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Fibrillar amyloid plaque formation precedes microglial activation.
Jung, Christian K E; Keppler, Kevin; Steinbach, Sonja; Blazquez-Llorca, Lidia; Herms, Jochen.
Affiliation
  • Jung CK; Department for Translational Brain Research, German Center for Neurodegenerative Diseases-site Munich (DZNE-M) and Center for Neuropathology and Prion Research (ZNP), Ludwig-Maximilians-University Munich, Munich, Germany.
  • Keppler K; Department for Translational Brain Research, German Center for Neurodegenerative Diseases-site Munich (DZNE-M) and Center for Neuropathology and Prion Research (ZNP), Ludwig-Maximilians-University Munich, Munich, Germany.
  • Steinbach S; Department for Translational Brain Research, German Center for Neurodegenerative Diseases-site Munich (DZNE-M) and Center for Neuropathology and Prion Research (ZNP), Ludwig-Maximilians-University Munich, Munich, Germany.
  • Blazquez-Llorca L; Department for Translational Brain Research, German Center for Neurodegenerative Diseases-site Munich (DZNE-M) and Center for Neuropathology and Prion Research (ZNP), Ludwig-Maximilians-University Munich, Munich, Germany.
  • Herms J; Department for Translational Brain Research, German Center for Neurodegenerative Diseases-site Munich (DZNE-M) and Center for Neuropathology and Prion Research (ZNP), Ludwig-Maximilians-University Munich, Munich, Germany; Munich Cluster of Systems Neurology (SyNergy), Munich, Germany.
PLoS One ; 10(3): e0119768, 2015.
Article in En | MEDLINE | ID: mdl-25799372
ABSTRACT
In Alzheimer's disease (AD), hallmark ß-amyloid deposits are characterized by the presence of activated microglia around them. Despite an extensive characterization of the relation of amyloid plaques with microglia, little is known about the initiation of this interaction. In this study, the detailed investigation of very small plaques in brain slices in AD transgenic mice of the line APP-PS1(dE9) revealed different levels of microglia recruitment. Analysing plaques with a diameter of up to 10 µm we find that only the half are associated with clear morphologically activated microglia. Utilizing in vivo imaging of new appearing amyloid plaques in double-transgenic APP-PS1(dE9)xCX3CR1+/- mice further characterized the dynamic of morphological microglia activation. We observed no correlation of morphological microglia activation and plaque volume or plaque lifetime. Taken together, our results demonstrate a very prominent variation in size as well as in lifetime of new plaques relative to the state of microglia reaction. These observations might question the existing view that amyloid deposits by themselves are sufficient to attract and activate microglia in vivo.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amyloid beta-Protein Precursor / Microglia / Plaque, Amyloid / Receptors, Chemokine / Disease Models, Animal / Presenilin-1 / Alzheimer Disease Type of study: Etiology_studies Limits: Animals / Female / Humans / Male Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2015 Document type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amyloid beta-Protein Precursor / Microglia / Plaque, Amyloid / Receptors, Chemokine / Disease Models, Animal / Presenilin-1 / Alzheimer Disease Type of study: Etiology_studies Limits: Animals / Female / Humans / Male Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2015 Document type: Article Affiliation country: Germany
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