Postnatal downregulation of Fmr1 in microglia promotes microglial reactivity and causes behavioural alterations in female mice.

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Tác giả: Nicole Brown, Weihua Cai, Jonathan Fan, Christos G Gkogkas, Mehdi Hooshmandi, David Ho-Tieng, Volodya Hovhannisyan, Arkady Khoutorsky, Kevin C Lister, Masha Prager-Khoutorsky, Nahum Sonenberg, Sonali Uttam, Calvin Wong

Ngôn ngữ: eng

Ký hiệu phân loại: 597.959 *Anguinomorphoidea

Thông tin xuất bản: England : Molecular autism , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 693438

BACKGROUND: Fragile X syndrome is caused by the loss of the Fmr1 gene expression. Deletion of Fmr1 in various neuronal and non-neuronal subpopulations in the brain of mice leads to cell-type-specific effects. Microglia, immune cells critical for the refinement of neuronal circuits during brain development, have been implicated in various neurodevelopmental disorders, including fragile X syndrome. However, it is unknown whether reduced Fmr1 expression in microglia leads to molecular and behavioral phenotypes. METHODS: We downregulated Fmr1 in microglia during early and late postnatal development and studied the effect on microglial morphology and distinct behaviours. RESULTS: Female, but not male, adult mice with downregulation of Fmr1 in microglia during early development exhibited reactive microglia and behavioral phenotypes, including enhanced self-grooming and alterations in social interaction. Downregulation of Fmr1 in microglia during late development induced a milder phenotype, characterized by impaired preference for social novelty without affecting microglia morphology. CONCLUSIONS: The downregulation of Fmr1 and its encoded protein FMRP in microglia contributes to behavioural phenotypes in a sex-specific manner.
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