Persistent astrocyte activation in the fragile X mouse cerebellum

Abstract

Background: Fragile X S yndrome, the most common single gene cause of autism, results from loss of the RNA‐binding protein FMRP. Although FMRP is highly expressed in neurons, it has also recently been identified in glia. It has been postulated that in the absence of FMRP, abnormal function of non‐neuronal cells may contribute to the pathogenesis of the disorder. We previously demonstrated reduced numbers of oligodendrocyte precursor cells and delayed myelination in the cerebellum of fragile X (F mr1) knockout mice. Methods: We used quantitative western blotting and immunocytochemistry to examine the status of astrocytes and microglia in the cerebellum of F mr1 mice during development and in adulthood. Results: We report increased expression of the astrocyte marker GFAP in the cerebellum of F mr1 mice starting in the second postnatal week and persisting in to adulthood. At 2 weeks postnatal, expression of T umor N ecrosis F actor R eceptor 2 (TNFR 2) and L eukemia I nhibitory F actor (LIF) were elevated in the F mr1 KO cerebellum. In adults, expression of TNFR 2 and the glial marker S 100 β were also elevated in F mr1 knockouts, but LIF expression was not different from wild‐type mice. We found no evidence of microglial activation or neuroinflammation at any age examined. Conclusions: These findings demonstrate an atypical pattern of astrogliosis in the absence of microglial activation in F mr1 knockout mouse cerebellum. Enhanced TNFR 2 and LIF expression in young mice suggests that changes in the expression of astrocytic proteins may be an attempt to compensate for delayed myelination in the developing cerebellum of F mr1 mice.