Hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells of marine medaka Oryzias melastigma
•We demonstrate hypoxia induced miR-210 in ovarian follicular cells.•We show anti-apoptotic roles of miR-210 in ovarian follicular cells under hypoxia.•Apoptotic genes (DLC1, SLK, TNFRSF10B, RBM25, and USP7) are target of miR-210.•MiR-210 is vital for ovarian follicular cells proliferation in respon...
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creator | Tse, Anna Chung-Kwan Li, Jing-Woei Chan, Ting-Fung Wu, Rudolf Shiu-Sun Lai, Keng-Po |
description | •We demonstrate hypoxia induced miR-210 in ovarian follicular cells.•We show anti-apoptotic roles of miR-210 in ovarian follicular cells under hypoxia.•Apoptotic genes (DLC1, SLK, TNFRSF10B, RBM25, and USP7) are target of miR-210.•MiR-210 is vital for ovarian follicular cells proliferation in response to hypoxia.
Hypoxia is a major global problem that impairs reproductive functions and reduces the quality and quantity of gametes and the fertilization success of marine fish. Nevertheless, the detailed molecular mechanism underlying hypoxia-induced female reproductive impairment remains largely unknown. There is increasing evidence that miRNA is vital in regulating ovarian functions and is closely associated with female fertility in humans. Certain miRNAs that regulate apoptotic genes can be induced by hypoxia, resulting in cell apoptosis. Using primary ovarian follicular cells of the marine medaka, Oryzias melastigma, as a model, we investigated the response of miR-210 to hypoxic stress in ovarian tissues to see if it would interrupt reproductive functions. A significant induction of miR-210 was found in primary ovarian follicular cells exposed to hypoxia, and gene ontology analysis further highlighted the potential roles of miR-210 in cell proliferation, cell differentiation, and cell apoptosis. A number of miR-210 target apoptotic genes, including Deleted in liver cancer 1 protein (DLC1), STE20-like serine/threonine-protein kinase (SLK), tumor necrosis factor receptor superfamily member 10b (TNFRSF10B), RNA binding motif protein 25 (RBM25), and Ubiquitin-specific-processing protease 7 (USP7), were identified. We further showed that ectopic expression of miR-210 would result in down-regulation of these apoptotic genes. On the other hand, the inhibition of miR-210 promoted apoptotic cell death and the expression of apoptotic marker – caspase 3 in follicular cells under hypoxic treatment, supporting the regulatory role of miR-210 in ovarian cell apoptosis. This study provides new insights on how hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells in fish, which is fundamentally important in environmental sciences and reproductive biology. |
doi_str_mv | 10.1016/j.aquatox.2015.06.002 |
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Hypoxia is a major global problem that impairs reproductive functions and reduces the quality and quantity of gametes and the fertilization success of marine fish. Nevertheless, the detailed molecular mechanism underlying hypoxia-induced female reproductive impairment remains largely unknown. There is increasing evidence that miRNA is vital in regulating ovarian functions and is closely associated with female fertility in humans. Certain miRNAs that regulate apoptotic genes can be induced by hypoxia, resulting in cell apoptosis. Using primary ovarian follicular cells of the marine medaka, Oryzias melastigma, as a model, we investigated the response of miR-210 to hypoxic stress in ovarian tissues to see if it would interrupt reproductive functions. A significant induction of miR-210 was found in primary ovarian follicular cells exposed to hypoxia, and gene ontology analysis further highlighted the potential roles of miR-210 in cell proliferation, cell differentiation, and cell apoptosis. A number of miR-210 target apoptotic genes, including Deleted in liver cancer 1 protein (DLC1), STE20-like serine/threonine-protein kinase (SLK), tumor necrosis factor receptor superfamily member 10b (TNFRSF10B), RNA binding motif protein 25 (RBM25), and Ubiquitin-specific-processing protease 7 (USP7), were identified. We further showed that ectopic expression of miR-210 would result in down-regulation of these apoptotic genes. On the other hand, the inhibition of miR-210 promoted apoptotic cell death and the expression of apoptotic marker – caspase 3 in follicular cells under hypoxic treatment, supporting the regulatory role of miR-210 in ovarian cell apoptosis. This study provides new insights on how hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells in fish, which is fundamentally important in environmental sciences and reproductive biology.</description><identifier>ISSN: 0166-445X</identifier><identifier>EISSN: 1879-1514</identifier><identifier>DOI: 10.1016/j.aquatox.2015.06.002</identifier><identifier>PMID: 26074452</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Apoptosis ; Apoptosis - genetics ; Apoptosis - physiology ; Cell Proliferation - genetics ; Down-Regulation - physiology ; Female ; Freshwater ; Hypoxia ; Hypoxia - physiopathology ; Marine medaka ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Mirna ; Oryzias - genetics ; Oryzias - metabolism ; Oryzias - physiology ; Oryzias latipes ; Oryzias melastigma ; Ovarian Follicle - enzymology ; Ovarian Follicle - physiopathology ; Ovarian follicular cells ; Stress, Physiological - genetics</subject><ispartof>Aquatic toxicology, 2015-08, Vol.165, p.189-196</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-cebff24c4f3055a170f2d46da601b1b401dd0e081e42b2d5cae83073ab3d27603</citedby><cites>FETCH-LOGICAL-c464t-cebff24c4f3055a170f2d46da601b1b401dd0e081e42b2d5cae83073ab3d27603</cites><orcidid>0000-0002-0489-3884</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0166445X15001745$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26074452$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tse, Anna Chung-Kwan</creatorcontrib><creatorcontrib>Li, Jing-Woei</creatorcontrib><creatorcontrib>Chan, Ting-Fung</creatorcontrib><creatorcontrib>Wu, Rudolf Shiu-Sun</creatorcontrib><creatorcontrib>Lai, Keng-Po</creatorcontrib><title>Hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells of marine medaka Oryzias melastigma</title><title>Aquatic toxicology</title><addtitle>Aquat Toxicol</addtitle><description>•We demonstrate hypoxia induced miR-210 in ovarian follicular cells.•We show anti-apoptotic roles of miR-210 in ovarian follicular cells under hypoxia.•Apoptotic genes (DLC1, SLK, TNFRSF10B, RBM25, and USP7) are target of miR-210.•MiR-210 is vital for ovarian follicular cells proliferation in response to hypoxia.
Hypoxia is a major global problem that impairs reproductive functions and reduces the quality and quantity of gametes and the fertilization success of marine fish. Nevertheless, the detailed molecular mechanism underlying hypoxia-induced female reproductive impairment remains largely unknown. There is increasing evidence that miRNA is vital in regulating ovarian functions and is closely associated with female fertility in humans. Certain miRNAs that regulate apoptotic genes can be induced by hypoxia, resulting in cell apoptosis. Using primary ovarian follicular cells of the marine medaka, Oryzias melastigma, as a model, we investigated the response of miR-210 to hypoxic stress in ovarian tissues to see if it would interrupt reproductive functions. A significant induction of miR-210 was found in primary ovarian follicular cells exposed to hypoxia, and gene ontology analysis further highlighted the potential roles of miR-210 in cell proliferation, cell differentiation, and cell apoptosis. A number of miR-210 target apoptotic genes, including Deleted in liver cancer 1 protein (DLC1), STE20-like serine/threonine-protein kinase (SLK), tumor necrosis factor receptor superfamily member 10b (TNFRSF10B), RNA binding motif protein 25 (RBM25), and Ubiquitin-specific-processing protease 7 (USP7), were identified. We further showed that ectopic expression of miR-210 would result in down-regulation of these apoptotic genes. On the other hand, the inhibition of miR-210 promoted apoptotic cell death and the expression of apoptotic marker – caspase 3 in follicular cells under hypoxic treatment, supporting the regulatory role of miR-210 in ovarian cell apoptosis. This study provides new insights on how hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells in fish, which is fundamentally important in environmental sciences and reproductive biology.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - genetics</subject><subject>Apoptosis - physiology</subject><subject>Cell Proliferation - genetics</subject><subject>Down-Regulation - physiology</subject><subject>Female</subject><subject>Freshwater</subject><subject>Hypoxia</subject><subject>Hypoxia - physiopathology</subject><subject>Marine medaka</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Mirna</subject><subject>Oryzias - genetics</subject><subject>Oryzias - metabolism</subject><subject>Oryzias - physiology</subject><subject>Oryzias latipes</subject><subject>Oryzias melastigma</subject><subject>Ovarian Follicle - enzymology</subject><subject>Ovarian Follicle - physiopathology</subject><subject>Ovarian follicular cells</subject><subject>Stress, Physiological - genetics</subject><issn>0166-445X</issn><issn>1879-1514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1q3DAURkVpaKZpH6FByy5q50qW5ZlVCKFtCoFAaKE7cS1dB01ty5HskMnTV8NMuq02Auncn-8w9klAKUDoi22JjwvO4bmUIOoSdAkg37CVWDebQtRCvWWrzOlCqfr3KXuf0hbykWrzjp1KDU1-lysWb3ZTePbI_egWS4kP_r6QAr7wntD58YHPgeM4-wKnMM0h-ZRRHp4wehx5F_re26XHyC31feKh40P-GokP5PAP8ru4e_GY-1KPafYPA35gJx32iT4e7zP269vXn9c3xe3d9x_XV7eFVVrNhaW266SyqqugrlE00EmntEMNohWtAuEcEKwFKdlKV1ukdQVNhW3lZKOhOmOfD32nGB4XSrMZfNpviSOFJRnRVPVGKiWrjNYH1MaQUqTOTNHnHDsjwOx1m6056jZ73Qa0yS5z3flxxNLmvP-qXv1m4PIAUA765CmaZD2NlpyPZGfjgv_PiL-czJUI</recordid><startdate>201508</startdate><enddate>201508</enddate><creator>Tse, Anna Chung-Kwan</creator><creator>Li, Jing-Woei</creator><creator>Chan, Ting-Fung</creator><creator>Wu, Rudolf Shiu-Sun</creator><creator>Lai, Keng-Po</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QH</scope><scope>7ST</scope><scope>7TN</scope><scope>7U7</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0002-0489-3884</orcidid></search><sort><creationdate>201508</creationdate><title>Hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells of marine medaka Oryzias melastigma</title><author>Tse, Anna Chung-Kwan ; Li, Jing-Woei ; Chan, Ting-Fung ; Wu, Rudolf Shiu-Sun ; Lai, Keng-Po</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-cebff24c4f3055a170f2d46da601b1b401dd0e081e42b2d5cae83073ab3d27603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - genetics</topic><topic>Apoptosis - physiology</topic><topic>Cell Proliferation - genetics</topic><topic>Down-Regulation - physiology</topic><topic>Female</topic><topic>Freshwater</topic><topic>Hypoxia</topic><topic>Hypoxia - physiopathology</topic><topic>Marine medaka</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Mirna</topic><topic>Oryzias - genetics</topic><topic>Oryzias - metabolism</topic><topic>Oryzias - physiology</topic><topic>Oryzias latipes</topic><topic>Oryzias melastigma</topic><topic>Ovarian Follicle - enzymology</topic><topic>Ovarian Follicle - physiopathology</topic><topic>Ovarian follicular cells</topic><topic>Stress, Physiological - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tse, Anna Chung-Kwan</creatorcontrib><creatorcontrib>Li, Jing-Woei</creatorcontrib><creatorcontrib>Chan, Ting-Fung</creatorcontrib><creatorcontrib>Wu, Rudolf Shiu-Sun</creatorcontrib><creatorcontrib>Lai, Keng-Po</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Environment Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Environment Abstracts</collection><jtitle>Aquatic toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tse, Anna Chung-Kwan</au><au>Li, Jing-Woei</au><au>Chan, Ting-Fung</au><au>Wu, Rudolf Shiu-Sun</au><au>Lai, Keng-Po</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells of marine medaka Oryzias melastigma</atitle><jtitle>Aquatic toxicology</jtitle><addtitle>Aquat Toxicol</addtitle><date>2015-08</date><risdate>2015</risdate><volume>165</volume><spage>189</spage><epage>196</epage><pages>189-196</pages><issn>0166-445X</issn><eissn>1879-1514</eissn><abstract>•We demonstrate hypoxia induced miR-210 in ovarian follicular cells.•We show anti-apoptotic roles of miR-210 in ovarian follicular cells under hypoxia.•Apoptotic genes (DLC1, SLK, TNFRSF10B, RBM25, and USP7) are target of miR-210.•MiR-210 is vital for ovarian follicular cells proliferation in response to hypoxia.
Hypoxia is a major global problem that impairs reproductive functions and reduces the quality and quantity of gametes and the fertilization success of marine fish. Nevertheless, the detailed molecular mechanism underlying hypoxia-induced female reproductive impairment remains largely unknown. There is increasing evidence that miRNA is vital in regulating ovarian functions and is closely associated with female fertility in humans. Certain miRNAs that regulate apoptotic genes can be induced by hypoxia, resulting in cell apoptosis. Using primary ovarian follicular cells of the marine medaka, Oryzias melastigma, as a model, we investigated the response of miR-210 to hypoxic stress in ovarian tissues to see if it would interrupt reproductive functions. A significant induction of miR-210 was found in primary ovarian follicular cells exposed to hypoxia, and gene ontology analysis further highlighted the potential roles of miR-210 in cell proliferation, cell differentiation, and cell apoptosis. A number of miR-210 target apoptotic genes, including Deleted in liver cancer 1 protein (DLC1), STE20-like serine/threonine-protein kinase (SLK), tumor necrosis factor receptor superfamily member 10b (TNFRSF10B), RNA binding motif protein 25 (RBM25), and Ubiquitin-specific-processing protease 7 (USP7), were identified. We further showed that ectopic expression of miR-210 would result in down-regulation of these apoptotic genes. On the other hand, the inhibition of miR-210 promoted apoptotic cell death and the expression of apoptotic marker – caspase 3 in follicular cells under hypoxic treatment, supporting the regulatory role of miR-210 in ovarian cell apoptosis. This study provides new insights on how hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells in fish, which is fundamentally important in environmental sciences and reproductive biology.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26074452</pmid><doi>10.1016/j.aquatox.2015.06.002</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0489-3884</orcidid></addata></record> |
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subjects | Animals Apoptosis Apoptosis - genetics Apoptosis - physiology Cell Proliferation - genetics Down-Regulation - physiology Female Freshwater Hypoxia Hypoxia - physiopathology Marine medaka MicroRNAs - genetics MicroRNAs - metabolism Mirna Oryzias - genetics Oryzias - metabolism Oryzias - physiology Oryzias latipes Oryzias melastigma Ovarian Follicle - enzymology Ovarian Follicle - physiopathology Ovarian follicular cells Stress, Physiological - genetics |
title | Hypoxia induces miR-210, leading to anti-apoptosis in ovarian follicular cells of marine medaka Oryzias melastigma |
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