Cerebellar microglia-derived IL-17A mitigates autism-related behavioral and synaptic deficits
Year: 2026
Type: article
Abstract: Interleukin-17 (IL-17) is a pleiotropic cytokine produced mainly by peripheral T helper 17 cells. Yet, the brain functions of IL-17 derived from central nervous cells remain poorly understood. Here, we find an aberrant IL-17A signaling in the cerebellum of Fmr1-KO mice, a well-established genetic model for autism spectrum disorder (ASD). Cerebellar IL-17A, derived exclusively from microglia, is essential for the regulation of social behaviors by maintaining neuronal excitability and selectively suppressing inhibitory neurotransmission of Purkinje cells (PCs) in the cerebellar Crus I, a brain region critically involved in social cognition. Specific downregulation of IL-17 receptor-mediated signaling in cerebellar PCs recapitulates ASD-like social deficits and repetitive behaviors. Notably, both direct administration of IL-17A and induction of IL-17A release from cerebellar microglia by poly(I:C) effectively restore PC excitability and ameliorate ASD-like symptoms. The findings uncover an indispensable role of microglia-derived IL-17A for cerebellar social processing and suggest potential therapeutic strategies targeting IL-17A signaling for ASD.
Source: Molecular Psychiatry
Language: English
Subfield: Cognitive Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $5,490
Funders: National Natural Science Foundation of China, Ministry of Science and Technology of the People's Republic of China, Government of Jiangsu Province, Natural Science Foundation of Jiangsu Province, Natural Science Foundation of Beijing Municipality, Nanjing University, State Key Laboratory of Pharmaceutical Biotechnology, Fundamental Research Funds for the Central Universities
OpenAlex ID: W7128424128
