In vivo imaging reveals impaired connectivity across cortical and subcortical networks in a mouse model of DYT1 dystonia

NEUROBIOLOGY OF DISEASE

卷:95

Article

DeSimone, Jesse C.¹  Febo, Marcelo²  Shukla, Priyank¹  Ofori, Edward¹  Colon-Perez, Luis M.²  Li, Yuqing³  Vaillancourt, David E.^1,3,4 

[1] Univ Florida, Dept Appl Physiol & Kinesiol, POB 118205, Gainesville, FL 32611 USA

[2] Univ Florida, Coll Med, Dept Psychiat, Gainesville, FL USA

[3] Univ Florida, Coll Med, Dept Neurol, Gainesville, FL 32611 USA

[4] Univ Florida, Dept Biomed Engn, Gainesville, FL USA

关键词: Diffusion MRI;    DYT1 dystonia;    Free-water;    Functional connectivity;    Functional MRI;   

DOI  :  10.1016/j.nbd.2016.07.005

来源: Elsevier

【 摘 要 】

Developing in vivo functional and structural neuroimaging assays in Dyti Delta GAG heterozygous knock-in (Dyt1 KI) mice provide insight into the pathophysiology underlying DYT1 dystonia. In the current study, we examined in vivo functional connectivity of large-scale cortical and subcortical networks in Dyt1 KI mice and wild-type (WT) controls using resting-state functional magnetic resonance imaging (MRI) and an independent component analysis. In addition, using diffusion MRI we examined how structural integrity across the basal ganglia and cerebellum directly relates to impairments in functional connectivity. Compared to WT mice, Dyt1 KI mice revealed increased functional connectivity across the striatum, thalamus, and somatosensory cortex; and reduced functional connectivity in the motor and cerebellar cortices. Further, Dyt1 KI mice demonstrated elevated free water (FW) in the striatum and cerebellum compared to WT mice, and increased FW was correlated with impairments in functional connectivity across basal ganglia, cerebellum, and sensorimotor cortex. The current study provides the first in vivo MRI-based evidence in support of the hypothesis that the deletion of a 3-base pair (Delta GAG) sequence in the Dyt1 gene encoding torsinA has network level effects on in vivo functional connectivity and microstructural integrity across the sensorimotor cortex, basal ganglia, and cerebellum. (C) 2016 Elsevier Inc. All rights reserved.

【 授权许可】

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