Pten regulates neuronal arborization and social interaction in mice

被引:751
作者
Kwon, Chang-Hyuk
Luikart, Bryan W.
Powell, Craig M.
Zhou, Jing
Matheny, Sharon A.
Zhang, Wei
Li, Yanjiao
Baker, Suzanne J.
Parada, Luis F. [1 ]
机构
[1] Univ Texas, SW Med Ctr, Ctr Dev Biol, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Kent Waldrep Fdn Ctr Basic Neurosci Res Nerve Gro, Dallas, TX 75390 USA
[3] Univ Texas, SW Med Ctr, Dept Neurol, Dallas, TX 75390 USA
[4] Univ Texas, SW Med Ctr, Dept Psychiat, Dallas, TX 75390 USA
[5] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
关键词
D O I
10.1016/j.neuron.2006.03.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
CNS deletion of Pten in the mouse has revealed its roles in controlling cell size and number, thus providing compelling etiology for macrocephaly and Lhermitte-Duclos disease. PTEN mutations in individuals with autism spectrum disorders (ASD) have also been reported, although a causal link between PTEN and ASD remains unclear. In the present study, we deleted Pten in limited differentiated neuronal populations in the cerebral cortex and hippocampus of mice. Resulting mutant mice showed abnormal social interaction and exaggerated responses to sensory stimuli. We observed macrocephaly and neuronal hypertrophy, including hypertrophic and ectopic dendrites and axonal tracts with increased synapses. This abnormal morphology was associated with activation of the Akt/mTor/S6k pathway and inactivation of Gsk3 beta. Thus, our data suggest that abnormal activation of the PI3K/AKT pathway in specific neuronal populations can underlie macrocephaly and behavioral abnormalities reminiscent of certain features of human ASD.
引用
收藏
页码:377 / 388
页数:12
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