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• W2777760175 abstract "The underlying cellular mechanisms of catatonia, an executive psychomotor syndrome that is observed across neuropsychiatric diseases, have remained obscure. In humans and mice, reduced expression of the structural myelin protein CNP is associated with catatonic signs in an age-dependent manner, pointing to the involvement of myelin-producing oligodendrocytes. Here, we showed that the underlying cause of catatonic signs is the low-grade inflammation of white matter tracts, which marks a final common pathway in Cnp-deficient and other mutant mice with minor myelin abnormalities. The inhibitor of CSF1 receptor kinase signaling PLX5622 depleted microglia and alleviated the catatonic symptoms of Cnp mutants. Thus, microglia and low-grade inflammation of myelinated tracts emerged as the trigger of a previously unexplained mental condition. We observed a very high (25%) prevalence of individuals with catatonic signs in a deeply phenotyped schizophrenia sample (n = 1095). Additionally, we found the loss-of-function allele of a myelin-specific gene (CNP rs2070106-AA) associated with catatonia in 2 independent schizophrenia cohorts and also associated with white matter hyperintensities in a general population sample. Since the catatonic syndrome is likely a surrogate marker for other executive function defects, we suggest that microglia-directed therapies may be considered in psychiatric disorders associated with myelin abnormalities." @default.
• W2777760175 created "2018-01-05" @default.
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• W2777760175 date "2017-12-18" @default.
• W2777760175 modified "2023-10-13" @default.
• W2777760175 title "Microglia ablation alleviates myelin-associated catatonic signs in mice" @default.
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• W2777760175 doi "https://doi.org/10.1172/jci97032" @default.
• W2777760175 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5785265" @default.
• W2777760175 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29252214" @default.
• W2777760175 hasPublicationYear "2017" @default.
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