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Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids

Although congenital infection by human cytomegalovirus (HCMV) is well recognized as a leading cause of neurodevelopmental defects, HCMV neuropathogenesis remains poorly understood. A major challenge for investigating HCMV-induced abnormal brain development is the strict CMV species specificity, whic...

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Autores principales: Sun, Guoqiang, Chiuppesi, Flavia, Chen, Xianwei, Wang, Cheng, Tian, E, Nguyen, Jenny, Kha, Mindy, Trinh, Daniel, Zhang, Hannah, Marchetto, Maria C., Song, Hongjun, Ming, Guo-Li, Gage, Fred H., Diamond, Don J., Wussow, Felix, Shi, Yanhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659592/
https://www.ncbi.nlm.nih.gov/pubmed/33205055
http://dx.doi.org/10.1016/j.xcrm.2020.100002
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author Sun, Guoqiang
Chiuppesi, Flavia
Chen, Xianwei
Wang, Cheng
Tian, E
Nguyen, Jenny
Kha, Mindy
Trinh, Daniel
Zhang, Hannah
Marchetto, Maria C.
Song, Hongjun
Ming, Guo-Li
Gage, Fred H.
Diamond, Don J.
Wussow, Felix
Shi, Yanhong
author_facet Sun, Guoqiang
Chiuppesi, Flavia
Chen, Xianwei
Wang, Cheng
Tian, E
Nguyen, Jenny
Kha, Mindy
Trinh, Daniel
Zhang, Hannah
Marchetto, Maria C.
Song, Hongjun
Ming, Guo-Li
Gage, Fred H.
Diamond, Don J.
Wussow, Felix
Shi, Yanhong
author_sort Sun, Guoqiang
collection PubMed
description Although congenital infection by human cytomegalovirus (HCMV) is well recognized as a leading cause of neurodevelopmental defects, HCMV neuropathogenesis remains poorly understood. A major challenge for investigating HCMV-induced abnormal brain development is the strict CMV species specificity, which prevents the use of animal models to directly study brain defects caused by HCMV. We show that infection of human-induced pluripotent-stem-cell-derived brain organoids by a “clinical-like” HCMV strain results in reduced brain organoid growth, impaired formation of cortical layers, and abnormal calcium signaling and neural network activity. Moreover, we show that the impeded brain organoid development caused by HCMV can be prevented by neutralizing antibodies (NAbs) that recognize the HCMV pentamer complex. These results demonstrate in a three-dimensional cellular biosystem that HCMV can impair the development and function of the human brain and provide insights into the potential capacity of NAbs to mitigate brain defects resulted from HCMV infection.
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spelling pubmed-76595922020-11-16 Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids Sun, Guoqiang Chiuppesi, Flavia Chen, Xianwei Wang, Cheng Tian, E Nguyen, Jenny Kha, Mindy Trinh, Daniel Zhang, Hannah Marchetto, Maria C. Song, Hongjun Ming, Guo-Li Gage, Fred H. Diamond, Don J. Wussow, Felix Shi, Yanhong Cell Rep Med Article Although congenital infection by human cytomegalovirus (HCMV) is well recognized as a leading cause of neurodevelopmental defects, HCMV neuropathogenesis remains poorly understood. A major challenge for investigating HCMV-induced abnormal brain development is the strict CMV species specificity, which prevents the use of animal models to directly study brain defects caused by HCMV. We show that infection of human-induced pluripotent-stem-cell-derived brain organoids by a “clinical-like” HCMV strain results in reduced brain organoid growth, impaired formation of cortical layers, and abnormal calcium signaling and neural network activity. Moreover, we show that the impeded brain organoid development caused by HCMV can be prevented by neutralizing antibodies (NAbs) that recognize the HCMV pentamer complex. These results demonstrate in a three-dimensional cellular biosystem that HCMV can impair the development and function of the human brain and provide insights into the potential capacity of NAbs to mitigate brain defects resulted from HCMV infection. Elsevier 2020-03-25 /pmc/articles/PMC7659592/ /pubmed/33205055 http://dx.doi.org/10.1016/j.xcrm.2020.100002 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sun, Guoqiang
Chiuppesi, Flavia
Chen, Xianwei
Wang, Cheng
Tian, E
Nguyen, Jenny
Kha, Mindy
Trinh, Daniel
Zhang, Hannah
Marchetto, Maria C.
Song, Hongjun
Ming, Guo-Li
Gage, Fred H.
Diamond, Don J.
Wussow, Felix
Shi, Yanhong
Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids
title Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids
title_full Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids
title_fullStr Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids
title_full_unstemmed Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids
title_short Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids
title_sort modeling human cytomegalovirus-induced microcephaly in human ipsc-derived brain organoids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659592/
https://www.ncbi.nlm.nih.gov/pubmed/33205055
http://dx.doi.org/10.1016/j.xcrm.2020.100002
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