Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 채영규 | - |
dc.date.accessioned | 2019-10-08T01:03:27Z | - |
dc.date.available | 2019-10-08T01:03:27Z | - |
dc.date.issued | 2019-04 | - |
dc.identifier.citation | JOURNAL OF BIOLOGICAL CHEMISTRY, v. 294, NO 21, Page. 8424-8437 | en_US |
dc.identifier.issn | 0021-9258 | - |
dc.identifier.issn | 1083-351X | - |
dc.identifier.uri | http://www.jbc.org/content/294/21/8424 | - |
dc.identifier.uri | https://repository.hanyang.ac.kr/handle/20.500.11754/110907 | - |
dc.description.abstract | Mesenchymal stromal cells (MSCs) can potently regulate the functions of immune cells and are being investigated for the management of inflammatory diseases. Toll-like receptor 3 (TLR3)-stimulated human MSCs (hMSCs) exhibit increased migration and chemotaxis within and toward damaged tissues. However, the regulatory mechanisms underlying these migratory activities are unclear. Therefore, we analyzed the migration capability and gene expression profiles of TLR3-stimulated hMSCs using RNA-Seq, wound healing, and transwell cell migration assay. Along with increased cell migration, the TLR3 stimulation also increased the expression of cytokines, chemokines, and cell migration-related genes. The promoter regions of the latter showed an enrichment of putative motifs for binding the transcription factors forkhead box O1 (FOXO1), FOXO3, NF-kB (NF-kB1), and RELA proto-oncogene and NF-kB subunit. Of note, FOXO1 inhibition by the FOXO1-selective inhibitor AS1842856 significantly reduced both migration and the expression of migration-related genes. In summary, our results indicate that TLR3 stimulation induces hMSC migration through the expression of FOXO1-activated genes. © 2019 American Society for Biochemistry and Molecular Biology Inc. All rights reserved. | en_US |
dc.description.sponsorship | This work was supported by National Research Foundation of Korea (NRF) Grants 2017M3A9G7073033, 2017R1A2B4012905, and 2011-0030049 (to Y. G. C.) and 2016R1D1A1B04934970 (to K. H. J.) from the Korean govern-ment. The authors declare that they have no conflicts of interest with the contents of this article. | en_US |
dc.language.iso | en | en_US |
dc.publisher | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | en_US |
dc.subject | mesenchymal stem cells (MSCs) | en_US |
dc.subject | Toll-like receptor (TLR) | en_US |
dc.subject | gene expression | en_US |
dc.subject | cell migration | en_US |
dc.subject | transcriptomics | en_US |
dc.subject | forkhead box protein O | en_US |
dc.subject | polyinosinic:polycytidylic acid | en_US |
dc.subject | RNA-sequencing | en_US |
dc.title | Forkhead box O1 (FOXO1) controls the migratory response of Toll-like receptor (TLR3)-stimulated human mesenchymal stromalcells | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1074/jbc.RA119.008673 | - |
dc.relation.page | 1-15 | - |
dc.relation.journal | JOURNAL OF BIOLOGICAL CHEMISTRY | - |
dc.contributor.googleauthor | Kim, Sun Hwa | - |
dc.contributor.googleauthor | Das, Amitabh | - |
dc.contributor.googleauthor | Choi, Hae In | - |
dc.contributor.googleauthor | Kim, Ki Hoon | - |
dc.contributor.googleauthor | Chai, Jin Choul | - |
dc.contributor.googleauthor | Choi, Mi Ran | - |
dc.contributor.googleauthor | Binas, Bert | - |
dc.contributor.googleauthor | Park, Kyoung Sun | - |
dc.contributor.googleauthor | Lee, Young Seek | - |
dc.contributor.googleauthor | Chai, Young Gyu | - |
dc.relation.code | 2019002362 | - |
dc.sector.campus | S | - |
dc.sector.daehak | GRADUATE SCHOOL[S] | - |
dc.sector.department | DEPARTMENT OF BIONANOTECHNOLOGY | - |
dc.identifier.pid | ygchai | - |
dc.identifier.orcid | https://orcid.org/0000-0002-3333-4803 | - |
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