Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/65772
DC Field | Value | Language |
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dc.contributor | Department of Health Technology and Informatics | - |
dc.creator | Chen, YB | - |
dc.creator | Zhou, Y | - |
dc.creator | Wang, J | - |
dc.creator | Wang, LH | - |
dc.creator | Zou, X | - |
dc.creator | Li, DM | - |
dc.creator | Han, X | - |
dc.date.accessioned | 2017-05-22T02:09:13Z | - |
dc.date.available | 2017-05-22T02:09:13Z | - |
dc.identifier.uri | http://hdl.handle.net/10397/65772 | - |
dc.language.iso | en | en_US |
dc.publisher | Nature Publishing Group | en_US |
dc.rights | This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license,users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ | en_US |
dc.rights | © The Author(s) 2016 | en_US |
dc.rights | The following publication Chen, Y., Zhou, Y., Wang, J., Wang, L., Xiang, Z., Li, D., & Han, X. (2016). Microcystin-Leucine Arginine causes cytotoxic effects in sertoli cells resulting in reproductive dysfunction in male mice. Scientific reports, 6, 39238 is available at http://dx.doi.org/10.1038/srep39238 | en_US |
dc.title | Microcystin-leucine arginine causes cytotoxic effects in sertoli cells resulting in reproductive dysfunction in male mice | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.spage | 1 | en_US |
dc.identifier.epage | 18 | en_US |
dc.identifier.volume | 6 | en_US |
dc.identifier.doi | 10.1038/srep39238 | en_US |
dcterms.abstract | Microcystin-leucine arginine (MC-LR) is a potent toxin for Sertoli cells. However, the specific molecular mechanisms of MC-induced cytotoxicity still remain unclear. In this study, we performed a comprehensive analyses of changes of miRNAs and mRNAs in Sertoli cells treated with MC-LR. Through computational approaches, we showed the pivotal roles of differentially expressed miRNAs that were associated with cell metabolism, cellular growth and proliferation, cell-to-cell signaling and interaction and cellular movement. Ingenuity Pathway Analyses (IPA) revealed some differentially expressed miRNAs and mRNAs that may cause reproductive system diseases. Target gene analyses suggested that destruction in tight junctions (TJ) and adherens junctions (AJ) in testes may be mediated by miRNAs. Consistent with a significant enrichment of chemokine signaling pathways, we observed numerous macrophages in the testes of mice following treatment with MC-LR, which may cause testicular inflammation. Moreover, miR-98-5p and miR-758 were predicted to bind the 3′-UTR region of the mitogen-activated protein kinase 11 (MAPK11, p38 β isoform) gene which stimulates tumor necrosis factor-α (TNF-α) expression in Sertoli cells. TNF-α could interact with the tumor necrosis factor receptor 1 (TNFR1) on germ cells leading to induction of germ cell apoptosis. Collectively, our integrated miRNA/mRNA analyses provided a molecular paradigm, which was experimentally validated, for understanding MC-LR-induced cytotoxicity. | - |
dcterms.accessRights | open access | en_US |
dcterms.bibliographicCitation | Scientific reports, 2016, v. 6, 39238, p. 1-18 | - |
dcterms.isPartOf | Scientific reports | - |
dcterms.issued | 2016 | - |
dc.identifier.isi | WOS:000390280100001 | - |
dc.identifier.scopus | 2-s2.0-85006264088 | - |
dc.identifier.ros | 2016003426 | - |
dc.identifier.eissn | 2045-2322 | en_US |
dc.identifier.artn | 39238 | en_US |
dc.identifier.rosgroupid | 2016003357 | - |
dc.description.ros | 2016-2017 > Academic research: refereed > Publication in refereed journal | - |
dc.description.validate | 201804_a bcma | - |
dc.description.oa | Version of Record | en_US |
dc.identifier.FolderNumber | a0106-n03 | en_US |
dc.description.pubStatus | Published | en_US |
dc.description.oaCategory | CC | en_US |
Appears in Collections: | Journal/Magazine Article |
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File | Description | Size | Format | |
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srep39238.pdf | 3.66 MB | Adobe PDF | View/Open |
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