Hsa_circ_0002468 Regulates the Neuronal Differentiation of SH-SY5Y Cells by Modulating the MiR-561/E2F8 Axis
BACKGROUND It has been shown that circular RNAs (circRNAs) play a vital role in the regulation of neuronal differentiation; however, the precise role of circRNAs in human neuronal differentiation remains largely unexplored. MATERIAL AND METHODS A dual-luciferase reporter assay was carried out to con...
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description | BACKGROUND It has been shown that circular RNAs (circRNAs) play a vital role in the regulation of neuronal differentiation; however, the precise role of circRNAs in human neuronal differentiation remains largely unexplored. MATERIAL AND METHODS A dual-luciferase reporter assay was carried out to confirm the targets of hsa_circ_0002468, miR-561, E2F8 (E2F transcription factor 8, a protein coding gene), and miR-561. We detected the expression of hsa_circ_0002468, miR-561, and E2F8 by using quantitative real-time polymerase chain reaction (qRT-PCR) analyses. In addition, we performed the functional experiments by using a BrdU (5-bromo-2'-deoxyuridine) assay and qRT-PCR analyses. RESULTS In this study, we showed that hsa_circ_0002468 can act as a sponge of miR-561 to regulate SH-SY5Y proliferation and differentiation. A bioinformatics analysis showed that hsa_circ_0002468 had a binding site that corresponded to miR-561, which was verified by dual-luciferase reporter assay. The expression of hsa_circ_0002468 was increased during SH-SY5Y differentiation and was inversely correlated with miR-561 expression. Using qRT-PCR analysis, we showed that hsa_circ_0002468 negatively regulated miR-561 in SH-SY5Y cells. Intriguingly, the overexpression of hsa_circ_0002468 increased SH-SY5Y differentiation and reduced SH-SY5Y proliferation; the suppression of hsa_circ_0002468 led to decreased SH-SY5Y differentiation levels and increased SH-SY5Y proliferation levels. Additionally, overexpression of miR-561 rescued the SH-SY5Y proliferation deficiency induced by hsa_circ_0002468 overexpression and abolished the SH-SY5Y differentiation promoted by hsa_circ_0002468. Furthermore, E2F8 was validated as a direct target of miR-561. CONCLUSIONS Our data suggested that hsa_circ_0002468 was a novel circRNA that regulated SH-SY5Y cell proliferation and differentiation via targeting the miR-561/E2F8 axis. Therefore, manipulating hsa_circ_0002468 in SH-SY5Y cells could be a novel strategy to develop novel interventions for the treatment of relevant neurological disorders. |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6462173</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2204697444</sourcerecordid><originalsourceid>FETCH-LOGICAL-c447t-d9cb7b5a7eeaa5250121449d5b650b8c62784988175dd7d980e1c619deda8e543</originalsourceid><addsrcrecordid>eNpVUc1LHDEUD9Ki1nrqveRYkNEkk8-LIKt2BbcFtx48hUzyZo3MTjSZkfrfd3RV7Ok9eL-vxw-hb5QcUiaFOVosF4eGCkH1FtqlktdVrQT59GHfQV9KuSOEaUnENtqpiRF0wu-ibl6c9TF7S6YzlxpfwWrs3AAFD7eAf8GYU-86fBrbFjL0Q3RDTD1OLV7Oq-WNuMEz6LqCmye8SOGZGvvVC3cRryoh6dEZO9f45G8sX9Hn1nUF9l_nHro-P_szm1eXv39ezE4uK8-5GqpgfKMa4RSAc4IJQhnl3ATRSEEa7SVTmhutqRIhqGA0AeolNQGC0yB4vYeON7r3Y7OG4KfU2XX2Pse1y082uWj_v_Tx1q7So5VcMqrqSeDHq0BODyOUwa5j8dObroc0FssY4dIozp-9DjZQn1MpGdp3G0rsSz926sdu-pnQ3z8me8e-FVL_A8MTiUM</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2204697444</pqid></control><display><type>article</type><title>Hsa_circ_0002468 Regulates the Neuronal Differentiation of SH-SY5Y Cells by Modulating the MiR-561/E2F8 Axis</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central Open Access</source><source>PubMed Central</source><creator>Yang, Minhui ; Xiang, Guanghong ; Yu, Dan ; Yang, Guoshuai ; He, Weifeng ; Yang, Songlin ; Zhou, Gaoya ; Liu, Aiqun</creator><creatorcontrib>Yang, Minhui ; Xiang, Guanghong ; Yu, Dan ; Yang, Guoshuai ; He, Weifeng ; Yang, Songlin ; Zhou, Gaoya ; Liu, Aiqun</creatorcontrib><description>BACKGROUND It has been shown that circular RNAs (circRNAs) play a vital role in the regulation of neuronal differentiation; however, the precise role of circRNAs in human neuronal differentiation remains largely unexplored. MATERIAL AND METHODS A dual-luciferase reporter assay was carried out to confirm the targets of hsa_circ_0002468, miR-561, E2F8 (E2F transcription factor 8, a protein coding gene), and miR-561. We detected the expression of hsa_circ_0002468, miR-561, and E2F8 by using quantitative real-time polymerase chain reaction (qRT-PCR) analyses. In addition, we performed the functional experiments by using a BrdU (5-bromo-2'-deoxyuridine) assay and qRT-PCR analyses. RESULTS In this study, we showed that hsa_circ_0002468 can act as a sponge of miR-561 to regulate SH-SY5Y proliferation and differentiation. A bioinformatics analysis showed that hsa_circ_0002468 had a binding site that corresponded to miR-561, which was verified by dual-luciferase reporter assay. The expression of hsa_circ_0002468 was increased during SH-SY5Y differentiation and was inversely correlated with miR-561 expression. Using qRT-PCR analysis, we showed that hsa_circ_0002468 negatively regulated miR-561 in SH-SY5Y cells. Intriguingly, the overexpression of hsa_circ_0002468 increased SH-SY5Y differentiation and reduced SH-SY5Y proliferation; the suppression of hsa_circ_0002468 led to decreased SH-SY5Y differentiation levels and increased SH-SY5Y proliferation levels. Additionally, overexpression of miR-561 rescued the SH-SY5Y proliferation deficiency induced by hsa_circ_0002468 overexpression and abolished the SH-SY5Y differentiation promoted by hsa_circ_0002468. Furthermore, E2F8 was validated as a direct target of miR-561. CONCLUSIONS Our data suggested that hsa_circ_0002468 was a novel circRNA that regulated SH-SY5Y cell proliferation and differentiation via targeting the miR-561/E2F8 axis. Therefore, manipulating hsa_circ_0002468 in SH-SY5Y cells could be a novel strategy to develop novel interventions for the treatment of relevant neurological disorders.</description><identifier>ISSN: 1643-3750</identifier><identifier>ISSN: 1234-1010</identifier><identifier>EISSN: 1643-3750</identifier><identifier>DOI: 10.12659/MSM.915518</identifier><identifier>PMID: 30951518</identifier><language>eng</language><publisher>United States: International Scientific Literature, Inc</publisher><subject>Lab/In Vitro Research</subject><ispartof>Medical science monitor, 2019-04, Vol.25, p.2511-2519</ispartof><rights>Med Sci Monit, 2019 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-d9cb7b5a7eeaa5250121449d5b650b8c62784988175dd7d980e1c619deda8e543</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462173/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462173/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27915,27916,53782,53784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30951518$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Minhui</creatorcontrib><creatorcontrib>Xiang, Guanghong</creatorcontrib><creatorcontrib>Yu, Dan</creatorcontrib><creatorcontrib>Yang, Guoshuai</creatorcontrib><creatorcontrib>He, Weifeng</creatorcontrib><creatorcontrib>Yang, Songlin</creatorcontrib><creatorcontrib>Zhou, Gaoya</creatorcontrib><creatorcontrib>Liu, Aiqun</creatorcontrib><title>Hsa_circ_0002468 Regulates the Neuronal Differentiation of SH-SY5Y Cells by Modulating the MiR-561/E2F8 Axis</title><title>Medical science monitor</title><addtitle>Med Sci Monit</addtitle><description>BACKGROUND It has been shown that circular RNAs (circRNAs) play a vital role in the regulation of neuronal differentiation; however, the precise role of circRNAs in human neuronal differentiation remains largely unexplored. MATERIAL AND METHODS A dual-luciferase reporter assay was carried out to confirm the targets of hsa_circ_0002468, miR-561, E2F8 (E2F transcription factor 8, a protein coding gene), and miR-561. We detected the expression of hsa_circ_0002468, miR-561, and E2F8 by using quantitative real-time polymerase chain reaction (qRT-PCR) analyses. In addition, we performed the functional experiments by using a BrdU (5-bromo-2'-deoxyuridine) assay and qRT-PCR analyses. RESULTS In this study, we showed that hsa_circ_0002468 can act as a sponge of miR-561 to regulate SH-SY5Y proliferation and differentiation. A bioinformatics analysis showed that hsa_circ_0002468 had a binding site that corresponded to miR-561, which was verified by dual-luciferase reporter assay. The expression of hsa_circ_0002468 was increased during SH-SY5Y differentiation and was inversely correlated with miR-561 expression. Using qRT-PCR analysis, we showed that hsa_circ_0002468 negatively regulated miR-561 in SH-SY5Y cells. Intriguingly, the overexpression of hsa_circ_0002468 increased SH-SY5Y differentiation and reduced SH-SY5Y proliferation; the suppression of hsa_circ_0002468 led to decreased SH-SY5Y differentiation levels and increased SH-SY5Y proliferation levels. Additionally, overexpression of miR-561 rescued the SH-SY5Y proliferation deficiency induced by hsa_circ_0002468 overexpression and abolished the SH-SY5Y differentiation promoted by hsa_circ_0002468. Furthermore, E2F8 was validated as a direct target of miR-561. CONCLUSIONS Our data suggested that hsa_circ_0002468 was a novel circRNA that regulated SH-SY5Y cell proliferation and differentiation via targeting the miR-561/E2F8 axis. Therefore, manipulating hsa_circ_0002468 in SH-SY5Y cells could be a novel strategy to develop novel interventions for the treatment of relevant neurological disorders.</description><subject>Lab/In Vitro Research</subject><issn>1643-3750</issn><issn>1234-1010</issn><issn>1643-3750</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVUc1LHDEUD9Ki1nrqveRYkNEkk8-LIKt2BbcFtx48hUzyZo3MTjSZkfrfd3RV7Ok9eL-vxw-hb5QcUiaFOVosF4eGCkH1FtqlktdVrQT59GHfQV9KuSOEaUnENtqpiRF0wu-ibl6c9TF7S6YzlxpfwWrs3AAFD7eAf8GYU-86fBrbFjL0Q3RDTD1OLV7Oq-WNuMEz6LqCmye8SOGZGvvVC3cRryoh6dEZO9f45G8sX9Hn1nUF9l_nHro-P_szm1eXv39ezE4uK8-5GqpgfKMa4RSAc4IJQhnl3ATRSEEa7SVTmhutqRIhqGA0AeolNQGC0yB4vYeON7r3Y7OG4KfU2XX2Pse1y082uWj_v_Tx1q7So5VcMqrqSeDHq0BODyOUwa5j8dObroc0FssY4dIozp-9DjZQn1MpGdp3G0rsSz926sdu-pnQ3z8me8e-FVL_A8MTiUM</recordid><startdate>20190405</startdate><enddate>20190405</enddate><creator>Yang, Minhui</creator><creator>Xiang, Guanghong</creator><creator>Yu, Dan</creator><creator>Yang, Guoshuai</creator><creator>He, Weifeng</creator><creator>Yang, Songlin</creator><creator>Zhou, Gaoya</creator><creator>Liu, Aiqun</creator><general>International Scientific Literature, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190405</creationdate><title>Hsa_circ_0002468 Regulates the Neuronal Differentiation of SH-SY5Y Cells by Modulating the MiR-561/E2F8 Axis</title><author>Yang, Minhui ; Xiang, Guanghong ; Yu, Dan ; Yang, Guoshuai ; He, Weifeng ; Yang, Songlin ; Zhou, Gaoya ; Liu, Aiqun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-d9cb7b5a7eeaa5250121449d5b650b8c62784988175dd7d980e1c619deda8e543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Lab/In Vitro Research</topic><toplevel>online_resources</toplevel><creatorcontrib>Yang, Minhui</creatorcontrib><creatorcontrib>Xiang, Guanghong</creatorcontrib><creatorcontrib>Yu, Dan</creatorcontrib><creatorcontrib>Yang, Guoshuai</creatorcontrib><creatorcontrib>He, Weifeng</creatorcontrib><creatorcontrib>Yang, Songlin</creatorcontrib><creatorcontrib>Zhou, Gaoya</creatorcontrib><creatorcontrib>Liu, Aiqun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medical science monitor</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Minhui</au><au>Xiang, Guanghong</au><au>Yu, Dan</au><au>Yang, Guoshuai</au><au>He, Weifeng</au><au>Yang, Songlin</au><au>Zhou, Gaoya</au><au>Liu, Aiqun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hsa_circ_0002468 Regulates the Neuronal Differentiation of SH-SY5Y Cells by Modulating the MiR-561/E2F8 Axis</atitle><jtitle>Medical science monitor</jtitle><addtitle>Med Sci Monit</addtitle><date>2019-04-05</date><risdate>2019</risdate><volume>25</volume><spage>2511</spage><epage>2519</epage><pages>2511-2519</pages><issn>1643-3750</issn><issn>1234-1010</issn><eissn>1643-3750</eissn><abstract>BACKGROUND It has been shown that circular RNAs (circRNAs) play a vital role in the regulation of neuronal differentiation; however, the precise role of circRNAs in human neuronal differentiation remains largely unexplored. MATERIAL AND METHODS A dual-luciferase reporter assay was carried out to confirm the targets of hsa_circ_0002468, miR-561, E2F8 (E2F transcription factor 8, a protein coding gene), and miR-561. We detected the expression of hsa_circ_0002468, miR-561, and E2F8 by using quantitative real-time polymerase chain reaction (qRT-PCR) analyses. In addition, we performed the functional experiments by using a BrdU (5-bromo-2'-deoxyuridine) assay and qRT-PCR analyses. RESULTS In this study, we showed that hsa_circ_0002468 can act as a sponge of miR-561 to regulate SH-SY5Y proliferation and differentiation. A bioinformatics analysis showed that hsa_circ_0002468 had a binding site that corresponded to miR-561, which was verified by dual-luciferase reporter assay. The expression of hsa_circ_0002468 was increased during SH-SY5Y differentiation and was inversely correlated with miR-561 expression. Using qRT-PCR analysis, we showed that hsa_circ_0002468 negatively regulated miR-561 in SH-SY5Y cells. Intriguingly, the overexpression of hsa_circ_0002468 increased SH-SY5Y differentiation and reduced SH-SY5Y proliferation; the suppression of hsa_circ_0002468 led to decreased SH-SY5Y differentiation levels and increased SH-SY5Y proliferation levels. Additionally, overexpression of miR-561 rescued the SH-SY5Y proliferation deficiency induced by hsa_circ_0002468 overexpression and abolished the SH-SY5Y differentiation promoted by hsa_circ_0002468. Furthermore, E2F8 was validated as a direct target of miR-561. CONCLUSIONS Our data suggested that hsa_circ_0002468 was a novel circRNA that regulated SH-SY5Y cell proliferation and differentiation via targeting the miR-561/E2F8 axis. Therefore, manipulating hsa_circ_0002468 in SH-SY5Y cells could be a novel strategy to develop novel interventions for the treatment of relevant neurological disorders.</abstract><cop>United States</cop><pub>International Scientific Literature, Inc</pub><pmid>30951518</pmid><doi>10.12659/MSM.915518</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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title | Hsa_circ_0002468 Regulates the Neuronal Differentiation of SH-SY5Y Cells by Modulating the MiR-561/E2F8 Axis |
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