PTEN in Autism and Neurodevelopmental Disorders

被引:75
|
作者
Rademacher, Sebastian [1 ]
Eickholt, Britta J. [1 ]
机构
[1] Charite Univ Med Berlin, Inst Biochem, D-10117 Berlin, Germany
来源
关键词
CELL-CYCLE EXIT; E3 LIGASE NEDD4; TENSIN HOMOLOG; BETA-CATENIN; NEURONAL DIFFERENTIATION; DOWNSTREAM TARGET; MAMMALIAN TARGET; COWDEN-SYNDROME; SELF-RENEWAL; MOUSE MODEL;
D O I
10.1101/cshperspect.a036780
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Phosphatase and tensin homolog (PTEN) is a classical tumor suppressor that antagonizes phosphatidylinositol 3-phosphate kinase (P13K)/AKT signaling. Although there is a strong association of PTEN germline mutations with cancer syndromes, they have also been described in a subset of patients with autism spectrum disorders with macrocephaly characterized by impairments in social interactions and communication, repetitive behavior and, occasionally, epilepsy. To investigate PTEN's role during neurodevelopment and its implication for autism, several conditional Pten knockout mouse models have been generated. These models are valuable tools to understand PTEN's spatiotemporal roles during neurodevelopment. In this review, we will highlight the anatomical and phenotypic results from animal studies and link them to cellular and molecular findings.
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页数:17
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