Evidence map›Paper›PMID 34894324›Full record

ArticleMolecular neurobiology2022

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

Daniel Esteve, María Micaela Molina-Navarro, Esther Giraldo, Noelia Martínez-Varea, Mari-Carmen Blanco-Gandia, Marta Rodríguez-Arias, José Manuel García-Verdugo, José Viña, Ana Lloret

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Daniel EsteveFreshage Research Group, Department of Physiology, Faculty of Medicine, University of Valencia, Valencia, Spain.
María Micaela Molina-NavarroLaboratory of Comparative Neurobiology, Instituto Cavanilles de Biodiversidad Y Biologia Evolutiva, University of Valencia, CIBERNED, Paterna, Valencia, Spain.
Esther GiraldoNeuronal and Tissue Regeneration Laboratory, Centro de Investigación Príncipe Felipe, Valencia, Spain.
Noelia Martínez-VareaInstitute of Experimental Medicine, Czech Academy of Sciences, Prague, Czech Republic.
Mari-Carmen Blanco-GandiaDepartment of Psychobiology, Faculty of Psycology, University of Valencia, Valencia, Spain.
Marta Rodríguez-AriasDepartment of Psychobiology, Faculty of Psycology, University of Valencia, Valencia, Spain.
José Manuel García-VerdugoLaboratory of Comparative Neurobiology, Instituto Cavanilles de Biodiversidad Y Biologia Evolutiva, University of Valencia, CIBERNED, Paterna, Valencia, Spain.
José ViñaFreshage Research Group, Department of Physiology, Faculty of Medicine, University of Valencia, Valencia, Spain. jose.vina@uv.es.
Ana LloretFreshage Research Group, Department of Physiology, Faculty of Medicine, University of Valencia, Valencia, Spain. ana.lloret@uv.es.ORCID http://orcid.org/0000-0003-0266-0304
Universitat de València · ESParc Científic de la Universitat de València · ESCentro de Investigacion Principe Felipe · ESCharles University · CZ

Funding

conselleria de sanitat universal i salut pública PROMETEO/2019/097horizon 2020 696295instituto de salud carlos iii CB16/10/00435joint programming initiative a healthy diet for a healthy life 825546ministerio de ciencia, innovación y universidades PID2019-110906RB-I00Universitat de València UV-INV-AE-1546096
6 · The paper itself

Abstract

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's disease, the adult neurogenesis is impaired. Our main aim was to investigate some proteins involved both in the physiopathology of Alzheimer's disease and in the neuronal migration process using the APP/PS1 Alzheimer'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'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's based on senolytic compounds or pro-neurogenic factors.

Indexed as

Alzheimer DiseaseNeural Stem CellsAnimalsCell MovementLateral VentriclesMiceNeurogenesisOlfactory BulbBeta-amyloid toxicityNeurogenesisOlfactionSenescenceSubventricular zone

Identifiers

PMID34894324
PMCPMC8857127
OpenAlexW4200481299

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.