Type 1 Interleukin-4 Signaling Obliterates Mouse Astroglia

Alzheimer’s disease STAT6 astroglia interleukin-4 mouse neurogenesis regeneration zebrafish

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2020
Historique:
received: 03 12 2019
accepted: 10 02 2020
entrez: 18 3 2020
pubmed: 18 3 2020
medline: 18 3 2020
Statut: epublish

Résumé

Recent findings suggest that reduced neurogenesis could be one of the underlying reasons for the exacerbated neuropathology in humans, thus restoring the neural stem cell proliferation and neurogenesis could help to circumvent some pathological aspects of Alzheimer's disease. We recently identified Interleukin-4/STAT6 signaling as a neuron-glia crosstalk mechanism that enables glial proliferation and neurogenesis in adult zebrafish brain and 3D cultures of human astroglia, which manifest neurogenic properties. In this study, by using single cell sequencing in the APP/PS1dE9 mouse model of AD, we found that IL4 receptor (

Identifiants

pubmed: 32181251
doi: 10.3389/fcell.2020.00114
pmc: PMC7057913
doi:

Types de publication

Journal Article

Langues

eng

Pagination

114

Informations de copyright

Copyright © 2020 Mashkaryan, Siddiqui, Popova, Cosacak, Bhattarai, Brandt, Govindarajan, Petzold, Reinhardt, Dahl, Lefort and Kizil.

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Auteurs

Violeta Mashkaryan (V)

German Center for Neurodegenerative Diseases Dresden, Helmholtz Association, Dresden, Germany.

Tohid Siddiqui (T)

German Center for Neurodegenerative Diseases Dresden, Helmholtz Association, Dresden, Germany.

Stanislava Popova (S)

German Center for Neurodegenerative Diseases Dresden, Helmholtz Association, Dresden, Germany.

Mehmet Ilyas Cosacak (MI)

German Center for Neurodegenerative Diseases Dresden, Helmholtz Association, Dresden, Germany.

Prabesh Bhattarai (P)

German Center for Neurodegenerative Diseases Dresden, Helmholtz Association, Dresden, Germany.

Kerstin Brandt (K)

German Center for Neurodegenerative Diseases Dresden, Helmholtz Association, Dresden, Germany.

Nambirajan Govindarajan (N)

German Center for Neurodegenerative Diseases Dresden, Helmholtz Association, Dresden, Germany.

Andreas Petzold (A)

DRESDEN-Concept Genome Center, Center for Molecular and Cellular Bioengineering, TU Dresden, Dresden, Germany.

Susanne Reinhardt (S)

DRESDEN-Concept Genome Center, Center for Molecular and Cellular Bioengineering, TU Dresden, Dresden, Germany.

Andreas Dahl (A)

DRESDEN-Concept Genome Center, Center for Molecular and Cellular Bioengineering, TU Dresden, Dresden, Germany.

Roger Lefort (R)

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, United States.

Caghan Kizil (C)

German Center for Neurodegenerative Diseases Dresden, Helmholtz Association, Dresden, Germany.
Center for Regenerative Therapies Dresden, Center for Molecular and Cellular Bioengineering, TU Dresden, Dresden, Germany.

Classifications MeSH