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.
Authors
- Maura McGrail (ORCID: https://orcid.org/0000-0001-9308-6189)
- Anumantha G. Kanthasamy (ORCID: https://orcid.org/0000-0002-6454-4264)
- Sahiba Siddiqui (ORCID: https://orcid.org/0009-0002-0340-1937)
- Fang Liu (ORCID: https://orcid.org/0000-0002-8325-1213)
Institutions
- University of Georgia (US)
- Iowa State University (US)
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
Funders
- Iowa State University
- National Institutes of Health