JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder

被引:13
作者
Li, Heli [1 ]
Wang, Xinyuan [1 ]
Hu, Cong [1 ]
Li, Hao [2 ]
Xu, Zhuoshuo [3 ]
Lei, Ping [3 ]
Luo, Xiaoping [4 ]
Hao, Yan [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Pediat,Div Child Healthcare, Wuhan, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Wuhan, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Basic Med, Dept Immunol, Wuhan, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Pediat, Wuhan, Peoples R China
关键词
autism; JUN; PDGFRA; cerebellum; DEGs; MATERNAL IMMUNE ACTIVATION; NETWORK-BASED METAANALYSIS; EXPRESSION; SYMPTOMS; STRESS; MODELS; CELLS; JNK1; TH17;
D O I
10.3389/fninf.2022.800079
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder, characterized by marked genetic heterogeneity. In this study, two independent microarray datasets of cerebellum of ASD were integrative analyzed by NetworkAnalyst to screen candidate crucial genes. NetworkAnalyst identified two up-regulated genes, Jun proto-oncogene (JUN) and platelet derived growth factor receptor alpha (PDGFRA), as the most crucial genes in cerebellum of ASD patients. Based on KEGG pathway database, genes associated with JUN in the cerebellum highlight the pathways of Th17 cell differentiation and Th1 and Th2 cell differentiation. Genes associated with PDGFRA in the cerebellum were found enriched in pathways in EGFR tyrosine kinase inhibitor resistance and Rap1 signaling pathway. Analyzing all differentially expressed genes (DEGs) from the two datasets, Gene Set Enrichment Analysis (GSEA) brought out IL17 signaling pathway, which is related to the expression of JUN and PDGFRA. The ImmuCellAI found the elevated expression of JUN and PDGFRA correlating with increased Th17 and monocytes suggests JUN and PDGFRA may regulate Th17 cell activation and monocytes infiltrating. Mice model of maternal immune activation demonstrated that JUN and PDGFRA are up-regulated and related to the ASD-like behaviors that provide insights into the molecular mechanisms underlying the altered IL17 signaling pathway in ASD and may enable novel therapeutic strategies.
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页数:14
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共 76 条
[1]   Dysregulation of Th1, Th2, Th17, and T regulatory cell-related transcription factor signaling in children with autism [J].
Ahmad, Sheikh Fayaz ;
Zoheir, Khairy M. A. ;
Ansari, Mushtaq Ahmad ;
Nadeem, Ahmed ;
Bakheet, Saleh A. ;
AL-Ayadhi, Laila Yousef ;
Alzahrani, Mohammad Zeed ;
Al-Shabanah, Othman A. ;
Al-Harbi, Mohammed M. ;
Attia, Sabry M. .
MOLECULAR NEUROBIOLOGY, 2017, 54 (06) :4390-4400
[2]   Does the epithelial barrier hypothesis explain the increase in allergy, autoimmunity and other chronic conditions? [J].
Akdis, Cezmi A. .
NATURE REVIEWS IMMUNOLOGY, 2021, 21 (11) :739-751
[3]   Role of platelet-derived growth factors in physiology and medicine [J].
Andrae, Johanna ;
Gallini, Radiosa ;
Betsholtz, Christer .
GENES & DEVELOPMENT, 2008, 22 (10) :1276-1312
[4]   Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia [J].
Anney, Richard J. L. ;
Ripke, Stephan ;
Anttila, Verneri ;
Grove, Jakob ;
Holmans, Peter ;
Huang, Hailiang ;
Klei, Lambertus ;
Lee, Phil H. ;
Medland, Sarah E. ;
Neale, Benjamin ;
Robinson, Elise ;
Weiss, Lauren A. ;
Zwaigenbaum, Lonnie ;
Yu, Timothy W. ;
Wittemeyer, Kerstin ;
Willsey, A. Jeremy ;
Wijsman, Ellen M. ;
Werge, Thomas ;
Wassink, Thomas H. ;
Waltes, Regina ;
Walsh, Christopher A. ;
Wallace, Simon ;
Vorstman, Jacob A. S. ;
Vieland, Veronica J. ;
Vicente, Astrid M. ;
vanEngeland, Herman ;
Tsang, Kathryn ;
Thompson, Ann P. ;
Szatmari, Peter ;
Svantesson, Oscar ;
Steinberg, Stacy ;
Stefansson, Kari ;
Stefansson, Hreinn ;
State, Matthew W. ;
Soorya, Latha ;
Silagadze, Teimuraz ;
Scherer, Stephen W. ;
Schellenberg, Gerard D. ;
Sandin, Sven ;
Sanders, Stephan J. ;
Saemundsen, Evald ;
Rouleau, Guy A. ;
Roge, Bernadette ;
Roeder, Kathryn ;
Roberts, Wendy ;
Reichert, Jennifer ;
Reichenberg, Abraham ;
Rehnstrom, Karola ;
Regan, Regina ;
Poustka, Fritz .
MOLECULAR AUTISM, 2017, 8
[5]   JNK3 as a Therapeutic Target for Neurodegenerative Diseases [J].
Antoniou, Xanthi ;
Falconi, Mattia ;
Di Marino, Daniele ;
Borsello, Tiziana .
JOURNAL OF ALZHEIMERS DISEASE, 2011, 24 (04) :633-642
[6]   Resveratrol Ameliorates Dysregulation of Th1, Th2, Th17, and T Regulatory Cell-Related Transcription Factor Signaling in a BTBR T plus tf/J Mouse Model of Autism [J].
Bakheet, Saleh A. ;
Alzahrani, Mohammad Zeed ;
Ansari, Mushtaq Ahmad ;
Nadeem, Ahmed ;
Zoheir, Khairy M. A. ;
Attia, Sabry M. ;
AL-Ayadhi, Laila Yousef ;
Ahmad, Sheikh Fayaz .
MOLECULAR NEUROBIOLOGY, 2017, 54 (07) :5201-5212
[7]   SFARI Gene: an evolving database for the autism research community [J].
Banerjee-Basu, Sharmila ;
Packer, Alan .
DISEASE MODELS & MECHANISMS, 2010, 3 (3-4) :133-135
[8]   The role of glutathione redox imbalance in autism spectrum disorder: A review [J].
Bjorklund, Geir ;
Tinkov, Alexey A. ;
Hosnedlova, Bozena ;
Kizek, Rene ;
Ajsuvakova, Olga P. ;
Chirumbolo, Salvatore ;
Skalnaya, Margarita G. ;
Peana, Massimiliano ;
Dadar, Maryam ;
El-Ansary, Afaf ;
Qasem, Hanan ;
Adams, James B. ;
Aaseth, Jan ;
Skalny, Anatoly V. .
FREE RADICAL BIOLOGY AND MEDICINE, 2020, 160 :149-162
[9]   Association of Maternal Report of Infant and Toddler Gastrointestinal Symptoms With Autism Evidence From a Prospective Birth Cohort [J].
Bresnahan, Michaeline ;
Hornig, Mady ;
Schultz, Andrew F. ;
Gunnes, Nina ;
Hirtz, Deborah ;
Lie, Kari Kveim ;
Magnus, Per ;
Reichborn-Kjennerud, Ted ;
Roth, Christine ;
Schjolberg, Synnve ;
Stoltenberg, Camilla ;
Suren, Pal ;
Susser, Ezra ;
Lipkin, W. Ian .
JAMA PSYCHIATRY, 2015, 72 (05) :466-474
[10]   Cerebellar modulation of the reward circuitry and social behavior [J].
Carta, Flaria ;
Chen, Christopher H. ;
Schott, Amanda L. ;
Dorizan, Schnaude ;
Khodakhah, Kamran .
SCIENCE, 2019, 363 (6424) :248-+