Age-dependent changes in Wnt signaling components and synapse number are differentially affected between brain regions.


Journal

Experimental gerontology
ISSN: 1873-6815
Titre abrégé: Exp Gerontol
Pays: England
ID NLM: 0047061

Informations de publication

Date de publication:
08 2022
Historique:
received: 02 03 2022
accepted: 23 05 2022
pubmed: 2 6 2022
medline: 1 7 2022
entrez: 1 6 2022
Statut: ppublish

Résumé

Wnt signaling plays an important role in adult brain function, and its dysregulation has been implicated in functional decline during aging as well as in some neurodegenerative diseases, such as Alzheimer's disease. In the adult brain, the Wnt pathway contributes to synapse formation and maintenance, axonal remodeling, and dendrite outgrowth. Recent findings indicate a downregulation of Wnt signaling in the aged brain in different models, but it has not been associated with changes in the number and structure of central synapses. The expression and distribution of Wnt components in different brain regions may vary with age, which may have important implications for brain homeostasis manifesting as different behavioral alterations. Thus, in the present work, we analyzed the expression levels and protein content of different molecules of the Wnt pathway in young and aged rats in the cerebral cortex, hippocampus and cerebellum and discussed their correlation with changes in synaptic number and morphology.

Identifiants

pubmed: 35642846
pii: S0531-5565(22)00162-0
doi: 10.1016/j.exger.2022.111854
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

111854

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Lizbeth García-Velázquez (L)

Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, AP 70-228, 04510 México DF, Mexico.

Paulina López-Carrasco (P)

Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, AP 70-228, 04510 México DF, Mexico.

Clorinda Arias (C)

Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, AP 70-228, 04510 México DF, Mexico. Electronic address: carias@unam.mx.

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Classifications MeSH