Copine1 regulates neural stem cell functions during brain development

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dc.contributor.authorTae Hwan Kim-
dc.contributor.authorSoo Eun Sung-
dc.contributor.authorJ C Yoo-
dc.contributor.authorJ Y Park-
dc.contributor.authorG S Yi-
dc.contributor.authorJ Y Heo-
dc.contributor.authorJae-Ran Lee-
dc.contributor.authorNam-Soon Kim-
dc.contributor.authorDa Yong Lee-
dc.date.accessioned2020-09-24T02:13:24Z-
dc.date.available2020-09-24T02:13:24Z-
dc.date.issued2018-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/22600-
dc.description.abstractCopine 1 (CPNE1) is a well-known phospholipid binding protein in plasma membrane of various cell types. In brain cells, CPNE1 is closely associated with AKT signaling pathway, which is important for neural stem cell (NSC) functions during brain development. Here, we investigated the role of CPNE1 in the regulation of brain NSC functions during brain development and determined its underlying mechanism. In this study, abundant expression of CPNE1 was observed in neural lineage cells including NSCs and immature neurons in human. With mouse brain tissues in various developmental stages, we found that CPNE1 expression was higher at early embryonic stages compared to postnatal and adult stages. To model developing brain in vitro, we used primary NSCs derived from mouse embryonic hippocampus. Our in vitro study shows decreased proliferation and multi-lineage differentiation potential in CPNE1 deficient NSCs. Finally, we found that the deficiency of CPNE1 downregulated mTOR signaling in embryonic NSCs. These data demonstrate that CPNE1 plays a key role in the regulation of NSC functions through the activation of AKT-mTOR signaling pathway during brain development.-
dc.publisherElsevier-
dc.titleCopine1 regulates neural stem cell functions during brain development-
dc.title.alternativeCopine1 regulates neural stem cell functions during brain development-
dc.typeArticle-
dc.citation.titleBiochemical and Biophysical Research Communications-
dc.citation.number1-
dc.citation.endPage173-
dc.citation.startPage168-
dc.citation.volume495-
dc.contributor.affiliatedAuthorTae Hwan Kim-
dc.contributor.affiliatedAuthorSoo Eun Sung-
dc.contributor.affiliatedAuthorJae-Ran Lee-
dc.contributor.affiliatedAuthorNam-Soon Kim-
dc.contributor.affiliatedAuthorDa Yong Lee-
dc.contributor.alternativeName김태환-
dc.contributor.alternativeName성수은-
dc.contributor.alternativeName유재철-
dc.contributor.alternativeName박재용-
dc.contributor.alternativeName이관수-
dc.contributor.alternativeName허준영-
dc.contributor.alternativeName이재란-
dc.contributor.alternativeName김남순-
dc.contributor.alternativeName이다용-
dc.identifier.bibliographicCitationBiochemical and Biophysical Research Communications, vol. 495, no. 1, pp. 168-173-
dc.identifier.doi10.1016/j.bbrc.2017.10.167-
dc.subject.keywordCopine1-
dc.subject.keywordGliogenesis-
dc.subject.keywordmTOR-
dc.subject.keywordNeural stem cell-
dc.subject.keywordNeurogenesis-
dc.subject.localCopine1-
dc.subject.localgliogenesis-
dc.subject.localGliogenesis-
dc.subject.localmTOR-
dc.subject.localneural stem cell-
dc.subject.localNeural stem cell-
dc.subject.localNeural stem cells-
dc.subject.localNeural stem cells (NSCs)-
dc.subject.localneurogenesis-
dc.subject.localNeurogenesis-
dc.description.journalClassY-
Appears in Collections:
Synthetic Biology and Bioengineering Research Institute > Genome Editing Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Genomic Medicine Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Biotherapeutics Translational Research Center > 1. Journal Articles
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