Document Type

Article

Publication Date

8-19-2025

Comments

This article is the author's final published version in Frontiers in Immunology, Volume 16, August 2025, Article Number 1617074.

The published version is available at https://doi.org/10.3389/fimmu.2025.1617074. Copyright © Azizi, Rasouli, Naziri, Gonzalez, Garifallou, Zhang, Ciric and Rostami. First published in Frontiers In Immunology.

Abstract

INTRODUCTION: GM-CSF is a pro-inflammatory cytokine that promotes an inflammatory phenotype in myeloid cells. The extent and pattern of GM-CSF expression in immune cells have not been fully elucidated. Our goal was to advance this topic using novel GM-CSF reporter/fate reporter transgenic mice.

METHODS: We tracked ongoing and past GM-CSF expression in various immune cells from multiple organs, in steady-state and autoimmune inflammation of the central nervous system (CNS).

RESULTS: The GM-CSF expression patterns varied by cell type and organ, with CD4

DISCUSSION: These findings identified distinct GM-CSF cellular sources across organs, highlighting the transient nature of GM-CSF expression and the correlation between its expression and the overall phenotype of effector memory CD4

Creative Commons License

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.

PubMed ID

40904462

Language

English

Included in

Neurology Commons

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