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dc.contributor.authorChiola, Simone
dc.contributor.authorNapan, Kandy L.
dc.contributor.authorWang, Yueqi
dc.contributor.authorLazarenko, Roman M.
dc.contributor.authorArmstrong, Celeste J.
dc.contributor.authorCui, Jun
dc.contributor.authorShcheglovitov, Aleksandr
dc.date.accessioned2022-08-04T22:12:30Z
dc.date.available2022-08-04T22:12:30Z
dc.date.issued2021-02
dc.identifier.citationChiola, S., Napan, K. L., Wang, Y., Lazarenko, R. M., Armstrong, C. J., Cui, J., & Shcheglovitov, A. (2021). Defective AMPA-mediated synaptic transmission and morphology in human neurons with hemizygous SHANK3 deletion engrafted in mouse prefrontal cortex. Molecular psychiatry, 26(9), 4670-4686.en_US
dc.identifier.issn1359-4184
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/16997
dc.description.abstractGenetic abnormalities in synaptic proteins are common in individuals with autism; however, our understanding of the cellular and molecular mechanisms disrupted by these abnormalities is limited. SHANK3 is a postsynaptic scaffolding protein of excitatory synapses that has been found mutated or deleted in most patients with 22q13 deletion syndrome and about 2% of individuals with idiopathic autism and intellectual disability. Here, we generated CRISPR/Cas9-engineered human pluripotent stem cells (PSCs) with complete hemizygous SHANK3 deletion (SHANK3 +/–), which is the most common genetic abnormality in patients, and investigated the synaptic and morphological properties of SHANK3-deficient PSC-derived cortical neurons engrafted in the mouse prefrontal cortex. We show that human PSC-derived neurons integrate into the mouse cortex by acquiring appropriate cortical layer identities and by receiving and sending anatomical projections from/to multiple different brain regions. We also demonstrate that SHANK3-deficient human neurons have reduced AMPA-, but not NMDA- or GABA-mediated synaptic transmission and exhibit impaired dendritic arbors and spines, as compared to isogenic control neurons co-engrafted in the same brain region. Together, this study reveals specific synaptic and morphological deficits caused by SHANK3 hemizygosity in human cortical neurons at different developmental stages under physiological conditions and validates the use of co-engrafted control and mutant human neurons as a new platform for studying connectivity deficits in genetic neurodevelopmental disorders associated with autism.en_US
dc.language.isoen_USen_US
dc.publisherSpringer Science and Business Media LLCen_US
dc.titleDefective AMPA-mediated synaptic transmission and morphology in human neurons with hemizygous SHANK3 deletion engrafted in mouse prefrontal cortexen_US
dc.typeArticleen_US
mus.citation.extentfirstpage4670en_US
mus.citation.extentlastpage4686en_US
mus.citation.journaltitleMolecular Psychiatryen_US
mus.citation.volume26en_US
mus.identifier.doi10.1038/s41380-021-01023-2en_US
mus.relation.collegeCollege of Agricultureen_US
mus.relation.departmentMicrobiology & Cell Biology.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.data.thumbpage7en_US


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