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- Publisher Website: 10.1016/j.celrep.2017.09.047
- Scopus: eid_2-s2.0-85030862076
- PMID: 29020636
- WOS: WOS:000412686100020
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Article: Self-Organized Cerebral Organoids with Human-Specific Features Predict Effective Drugs to Combat Zika Virus Infection
Title | Self-Organized Cerebral Organoids with Human-Specific Features Predict Effective Drugs to Combat Zika Virus Infection |
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Authors | Watanabe, MomokoButh, Jessie E.Vishlaghi, Nedade la Torre-Ubieta, LuisTaxidis, JiannisKhakh, Baljit S.Coppola, GiovanniPearson, Caroline A.Yamauchi, KenGong, DanyangDai, XinghongDamoiseaux, RobertAliyari, RoghiyhLiebscher, SimoneSchenke-Layland, KatjaCaneda, ChristineHuang, Eric J.Zhang, YeCheng, GenhongGeschwind, Daniel H.Golshani, PeymanSun, RenNovitch, Bennett G. |
Keywords | neural development cerebral cortex differentiation embryonic stem cell human brain neural stem cell neurogenesis organoid Zika virus |
Issue Date | 2017 |
Citation | Cell Reports, 2017, v. 21, n. 2, p. 517-532 How to Cite? |
Abstract | © 2017 The Author(s) The human cerebral cortex possesses distinct structural and functional features that are not found in the lower species traditionally used to model brain development and disease. Accordingly, considerable attention has been placed on the development of methods to direct pluripotent stem cells to form human brain-like structures termed organoids. However, many organoid differentiation protocols are inefficient and display marked variability in their ability to recapitulate the three-dimensional architecture and course of neurogenesis in the developing human brain. Here, we describe optimized organoid culture methods that efficiently and reliably produce cortical and basal ganglia structures similar to those in the human fetal brain in vivo. Neurons within the organoids are functional and exhibit network-like activities. We further demonstrate the utility of this organoid system for modeling the teratogenic effects of Zika virus on the developing brain and identifying more susceptibility receptors and therapeutic compounds that can mitigate its destructive actions. Cerebral organoids recapitulate many aspects of human corticogenesis and are a useful platform for modeling neurodevelopmental mechanisms and diseases. Watanabe et al. describe enhanced organoid methods and model ZIKV pathology. More susceptibility receptors for ZIKV are identified, and differential effects of various compounds to mitigate ZIKV-induced cytopathy are demonstrated. |
Persistent Identifier | http://hdl.handle.net/10722/285959 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Watanabe, Momoko | - |
dc.contributor.author | Buth, Jessie E. | - |
dc.contributor.author | Vishlaghi, Neda | - |
dc.contributor.author | de la Torre-Ubieta, Luis | - |
dc.contributor.author | Taxidis, Jiannis | - |
dc.contributor.author | Khakh, Baljit S. | - |
dc.contributor.author | Coppola, Giovanni | - |
dc.contributor.author | Pearson, Caroline A. | - |
dc.contributor.author | Yamauchi, Ken | - |
dc.contributor.author | Gong, Danyang | - |
dc.contributor.author | Dai, Xinghong | - |
dc.contributor.author | Damoiseaux, Robert | - |
dc.contributor.author | Aliyari, Roghiyh | - |
dc.contributor.author | Liebscher, Simone | - |
dc.contributor.author | Schenke-Layland, Katja | - |
dc.contributor.author | Caneda, Christine | - |
dc.contributor.author | Huang, Eric J. | - |
dc.contributor.author | Zhang, Ye | - |
dc.contributor.author | Cheng, Genhong | - |
dc.contributor.author | Geschwind, Daniel H. | - |
dc.contributor.author | Golshani, Peyman | - |
dc.contributor.author | Sun, Ren | - |
dc.contributor.author | Novitch, Bennett G. | - |
dc.date.accessioned | 2020-08-18T04:57:05Z | - |
dc.date.available | 2020-08-18T04:57:05Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Cell Reports, 2017, v. 21, n. 2, p. 517-532 | - |
dc.identifier.uri | http://hdl.handle.net/10722/285959 | - |
dc.description.abstract | © 2017 The Author(s) The human cerebral cortex possesses distinct structural and functional features that are not found in the lower species traditionally used to model brain development and disease. Accordingly, considerable attention has been placed on the development of methods to direct pluripotent stem cells to form human brain-like structures termed organoids. However, many organoid differentiation protocols are inefficient and display marked variability in their ability to recapitulate the three-dimensional architecture and course of neurogenesis in the developing human brain. Here, we describe optimized organoid culture methods that efficiently and reliably produce cortical and basal ganglia structures similar to those in the human fetal brain in vivo. Neurons within the organoids are functional and exhibit network-like activities. We further demonstrate the utility of this organoid system for modeling the teratogenic effects of Zika virus on the developing brain and identifying more susceptibility receptors and therapeutic compounds that can mitigate its destructive actions. Cerebral organoids recapitulate many aspects of human corticogenesis and are a useful platform for modeling neurodevelopmental mechanisms and diseases. Watanabe et al. describe enhanced organoid methods and model ZIKV pathology. More susceptibility receptors for ZIKV are identified, and differential effects of various compounds to mitigate ZIKV-induced cytopathy are demonstrated. | - |
dc.language | eng | - |
dc.relation.ispartof | Cell Reports | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | neural development | - |
dc.subject | cerebral cortex | - |
dc.subject | differentiation | - |
dc.subject | embryonic stem cell | - |
dc.subject | human brain | - |
dc.subject | neural stem cell | - |
dc.subject | neurogenesis | - |
dc.subject | organoid | - |
dc.subject | Zika virus | - |
dc.title | Self-Organized Cerebral Organoids with Human-Specific Features Predict Effective Drugs to Combat Zika Virus Infection | - |
dc.type | Article | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1016/j.celrep.2017.09.047 | - |
dc.identifier.pmid | 29020636 | - |
dc.identifier.pmcid | PMC5637483 | - |
dc.identifier.scopus | eid_2-s2.0-85030862076 | - |
dc.identifier.volume | 21 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 517 | - |
dc.identifier.epage | 532 | - |
dc.identifier.eissn | 2211-1247 | - |
dc.identifier.isi | WOS:000412686100020 | - |
dc.identifier.issnl | 2211-1247 | - |