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 5â 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.
Stat3 mediates Fyn kinase-driven dopaminergic neurodegeneration and microglia activation.
Stat3介导Fyn激酶驱动的多巴胺能神经退行性变和小胶质细胞活化
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作者:Siddiqui Sahiba, Liu Fang, Kanthasamy Anumantha G, McGrail Maura
| 期刊: | Disease Models & Mechanisms | 影响因子: | 3.300 |
| 时间: | 2024 | 起止号: | 2024 Dec 1; 17(12):dmm052011 |
| doi: | 10.1242/dmm.052011 | 研究方向: | 神经科学、细胞生物学 |
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