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Insulin and insulin-like growth factor-I receptors in astrocytes exert different effects on behavior and Alzheimer ́s-like pathology

  • ,
  • Ana M. Fernandez
    ,
  • Laura Martinez-Rachadell
    ,
  • Raquel Herrero-Labrador
    ,
  • Jansen Fernandes
    ,
  • Ignacio Torres Aleman
  • ,
  • Universidad Señor de Sipán
    ,
  • Instituto de Salud Carlos III
    ,
  • Achucarro Basque Center for Neuroscience
    ,
  • Cajal Institute (CSIC)
    ,
  • Universidade Federal de São Paulo
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Page 663 (1 page)

Journal (Volume, Issue Number)

F1000Research (Volume 11)

Publication milestones

  • Published - 2022

Publication status

Published - 2022

ISSN

2046-1402

Publication IDs

  • Scopus: 85146195280
  • PubMed: 36636477

Abstract

Background: Pleiotropic actions of insulin and insulin-like growth factor I (IGF-I) in the brain are context- and cell-dependent, but whether this holds for their receptors (insulin receptor (IR) and IGF-I receptor (IGF-IR), respectively), is less clear. Methods: We compared mice lacking IR or IGF-IR in glial fibrillary astrocytic protein (GFAP)-expressing astrocytes in a tamoxifen-regulated manner, to clarify their role in this type of glial cells, as the majority of data of their actions in brain have been obtained in neurons. Results: We observed that mice lacking IR in GFAP astrocytes (GFAP IR KO mice) develop mood disturbances and maintained intact cognition, while at the same time show greater pathology when cross-bred with APP/PS1 mice, a model of familial Alzheimer´s disease (AD). Conversely, mice lacking IGF-IR in GFAP astrocytes (GFAP-IGF-IR KO mice) show cognitive disturbances, maintained mood tone, and show control-dependent changes in AD-like pathology. Conclusions: These observations confirm that the role of IR and IGF-IR in the brain is cell-specific and context-dependent.

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