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Adult Neural Stem Cell Migration Is Impaired in a Mouse Model of Alzheimer's Disease

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F22%3A10435047" target="_blank" >RIV/00216208:11130/22:10435047 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378041:_____/22:00580370

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=UXfzvufEQX" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=UXfzvufEQX</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s12035-021-02620-6" target="_blank" >10.1007/s12035-021-02620-6</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Adult Neural Stem Cell Migration Is Impaired in a Mouse Model of Alzheimer's Disease

  • Original language description

    Neurogenesis in the adult brain takes place in two neurogenic niches: the ventricular-subventricular zone (V-SVZ) and the subgranular zone. After differentiation, neural precursor cells (neuroblasts) have to move to an adequate position, a process known as neuronal migration. Some studies show that in Alzheimer&apos;s disease, the adult neurogenesis is impaired. Our main aim was to investigate some proteins involved both in the physiopathology of Alzheimer&apos;s disease and in the neuronal migration process using the APP/PS1 Alzheimer&apos;s mouse model. Progenitor migrating cells are accumulated in the V-SVZ of the APP/PS1 mice. Furthermore, we find an increase of Cdh1 levels and a decrease of Cdk5/p35 and cyclin B1, indicating that these cells have an alteration of the cell cycle, which triggers a senescence state. We find less cells in the rostral migratory stream and less mature neurons in the olfactory bulbs from APP/PS1 mice, leading to an impaired odour discriminatory ability compared with WT mice. Alzheimer&apos;s disease mice present a deficit in cell migration from V-SVZ due to a senescent phenotype. Therefore, these results can contribute to a new approach of Alzheimer&apos;s based on senolytic compounds or pro-neurogenic factors.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30103 - Neurosciences (including psychophysiology)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Molecular Neurobiology

  • ISSN

    0893-7648

  • e-ISSN

    1559-1182

  • Volume of the periodical

    59

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    15

  • Pages from-to

    1168-1182

  • UT code for WoS article

    000729212400001

  • EID of the result in the Scopus database

    2-s2.0-85120917074