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Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis

Neurodevelopmental disorders are often caused by chromosomal microdeletions comprising numerous contiguous genes. A subset of neurofibromatosis type 1 (NF1) patients with severe developmental delays and intellectual disability harbors such a microdeletion event on chromosome 17q11.2, involving the N...

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Autores principales: Wegscheid, Michelle L., Anastasaki, Corina, Hartigan, Kelly A., Cobb, Olivia M., Papke, Jason B., Traber, Jennifer N., Morris, Stephanie M., Gutmann, David H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278229/
https://www.ncbi.nlm.nih.gov/pubmed/34233200
http://dx.doi.org/10.1016/j.celrep.2021.109315
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author Wegscheid, Michelle L.
Anastasaki, Corina
Hartigan, Kelly A.
Cobb, Olivia M.
Papke, Jason B.
Traber, Jennifer N.
Morris, Stephanie M.
Gutmann, David H.
author_facet Wegscheid, Michelle L.
Anastasaki, Corina
Hartigan, Kelly A.
Cobb, Olivia M.
Papke, Jason B.
Traber, Jennifer N.
Morris, Stephanie M.
Gutmann, David H.
author_sort Wegscheid, Michelle L.
collection PubMed
description Neurodevelopmental disorders are often caused by chromosomal microdeletions comprising numerous contiguous genes. A subset of neurofibromatosis type 1 (NF1) patients with severe developmental delays and intellectual disability harbors such a microdeletion event on chromosome 17q11.2, involving the NF1 gene and flanking regions (NF1 total gene deletion [NF1-TGD]). Using patient-derived human induced pluripotent stem cell (hiPSC)-forebrain cerebral organoids (hCOs), we identify both neural stem cell (NSC) proliferation and neuronal maturation abnormalities in NF1-TGD hCOs. While increased NSC proliferation results from decreased NF1/RAS regulation, the neuronal differentiation, survival, and maturation defects are caused by reduced cytokine receptor-like factor 3 (CRLF3) expression and impaired RhoA signaling. Furthermore, we demonstrate a higher autistic trait burden in NF1 patients harboring a deleterious germline mutation in the CRLF3 gene (c.1166T>C, p.Leu389Pro). Collectively, these findings identify a causative gene within the NF1-TGD locus responsible for hCO neuronal abnormalities and autism in children with NF1.
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spelling pubmed-82782292021-07-14 Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis Wegscheid, Michelle L. Anastasaki, Corina Hartigan, Kelly A. Cobb, Olivia M. Papke, Jason B. Traber, Jennifer N. Morris, Stephanie M. Gutmann, David H. Cell Rep Article Neurodevelopmental disorders are often caused by chromosomal microdeletions comprising numerous contiguous genes. A subset of neurofibromatosis type 1 (NF1) patients with severe developmental delays and intellectual disability harbors such a microdeletion event on chromosome 17q11.2, involving the NF1 gene and flanking regions (NF1 total gene deletion [NF1-TGD]). Using patient-derived human induced pluripotent stem cell (hiPSC)-forebrain cerebral organoids (hCOs), we identify both neural stem cell (NSC) proliferation and neuronal maturation abnormalities in NF1-TGD hCOs. While increased NSC proliferation results from decreased NF1/RAS regulation, the neuronal differentiation, survival, and maturation defects are caused by reduced cytokine receptor-like factor 3 (CRLF3) expression and impaired RhoA signaling. Furthermore, we demonstrate a higher autistic trait burden in NF1 patients harboring a deleterious germline mutation in the CRLF3 gene (c.1166T>C, p.Leu389Pro). Collectively, these findings identify a causative gene within the NF1-TGD locus responsible for hCO neuronal abnormalities and autism in children with NF1. 2021-07-06 /pmc/articles/PMC8278229/ /pubmed/34233200 http://dx.doi.org/10.1016/j.celrep.2021.109315 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Wegscheid, Michelle L.
Anastasaki, Corina
Hartigan, Kelly A.
Cobb, Olivia M.
Papke, Jason B.
Traber, Jennifer N.
Morris, Stephanie M.
Gutmann, David H.
Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis
title Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis
title_full Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis
title_fullStr Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis
title_full_unstemmed Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis
title_short Patient-derived iPSC-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes CRLF3 as a critical regulator of neurogenesis
title_sort patient-derived ipsc-cerebral organoid modeling of the 17q11.2 microdeletion syndrome establishes crlf3 as a critical regulator of neurogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278229/
https://www.ncbi.nlm.nih.gov/pubmed/34233200
http://dx.doi.org/10.1016/j.celrep.2021.109315
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