Hammarström, Per (author)
Linköpings universitet,Biokemi,Tekniska högskolan
Nilsson, Peter (author)
Linköpings universitet,Kemi,Tekniska fakulteten
Laferla, Frank M. (author)
University of California Irvine, USA,University of Calif Irvine, CA USA
Jacob, Stefan (author)
Karolinska Institute, Sweden
Berggren, Per Olof (author)
Karolinska Institutet
Gimenez-Llort, Lydia (author)
Universitat Autonoma de Barcelona, Spain
Schalling, Martin (author)
Karolinska Institutet
Terenius, Lars H. (author)
Karolinska Institutet
Johansson, Björn (author)
Karolinska Institutet
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 (creator_code:org_t)
2012-09-21
2013
English.
In: Acta Neuropathologica. - : Springer Science and Business Media LLC. - 0001-6322 .- 1432-0533. ; 125:1, s. 145-157
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The spatial distributions of lipids, amyloid-beta deposits, markers of neurons and glial cells were imaged, at submicrometer lateral resolution, in brain structures of a mouse model of Alzheimer's disease using a new methodology that combines time-of-flight secondary ion mass spectrometry (ToF-SIMS) and confocal fluorescence microscopy. The technology, which enabled us to simultaneously image the lipid and glial cell distributions in Tg2576 mouse brain structures, revealed micrometer-sized cholesterol accumulations in hippocampal regions undergoing amyloid-beta deposition. Such cholesterol granules were either associated with individual amyloid deposits or spread over entire regions undergoing amyloidogenesis. Subsequent immunohistochemical analysis of the same brain regions showed increased microglial and astrocytic immunoreactivity associated with the amyloid deposits, as expected from previous studies, but did not reveal any particular astrocytic or microglial feature correlated with cholesterol granulation. However, dystrophic neurites as well as presynaptic vesicles presented a distribution similar to that of cholesterol granules in regions undergoing amyloid-beta accumulation, thus indicating that these neuronal endpoints may retain cholesterol in areas with lesions. In conclusion, the present study provides evidence for an altered cholesterol distribution near amyloid deposits that would have been missed by several other lipid analysis methods, and opens for the possibility to study in detail the putative liaison between lipid environment and protein structure and function in Alzheimer's disease.

Keyword

Alzheimer's disease
Amyloid-beta
Brain
Cholesterol
Glia
Imaging
ToF-SIMS
amyloid beta protein
cell protein
glial fibrillary acidic protein
protein Iba1
unclassified drug
Alzheimer disease
animal experiment
animal model
animal tissue
article
brain level
cellular distribution
confocal laser microscopy
controlled study
glia cell
hippocampus
immunofluorescence
immunohistochemistry
immunoreactivity
lipid analysis
lipid storage
molecular imaging
mouse
nonhuman
priority journal
protein analysis
protein localization
protein structure
scanning electron microscopy
time of flight mass spectrometry
time of flight secondary ion mass spectrometry
Amyloid
Animals
Disease Models
Animal
Fluorescent Antibody Technique
Humans
Mice
Mice
129 Strain
Mice
Inbred C57BL
Mice
Transgenic
Neuroglia
Neurons
Spectrometry
Mass
Secondary Ion
MEDICINE

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ref (subject category)
art (subject category)

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