Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/75861
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dc.contributorDepartment of Rehabilitation Sciences-
dc.creatorKang, Sen_US
dc.creatorChen, XXen_US
dc.creatorGong, SYen_US
dc.creatorYu, PPen_US
dc.creatorYau, Sen_US
dc.creatorSu, ZHen_US
dc.creatorZhou, LBen_US
dc.creatorYu, JDen_US
dc.creatorPan, GJen_US
dc.creatorShi, LLen_US
dc.date.accessioned2018-05-10T02:54:47Z-
dc.date.available2018-05-10T02:54:47Z-
dc.identifier.issn2045-2322en_US
dc.identifier.urihttp://hdl.handle.net/10397/75861-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rightsOpen Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.rights© The Author(s) 2017en_US
dc.rightsThe following publication Kang, S., Chen, X., Gong, S. et al. Characteristic analyses of a neural differentiation model from iPSC-derived neuron according to morphology, physiology, and global gene expression pattern. Sci Rep 7, 12233 (2017) is available at https://dx.doi.org/10.1038/s41598-017-12452-xen_US
dc.titleCharacteristic analyses of a neural differentiation model from iPSC-derived neuron according to morphology, physiology, and global gene expression patternen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume7en_US
dc.identifier.doi10.1038/s41598-017-12452-xen_US
dcterms.abstractInduced pluripotent stem cells (iPSCs) can differentiate into neural progenitor cells (NPC) under proper conditions. NPC can be used as a model and is a useful tool for disease mechanism exploration and drug screening. However, the characteristics of the cells in various stages from NPC to functional neurons have not been fully described. This study investigated the characteristics of iPSC-derived NPCs during differentiation. Morphological characteristics of the NPCs, including soma area, neurite length, and the number of neurite branches, were examined on selected differentiation days. Physiological functions were assessed by recordings of sodium current, spontaneous excitatory postsynaptic current (sEPSC), and spontaneous inhibitory postsynaptic current (sIPSC). Furthermore, gene expression patterns were assessed with RNA-seq. We found that NPCs derived from iPSCs can be differentiated into glutamatergic and gabaergic neurons. Cell growth peaked during differentiation day 7-12, as the soma area decreased after day 12, growth cone and the number of branches peaked at day 9 and decreased afterwards; whereas a functional synapse formed after day 23. RNA-seq analysis found that a differential expression pattern emerged by day 7. Overall, the study provides a framework for the differentiation process of hiPSC-derived NPCs.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationScientific reports, 25 Sept. 2017, v. 7, no. , 12233, p. 1-11en_US
dcterms.isPartOfScientific reportsen_US
dcterms.issued2017-09-25-
dc.identifier.isiWOS:000411648500007-
dc.identifier.scopus2-s2.0-85029899387-
dc.identifier.pmid28947763-
dc.identifier.eissn2045-2322en_US
dc.identifier.artn12233en_US
dc.identifier.rosgroupid2017001098-
dc.description.ros2017-2018 > Academic research: refereed > Publication in refereed journal-
dc.description.validate201805 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera0763-n23en_US
dc.identifier.SubFormID1517en_US
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
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