Enriched environment promotes remyelination and motor function recovery through modulation of HDAC1/2 in mice. (10th August 2017)

• Record Type: Journal Article
• Authors: Zheng, Jian; Ding, Weijun; Li, Baoming; Yang, Youjun
• Is Part Of: Neuroscience letters. Volume 655(2017)
• Page Start: 121
• Page End: 130
• Publication Date: 2017-08-10
• Subjects: Enriched environment -- Oligodendrocyte -- Remyelination -- Motor functions -- HDAC1/2; Neurology -- Periodicals; Neurology -- Periodicals; Research -- Periodicals; Neurologie -- Périodiques; Neuroanatomie -- Périodiques; Neuropharmacologie -- Périodiques; Neurophysiologie -- Périodiques; Neurology; Periodicals; Electronic journals; 617.48
• DOI: 10.1016/j.neulet.2017.06.039
• Languages: English
• ISSNs: 0304-3940

Abstract

Highlights: EE is sufficient to accelerate remyelination. EE restores motor performance and promotes learning and memory. HDAC1/2 are required for EE induced remyelination. EE Inhibits Wnt signaling pathway. Abstract: Brain structure and functions are significantly affected by enriched environment (EE). Rodent and rhesus monkeys raised in EE will increase myelination in development, and these increase correlate with improved cognitive functions on learning and memory. However, whether and how EE influences remyelination in the adult remained undefined. Here, we used a cuprizone-induced demyelination mouse model demonstrate that EE significantly enhances remyelination. This EE-regulated remyelination is associated with improved motor skills. We found that histone deacetylases 1/2 (HDAC1/2) were drastically increased in EE. EE act mechanistically by inhibition of Wnt signaling pathway during remyelination through promotion of HDAC1/2. Moreover, pharmacological inhibition of HDACs promoted Wnt signaling activation and impaired remyelination in EE. These results suggested that the effect of EE is likely to be mediated, at least in part, by elevating HDAC1/2 expression and inhibiting Wnt signal pathway, which initiates 'rewiring' of the neural network and accelerates remyelination. These findings highlighted the potential of EE as a promising noninvasive strategy to accelerate remyelination and to restore motor functions for demyelination related disease.