Dysregulation of neuron differentiation in an autistic savant with exceptional memory

Abstract Autism spectrum disorder (ASD) is a heterogeneous group of complex neurodevelopmental disorders without a unique or definite underlying pathogenesis. Although savant syndrome is common in ASD, few models are available for studying the molecular and cellular mechanisms of this syndrome. In t...

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Main Authors: Jinjing Song, Xiujuan Yang, Ying Zhou, Lei Chen, Xu Zhang, Zhuxi Liu, Weibo Niu, Nengpeng Zhan, Xuelian Fan, Abdul Aziz Khan, Yifang Kuang, Lulu Song, Guang He, Weidong Li
Format: Article
Language:English
Published: BMC 2019-11-01
Series:Molecular Brain
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13041-019-0507-7
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language English
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author Jinjing Song
Xiujuan Yang
Ying Zhou
Lei Chen
Xu Zhang
Zhuxi Liu
Weibo Niu
Nengpeng Zhan
Xuelian Fan
Abdul Aziz Khan
Yifang Kuang
Lulu Song
Guang He
Weidong Li
spellingShingle Jinjing Song
Xiujuan Yang
Ying Zhou
Lei Chen
Xu Zhang
Zhuxi Liu
Weibo Niu
Nengpeng Zhan
Xuelian Fan
Abdul Aziz Khan
Yifang Kuang
Lulu Song
Guang He
Weidong Li
Dysregulation of neuron differentiation in an autistic savant with exceptional memory
Molecular Brain
Autistic savant
Human induced pluripotent stem cells
TBR1
PAX6
FOXP2
Neurons
author_facet Jinjing Song
Xiujuan Yang
Ying Zhou
Lei Chen
Xu Zhang
Zhuxi Liu
Weibo Niu
Nengpeng Zhan
Xuelian Fan
Abdul Aziz Khan
Yifang Kuang
Lulu Song
Guang He
Weidong Li
author_sort Jinjing Song
title Dysregulation of neuron differentiation in an autistic savant with exceptional memory
title_short Dysregulation of neuron differentiation in an autistic savant with exceptional memory
title_full Dysregulation of neuron differentiation in an autistic savant with exceptional memory
title_fullStr Dysregulation of neuron differentiation in an autistic savant with exceptional memory
title_full_unstemmed Dysregulation of neuron differentiation in an autistic savant with exceptional memory
title_sort dysregulation of neuron differentiation in an autistic savant with exceptional memory
publisher BMC
series Molecular Brain
issn 1756-6606
publishDate 2019-11-01
description Abstract Autism spectrum disorder (ASD) is a heterogeneous group of complex neurodevelopmental disorders without a unique or definite underlying pathogenesis. Although savant syndrome is common in ASD, few models are available for studying the molecular and cellular mechanisms of this syndrome. In this study, we generated urinary induced pluripotent stem cells (UiPSCs) from a 13-year-old male autistic savant with exceptional memory. The UiPSC-derived neurons of the autistic savant exhibited upregulated expression levels of ASD genes/learning difficulty-related genes, namely PAX6, TBR1 and FOXP2, accompanied by hypertrophic neural somas, enlarged spines, reduced spine density, and an increased frequency of spontaneous excitatory postsynaptic currents. Although this study involved only a single patient and a single control because of the rarity of such cases, it provides the first autistic savant UiPSC model that elucidates the potential cellular mechanisms underlying the condition.
topic Autistic savant
Human induced pluripotent stem cells
TBR1
PAX6
FOXP2
Neurons
url http://link.springer.com/article/10.1186/s13041-019-0507-7
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spelling doaj-5445dd166aaf4a45bac567f3e2bafada2020-11-25T04:11:16ZengBMCMolecular Brain1756-66062019-11-0112111210.1186/s13041-019-0507-7Dysregulation of neuron differentiation in an autistic savant with exceptional memoryJinjing Song0Xiujuan Yang1Ying Zhou2Lei Chen3Xu Zhang4Zhuxi Liu5Weibo Niu6Nengpeng Zhan7Xuelian Fan8Abdul Aziz Khan9Yifang Kuang10Lulu Song11Guang He12Weidong Li13Bio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityBio-X Institutes, Key Laboratory for the Genetics of Development and Neuropsychiatric Disorders (Ministry of Education), Shanghai Key Laboratory of Psychotic Disorders, and Brain Science and Technology Research Center, Institute of Psychology and Behavioral Sciences, Shanghai Jiao Tong UniversityAbstract Autism spectrum disorder (ASD) is a heterogeneous group of complex neurodevelopmental disorders without a unique or definite underlying pathogenesis. Although savant syndrome is common in ASD, few models are available for studying the molecular and cellular mechanisms of this syndrome. In this study, we generated urinary induced pluripotent stem cells (UiPSCs) from a 13-year-old male autistic savant with exceptional memory. The UiPSC-derived neurons of the autistic savant exhibited upregulated expression levels of ASD genes/learning difficulty-related genes, namely PAX6, TBR1 and FOXP2, accompanied by hypertrophic neural somas, enlarged spines, reduced spine density, and an increased frequency of spontaneous excitatory postsynaptic currents. Although this study involved only a single patient and a single control because of the rarity of such cases, it provides the first autistic savant UiPSC model that elucidates the potential cellular mechanisms underlying the condition.http://link.springer.com/article/10.1186/s13041-019-0507-7Autistic savantHuman induced pluripotent stem cellsTBR1PAX6FOXP2Neurons