Cerebellar Development and Autism Spectrum Disorder in Tuberous Sclerosis Complex

被引:33
|
作者
Sundberg, Maria [1 ]
Sahin, Mustafa [1 ]
机构
[1] Harvard Univ, Childrens Hosp Boston, FM Kirby Neurobiol Ctr, Dept Neurol,Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
magnetic resonance imaging; mouse models; mechanistic target of rapamycin; Purkinje cell; cerebellum; PLURIPOTENT STEM-CELLS; TSC2 GAP ACTIVITY; PURKINJE-CELLS; CORTICAL TUBERS; STEREOLOGICAL EXPERIMENT; ISTHMIC ORGANIZER; IMAGING FINDINGS; RODENT MODELS; BRAIN; CHILDREN;
D O I
10.1177/0883073815600870
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Approximately 50% of patients with the genetic disease tuberous sclerosis complex present with autism spectrum disorder. Although a number of studies have investigated the link between autism and tuberous sclerosis complex, the etiology of autism spectrum disorder in these patients remains unclear. Abnormal cerebellar function during critical phases of development could disrupt functional processes in the brain, leading to development of autistic features. Accordingly, the authors review the potential role of cerebellar dysfunction in the pathogenesis of autism spectrum disorder in tuberous sclerosis complex. The authors also introduce conditional knockout mouse models of Tsc1 and Tsc2 that link cerebellar circuitry to the development of autistic-like features. Taken together, these preclinical and clinical investigations indicate the cerebellum has a profound regulatory role during development of social communication and repetitive behaviors.
引用
收藏
页码:1954 / 1962
页数:9
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