Stat3 mediates Fyn kinase-driven dopaminergic neurodegeneration and microglia activation

The Alzheimer's disease and Parkinson's disease risk locus FYN kinase is implicated in neurodegeneration and inflammatory signaling. To investigate in vivo mechanisms of Fyn-driven neurodegeneration, we built a zebrafish neural-specific Gal4:UAS model of constitutively active FynY531F signaling. Using in vivo live imaging, we demonstrated that neural FynY531F expression leads to dopaminergic neuron loss and mitochondrial aggregation in 5 day larval brain. Dopaminergic loss coincided with microglia activation and induction of tnfa, il1b and il12a inflammatory cytokine expression. Transcriptome analysis revealed Stat3 signaling as a potential Fyn target. Chemical inhibition experiments confirmed Fyn-driven dopaminergic neuron loss, and the inflammatory response was dependent upon activation of Stat3 and NF-κB pathways. Dual chemical inhibition demonstrated that Stat3 acts synergistically with NF-κB in dopaminergic neuron degeneration. These results identify Stat3 as a novel downstream effector of Fyn signaling in neurodegeneration and inflammation.

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Publication Details

Journal
Disease Models & Mechanisms
Published
2024-12-01
DOI
https://doi.org/10.1242/dmm.052011
Citations
2
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.49

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article

Stat3 mediates Fyn kinase-driven dopaminergic neurodegeneration and microglia activation

Maura McGrail, Anumantha G. Kanthasamy, Sahiba Siddiqui, Fang Liu
2 citations
Disease Models & Mechanisms
Neuroinflammation and Neurodegeneration Mechanisms
0.49
article

Stat3 mediates Fyn kinase-driven dopaminergic neurodegeneration and microglia activation

Maura McGrail, Anumantha G. Kanthasamy, Sahiba Siddiqui, Fang Liu
article en
2 citations

Abstract

The Alzheimer's disease and Parkinson's disease risk locus FYN kinase is implicated in neurodegeneration and inflammatory signaling. To investigate in vivo mechanisms of Fyn-driven neurodegeneration, we built a zebrafish neural-specific Gal4:UAS model of constitutively active FynY531F signaling. Using in vivo live imaging, we demonstrated that neural FynY531F expression leads to dopaminergic neuron loss and mitochondrial aggregation in 5 day larval brain. Dopaminergic loss coincided with microglia activation and induction of tnfa, il1b and il12a inflammatory cytokine expression. Transcriptome analysis revealed Stat3 signaling as a potential Fyn target. Chemical inhibition experiments confirmed Fyn-driven dopaminergic neuron loss, and the inflammatory response was dependent upon activation of Stat3 and NF-κB pathways. Dual chemical inhibition demonstrated that Stat3 acts synergistically with NF-κB in dopaminergic neuron degeneration. These results identify Stat3 as a novel downstream effector of Fyn signaling in neurodegeneration and inflammation.

Disease Models & MechanismsVol. 17(12)
University of Georgia (US), Iowa State University (US)
Iowa State University, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 32%
Neuroinflammation and Neurodegeneration Mechanisms
0.49
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