Criss‐crossing autism spectrum disorder and adult neurogenesis
Autism spectrum disorder (ASD) comprises a group of multifactorial neurodevelopmental disorders primarily characterized by deficits in social interaction and repetitive behavior. Although the onset is typically in early childhood, ASD poses a lifelong challenge for both patients and caretakers. Adul...
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Veröffentlicht in: | Journal of neurochemistry 2021-11, Vol.159 (3), p.452-478 |
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description | Autism spectrum disorder (ASD) comprises a group of multifactorial neurodevelopmental disorders primarily characterized by deficits in social interaction and repetitive behavior. Although the onset is typically in early childhood, ASD poses a lifelong challenge for both patients and caretakers. Adult neurogenesis (AN) is the process by which new functional neurons are created from neural stem cells existing in the post‐natal brain. The entire event is based on a sequence of cellular processes, such as proliferation, specification of cell fate, maturation, and ultimately, synaptic integration into the existing neural circuits. Hence, AN is implicated in structural and functional brain plasticity throughout life. Accumulating evidence shows that impaired AN may underlie some of the abnormal behavioral phenotypes seen in ASD. In this review, we approach the interconnections between the molecular pathways related to AN and ASD. We also discuss existing therapeutic approaches targeting such pathways both in preclinical and clinical studies. A deeper understanding of how ASD and AN reciprocally affect one another could reveal important converging pathways leading to the emergence of psychiatric disorders.
Autism spectrum disorder (ASD) comprises a group of neurodevelopmental disorders posing, in varying degree, a life‐long challenge for both patients and caretakers. The impact of adult neurogenesis (AN) on the pathogenesis and development of ASD has not yet been fully cleared. We review the existing evidence of the molecular interplay between factors involved in the regulation of AN and the onset of ASD. The modulation of AN in ASD might lead to a better understanding and handling of ASD. Abbreviations: AN, adult neurogenesis; ASD, autism spectrum disorder; BDNF, brain‐derived neurotrophic factor; IGF, insulin‐like growth factor; NPC, neural progenitor cells; NSC, neural stem cells; SHH, sonic hedgehog; WNT, wingless‐related integration site. |
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Autism spectrum disorder (ASD) comprises a group of neurodevelopmental disorders posing, in varying degree, a life‐long challenge for both patients and caretakers. The impact of adult neurogenesis (AN) on the pathogenesis and development of ASD has not yet been fully cleared. We review the existing evidence of the molecular interplay between factors involved in the regulation of AN and the onset of ASD. The modulation of AN in ASD might lead to a better understanding and handling of ASD. Abbreviations: AN, adult neurogenesis; ASD, autism spectrum disorder; BDNF, brain‐derived neurotrophic factor; IGF, insulin‐like growth factor; NPC, neural progenitor cells; NSC, neural stem cells; SHH, sonic hedgehog; WNT, wingless‐related integration site.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/jnc.15501</identifier><language>eng</language><publisher>New York: Blackwell Publishing Ltd</publisher><subject>adult neurogenesis ; Autism ; autism spectrum disorder ; Brain ; Cell fate ; Children ; Disorders ; Fmr1 ; Functional plasticity ; Mental disorders ; Neural networks ; Neural stem cells ; Neurodevelopmental disorders ; Neurogenesis ; Neuroplasticity ; Phenotypes ; Shank3 ; Social behavior ; Social factors ; Stem cells ; Structure-function relationships</subject><ispartof>Journal of neurochemistry, 2021-11, Vol.159 (3), p.452-478</ispartof><rights>2021 The Authors. published by John Wiley & Sons Ltd on behalf of International Society for Neurochemistry</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3301-5e6c6563cca492ac84c94f9670d5c30f330761b09741f1ed3b10ac4e50246543</citedby><cites>FETCH-LOGICAL-c3301-5e6c6563cca492ac84c94f9670d5c30f330761b09741f1ed3b10ac4e50246543</cites><orcidid>0000-0001-8802-1065 ; 0000-0002-5514-1922</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjnc.15501$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjnc.15501$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids></links><search><creatorcontrib>Bicker, Frank</creatorcontrib><creatorcontrib>Nardi, Leonardo</creatorcontrib><creatorcontrib>Maier, Jannik</creatorcontrib><creatorcontrib>Vasic, Verica</creatorcontrib><creatorcontrib>Schmeisser, Michael J.</creatorcontrib><title>Criss‐crossing autism spectrum disorder and adult neurogenesis</title><title>Journal of neurochemistry</title><description>Autism spectrum disorder (ASD) comprises a group of multifactorial neurodevelopmental disorders primarily characterized by deficits in social interaction and repetitive behavior. Although the onset is typically in early childhood, ASD poses a lifelong challenge for both patients and caretakers. Adult neurogenesis (AN) is the process by which new functional neurons are created from neural stem cells existing in the post‐natal brain. The entire event is based on a sequence of cellular processes, such as proliferation, specification of cell fate, maturation, and ultimately, synaptic integration into the existing neural circuits. Hence, AN is implicated in structural and functional brain plasticity throughout life. Accumulating evidence shows that impaired AN may underlie some of the abnormal behavioral phenotypes seen in ASD. In this review, we approach the interconnections between the molecular pathways related to AN and ASD. We also discuss existing therapeutic approaches targeting such pathways both in preclinical and clinical studies. A deeper understanding of how ASD and AN reciprocally affect one another could reveal important converging pathways leading to the emergence of psychiatric disorders.
Autism spectrum disorder (ASD) comprises a group of neurodevelopmental disorders posing, in varying degree, a life‐long challenge for both patients and caretakers. The impact of adult neurogenesis (AN) on the pathogenesis and development of ASD has not yet been fully cleared. We review the existing evidence of the molecular interplay between factors involved in the regulation of AN and the onset of ASD. The modulation of AN in ASD might lead to a better understanding and handling of ASD. Abbreviations: AN, adult neurogenesis; ASD, autism spectrum disorder; BDNF, brain‐derived neurotrophic factor; IGF, insulin‐like growth factor; NPC, neural progenitor cells; NSC, neural stem cells; SHH, sonic hedgehog; WNT, wingless‐related integration site.</description><subject>adult neurogenesis</subject><subject>Autism</subject><subject>autism spectrum disorder</subject><subject>Brain</subject><subject>Cell fate</subject><subject>Children</subject><subject>Disorders</subject><subject>Fmr1</subject><subject>Functional plasticity</subject><subject>Mental disorders</subject><subject>Neural networks</subject><subject>Neural stem cells</subject><subject>Neurodevelopmental disorders</subject><subject>Neurogenesis</subject><subject>Neuroplasticity</subject><subject>Phenotypes</subject><subject>Shank3</subject><subject>Social behavior</subject><subject>Social factors</subject><subject>Stem cells</subject><subject>Structure-function relationships</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNp10L1OwzAQB3ALgUQpDLxBJBYY0t7FH0k2UFS-VMHS3XIdp3KVj2InQt14BJ6RJ8E0TEjccsvvTnd_Qi4RZhhqvm31DDkHPCITZCnGDHl-TCYASRJTYMkpOfN-C4CCCZyQ28JZ778-PrXrvLftJlJDb30T-Z3RvRuaqLS-c6VxkWrLSJVD3UetGVy3Ma3x1p-Tk0rV3lz89ilZ3S9WxWO8fH14Ku6WsaYUMOZGaMEF1VqxPFE6YzpnVS5SKLmmUAWUClxDnjKs0JR0jaA0MxwSJjijU3I9rt257m0wvpeN9drUtWpNN3iZcJHTDJIMA736Q7fd4NpwXFAZFyxLkQd1M6rD485Ucudso9xeIsifKGWIUh6iDHY-2ndbm_3_UD6_FOPENzusdKc</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Bicker, Frank</creator><creator>Nardi, Leonardo</creator><creator>Maier, Jannik</creator><creator>Vasic, Verica</creator><creator>Schmeisser, Michael J.</creator><general>Blackwell Publishing Ltd</general><scope>24P</scope><scope>WIN</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8802-1065</orcidid><orcidid>https://orcid.org/0000-0002-5514-1922</orcidid></search><sort><creationdate>202111</creationdate><title>Criss‐crossing autism spectrum disorder and adult neurogenesis</title><author>Bicker, Frank ; Nardi, Leonardo ; Maier, Jannik ; Vasic, Verica ; Schmeisser, Michael J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3301-5e6c6563cca492ac84c94f9670d5c30f330761b09741f1ed3b10ac4e50246543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>adult neurogenesis</topic><topic>Autism</topic><topic>autism spectrum disorder</topic><topic>Brain</topic><topic>Cell fate</topic><topic>Children</topic><topic>Disorders</topic><topic>Fmr1</topic><topic>Functional plasticity</topic><topic>Mental disorders</topic><topic>Neural networks</topic><topic>Neural stem cells</topic><topic>Neurodevelopmental disorders</topic><topic>Neurogenesis</topic><topic>Neuroplasticity</topic><topic>Phenotypes</topic><topic>Shank3</topic><topic>Social behavior</topic><topic>Social factors</topic><topic>Stem cells</topic><topic>Structure-function relationships</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bicker, Frank</creatorcontrib><creatorcontrib>Nardi, Leonardo</creatorcontrib><creatorcontrib>Maier, Jannik</creatorcontrib><creatorcontrib>Vasic, Verica</creatorcontrib><creatorcontrib>Schmeisser, Michael J.</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Free Archive</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bicker, Frank</au><au>Nardi, Leonardo</au><au>Maier, Jannik</au><au>Vasic, Verica</au><au>Schmeisser, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Criss‐crossing autism spectrum disorder and adult neurogenesis</atitle><jtitle>Journal of neurochemistry</jtitle><date>2021-11</date><risdate>2021</risdate><volume>159</volume><issue>3</issue><spage>452</spage><epage>478</epage><pages>452-478</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><abstract>Autism spectrum disorder (ASD) comprises a group of multifactorial neurodevelopmental disorders primarily characterized by deficits in social interaction and repetitive behavior. Although the onset is typically in early childhood, ASD poses a lifelong challenge for both patients and caretakers. Adult neurogenesis (AN) is the process by which new functional neurons are created from neural stem cells existing in the post‐natal brain. The entire event is based on a sequence of cellular processes, such as proliferation, specification of cell fate, maturation, and ultimately, synaptic integration into the existing neural circuits. Hence, AN is implicated in structural and functional brain plasticity throughout life. Accumulating evidence shows that impaired AN may underlie some of the abnormal behavioral phenotypes seen in ASD. In this review, we approach the interconnections between the molecular pathways related to AN and ASD. We also discuss existing therapeutic approaches targeting such pathways both in preclinical and clinical studies. A deeper understanding of how ASD and AN reciprocally affect one another could reveal important converging pathways leading to the emergence of psychiatric disorders.
Autism spectrum disorder (ASD) comprises a group of neurodevelopmental disorders posing, in varying degree, a life‐long challenge for both patients and caretakers. The impact of adult neurogenesis (AN) on the pathogenesis and development of ASD has not yet been fully cleared. We review the existing evidence of the molecular interplay between factors involved in the regulation of AN and the onset of ASD. The modulation of AN in ASD might lead to a better understanding and handling of ASD. Abbreviations: AN, adult neurogenesis; ASD, autism spectrum disorder; BDNF, brain‐derived neurotrophic factor; IGF, insulin‐like growth factor; NPC, neural progenitor cells; NSC, neural stem cells; SHH, sonic hedgehog; WNT, wingless‐related integration site.</abstract><cop>New York</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1111/jnc.15501</doi><tpages>27</tpages><orcidid>https://orcid.org/0000-0001-8802-1065</orcidid><orcidid>https://orcid.org/0000-0002-5514-1922</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | adult neurogenesis Autism autism spectrum disorder Brain Cell fate Children Disorders Fmr1 Functional plasticity Mental disorders Neural networks Neural stem cells Neurodevelopmental disorders Neurogenesis Neuroplasticity Phenotypes Shank3 Social behavior Social factors Stem cells Structure-function relationships |
title | Criss‐crossing autism spectrum disorder and adult neurogenesis |
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