z-logo
open-access-imgOpen Access
Progression of Seed‐Induced A β Deposition within the Limbic Connectome
Author(s) -
Ye Lan,
Hamaguchi Tsuyoshi,
Fritschi Sarah K.,
Eisele Yvonne S.,
Obermüller Ulrike,
Jucker Mathias,
Walker Lary C.
Publication year - 2015
Publication title -
brain pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.986
H-Index - 132
eISSN - 1750-3639
pISSN - 1015-6305
DOI - 10.1111/bpa.12252
Subject(s) - hippocampal formation , neuroscience , genetically modified mouse , connectome , pathogenesis , hippocampus , extracellular , amyloid precursor protein , biology , transgene , microbiology and biotechnology , pathology , medicine , disease , alzheimer's disease , immunology , biochemistry , functional connectivity , gene
An important early event in the pathogenesis of A lzheimer's disease ( AD ) is the aberrant polymerization and extracellular accumulation of amyloid‐β peptide ( A β). In young transgenic mice expressing the human A β‐precursor protein ( APP ), deposits of A β can be induced by the inoculation of minute amounts of brain extract containing A β aggregates (“ A β seeds”), indicative of a prion‐like seeding phenomenon. Moreover, focal intracerebral injection of A β seeds can induce deposits not only in the immediate vicinity of the injection site, but, with time, also in distal regions of the brain. However, it remains uncertain whether the spatial progression of A β deposits occurs via nonsystematic diffusion from the injection site to proximal regions or via directed transit along neuroanatomical pathways. To address this question, we analyzed the spatiotemporal emergence of A β deposits in two different APP ‐transgenic mouse models that had been previously inoculated with A β seeds into the hippocampal formation. The results revealed a specific, neuroanatomically constrained pattern of induced A β deposits in structures corresponding to the limbic connectome, supporting the hypothesis that neuronal pathways act as conduits for the movement of proteopathic agents among brain regions, thereby facilitating the progression of disease.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here