Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1783722225024630784 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8278229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wegscheidmichellel patientderivedipsccerebralorganoidmodelingofthe17q112microdeletionsyndromeestablishescrlf3asacriticalregulatorofneurogenesis AT anastasakicorina patientderivedipsccerebralorganoidmodelingofthe17q112microdeletionsyndromeestablishescrlf3asacriticalregulatorofneurogenesis AT hartigankellya patientderivedipsccerebralorganoidmodelingofthe17q112microdeletionsyndromeestablishescrlf3asacriticalregulatorofneurogenesis AT cobboliviam patientderivedipsccerebralorganoidmodelingofthe17q112microdeletionsyndromeestablishescrlf3asacriticalregulatorofneurogenesis AT papkejasonb patientderivedipsccerebralorganoidmodelingofthe17q112microdeletionsyndromeestablishescrlf3asacriticalregulatorofneurogenesis AT traberjennifern patientderivedipsccerebralorganoidmodelingofthe17q112microdeletionsyndromeestablishescrlf3asacriticalregulatorofneurogenesis AT morrisstephaniem patientderivedipsccerebralorganoidmodelingofthe17q112microdeletionsyndromeestablishescrlf3asacriticalregulatorofneurogenesis AT gutmanndavidh patientderivedipsccerebralorganoidmodelingofthe17q112microdeletionsyndromeestablishescrlf3asacriticalregulatorofneurogenesis |