Induction of right open reading frame kinase 3 (RIOK3) during ovulation and luteinisation in rat ovary
Atypical protein serine kinase RIOK3 is involved in cellular invasion and survival. The spatiotemporal expression pattern and regulatory mechanisms controlling expression of Riok3 were investigated in the rat ovary during the periovulatory period. Immature female rats (22-23 days old) were treated w...
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Veröffentlicht in: | Reproduction fertility and development 2021-11, Vol.33 (16), p.810-816 |
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creator | Zhang, Wei Zhang, Chujing Huang, Ruiqi Qiu, Mengsheng Li, Fei-Xue |
description | Atypical protein serine kinase RIOK3 is involved in cellular invasion and survival. The spatiotemporal expression pattern and regulatory mechanisms controlling expression of Riok3 were investigated in the rat ovary during the periovulatory period. Immature female rats (22-23 days old) were treated with pregnant mare's serum gonadotropin (PMSG) to stimulate follicular development, followed 48h later by injection with human chorionic gonadotrophin (hCG). Ovaries, granulosa cells, or theca-interstitial cells were collected at various times after hCG administration. Both real-time polymerase chain reaction (PCR) and in situ hybridisation analysis revealed that Riok3 was highly induced in both granulosa cells and theca-interstitial cells by hCG. Riok3 expression was induced in theca-interstitial cells at 4h after hCG. However, the expression of Riok3 mRNA was stimulated in granulosa cells at 8h. Both protein kinase C inhibitor (GF109203) and the protein kinase A inhibitor (H89) could block the stimulation of Riok3 mRNA by hCG. Furthermore, Riok3 induction is dependent on new protein synthesis. Inhibition of prostaglandin synthesis or progesterone action did not alter Riok3 mRNA expression, whereas inhibition of the epidermal growth factor (EGF) pathway downregulated Riok3 expression. In conclusion, our findings suggest that the induction of the RIOK3 may be important for ovulation and luteinisation. |
doi_str_mv | 10.1071/RD21118 |
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The spatiotemporal expression pattern and regulatory mechanisms controlling expression of Riok3 were investigated in the rat ovary during the periovulatory period. Immature female rats (22-23 days old) were treated with pregnant mare's serum gonadotropin (PMSG) to stimulate follicular development, followed 48h later by injection with human chorionic gonadotrophin (hCG). Ovaries, granulosa cells, or theca-interstitial cells were collected at various times after hCG administration. Both real-time polymerase chain reaction (PCR) and in situ hybridisation analysis revealed that Riok3 was highly induced in both granulosa cells and theca-interstitial cells by hCG. Riok3 expression was induced in theca-interstitial cells at 4h after hCG. However, the expression of Riok3 mRNA was stimulated in granulosa cells at 8h. Both protein kinase C inhibitor (GF109203) and the protein kinase A inhibitor (H89) could block the stimulation of Riok3 mRNA by hCG. Furthermore, Riok3 induction is dependent on new protein synthesis. Inhibition of prostaglandin synthesis or progesterone action did not alter Riok3 mRNA expression, whereas inhibition of the epidermal growth factor (EGF) pathway downregulated Riok3 expression. In conclusion, our findings suggest that the induction of the RIOK3 may be important for ovulation and luteinisation.</description><identifier>ISSN: 1031-3613</identifier><identifier>EISSN: 1448-5990</identifier><identifier>DOI: 10.1071/RD21118</identifier><identifier>PMID: 34758896</identifier><language>eng</language><publisher>Australia</publisher><subject>Animals ; Female ; Gonadotropins, Equine - pharmacology ; Granulosa Cells - drug effects ; Granulosa Cells - metabolism ; Luteinization - drug effects ; Luteinization - genetics ; Luteinization - metabolism ; Ovary - drug effects ; Ovary - metabolism ; Ovulation - drug effects ; Ovulation - genetics ; Ovulation - metabolism ; Protein Serine-Threonine Kinases - genetics ; Protein Serine-Threonine Kinases - metabolism ; Rats ; Signal Transduction - drug effects</subject><ispartof>Reproduction fertility and development, 2021-11, Vol.33 (16), p.810-816</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c243t-8b1d37f116dee2d86cb4db6eee46f6dd700d5dd23cfd562b2951d450438fb7f3</cites><orcidid>0000-0001-5566-3125</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34758896$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Zhang, Chujing</creatorcontrib><creatorcontrib>Huang, Ruiqi</creatorcontrib><creatorcontrib>Qiu, Mengsheng</creatorcontrib><creatorcontrib>Li, Fei-Xue</creatorcontrib><title>Induction of right open reading frame kinase 3 (RIOK3) during ovulation and luteinisation in rat ovary</title><title>Reproduction fertility and development</title><addtitle>Reprod Fertil Dev</addtitle><description>Atypical protein serine kinase RIOK3 is involved in cellular invasion and survival. The spatiotemporal expression pattern and regulatory mechanisms controlling expression of Riok3 were investigated in the rat ovary during the periovulatory period. Immature female rats (22-23 days old) were treated with pregnant mare's serum gonadotropin (PMSG) to stimulate follicular development, followed 48h later by injection with human chorionic gonadotrophin (hCG). Ovaries, granulosa cells, or theca-interstitial cells were collected at various times after hCG administration. Both real-time polymerase chain reaction (PCR) and in situ hybridisation analysis revealed that Riok3 was highly induced in both granulosa cells and theca-interstitial cells by hCG. Riok3 expression was induced in theca-interstitial cells at 4h after hCG. However, the expression of Riok3 mRNA was stimulated in granulosa cells at 8h. Both protein kinase C inhibitor (GF109203) and the protein kinase A inhibitor (H89) could block the stimulation of Riok3 mRNA by hCG. Furthermore, Riok3 induction is dependent on new protein synthesis. Inhibition of prostaglandin synthesis or progesterone action did not alter Riok3 mRNA expression, whereas inhibition of the epidermal growth factor (EGF) pathway downregulated Riok3 expression. In conclusion, our findings suggest that the induction of the RIOK3 may be important for ovulation and luteinisation.</description><subject>Animals</subject><subject>Female</subject><subject>Gonadotropins, Equine - pharmacology</subject><subject>Granulosa Cells - drug effects</subject><subject>Granulosa Cells - metabolism</subject><subject>Luteinization - drug effects</subject><subject>Luteinization - genetics</subject><subject>Luteinization - metabolism</subject><subject>Ovary - drug effects</subject><subject>Ovary - metabolism</subject><subject>Ovulation - drug effects</subject><subject>Ovulation - genetics</subject><subject>Ovulation - metabolism</subject><subject>Protein Serine-Threonine Kinases - genetics</subject><subject>Protein Serine-Threonine Kinases - metabolism</subject><subject>Rats</subject><subject>Signal Transduction - drug effects</subject><issn>1031-3613</issn><issn>1448-5990</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMtOwzAQRS0EolAQf4C8oywCfsdZovKqqFSp6j5y4nEx5FHspBJ_T0oLqxnNnDkaXYSuKLmjJKX3y0dGKdVH6IwKoROZZeR46AmnCVeUj9B5jB-EUKEYP0UjLlKpdabOkJs1ti873za4dTj49XuH2w00OICxvlljF0wN-NM3JgLmeLKcLd74LbZ92G3bbV-Z32vTWFz1HfjGx_3EDxIz2LYmfF-gE2eqCJeHOkar56fV9DWZL15m04d5UjLBu0QX1PLUUaosALNalYWwhQIAoZyyNiXESmsZL52VihUsk9QKSQTXrkgdH6PJXrsJ7VcPsctrH0uoKtNA28ecyUwJKbTMBvRmj5ahjTGAyzfB18OrOSX5LtP8kOlAXh-kfVGD_ef-QuQ_6sNxRg</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Zhang, Wei</creator><creator>Zhang, Chujing</creator><creator>Huang, Ruiqi</creator><creator>Qiu, Mengsheng</creator><creator>Li, Fei-Xue</creator><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>7X8</scope><orcidid>https://orcid.org/0000-0001-5566-3125</orcidid></search><sort><creationdate>20211101</creationdate><title>Induction of right open reading frame kinase 3 (RIOK3) during ovulation and luteinisation in rat ovary</title><author>Zhang, Wei ; Zhang, Chujing ; Huang, Ruiqi ; Qiu, Mengsheng ; Li, Fei-Xue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c243t-8b1d37f116dee2d86cb4db6eee46f6dd700d5dd23cfd562b2951d450438fb7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Female</topic><topic>Gonadotropins, Equine - pharmacology</topic><topic>Granulosa Cells - drug effects</topic><topic>Granulosa Cells - metabolism</topic><topic>Luteinization - drug effects</topic><topic>Luteinization - genetics</topic><topic>Luteinization - metabolism</topic><topic>Ovary - drug effects</topic><topic>Ovary - metabolism</topic><topic>Ovulation - drug effects</topic><topic>Ovulation - genetics</topic><topic>Ovulation - metabolism</topic><topic>Protein Serine-Threonine Kinases - genetics</topic><topic>Protein Serine-Threonine Kinases - metabolism</topic><topic>Rats</topic><topic>Signal Transduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Zhang, Chujing</creatorcontrib><creatorcontrib>Huang, Ruiqi</creatorcontrib><creatorcontrib>Qiu, Mengsheng</creatorcontrib><creatorcontrib>Li, Fei-Xue</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Reproduction fertility and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Wei</au><au>Zhang, Chujing</au><au>Huang, Ruiqi</au><au>Qiu, Mengsheng</au><au>Li, Fei-Xue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of right open reading frame kinase 3 (RIOK3) during ovulation and luteinisation in rat ovary</atitle><jtitle>Reproduction fertility and development</jtitle><addtitle>Reprod Fertil Dev</addtitle><date>2021-11-01</date><risdate>2021</risdate><volume>33</volume><issue>16</issue><spage>810</spage><epage>816</epage><pages>810-816</pages><issn>1031-3613</issn><eissn>1448-5990</eissn><abstract>Atypical protein serine kinase RIOK3 is involved in cellular invasion and survival. The spatiotemporal expression pattern and regulatory mechanisms controlling expression of Riok3 were investigated in the rat ovary during the periovulatory period. Immature female rats (22-23 days old) were treated with pregnant mare's serum gonadotropin (PMSG) to stimulate follicular development, followed 48h later by injection with human chorionic gonadotrophin (hCG). Ovaries, granulosa cells, or theca-interstitial cells were collected at various times after hCG administration. Both real-time polymerase chain reaction (PCR) and in situ hybridisation analysis revealed that Riok3 was highly induced in both granulosa cells and theca-interstitial cells by hCG. Riok3 expression was induced in theca-interstitial cells at 4h after hCG. However, the expression of Riok3 mRNA was stimulated in granulosa cells at 8h. Both protein kinase C inhibitor (GF109203) and the protein kinase A inhibitor (H89) could block the stimulation of Riok3 mRNA by hCG. Furthermore, Riok3 induction is dependent on new protein synthesis. Inhibition of prostaglandin synthesis or progesterone action did not alter Riok3 mRNA expression, whereas inhibition of the epidermal growth factor (EGF) pathway downregulated Riok3 expression. In conclusion, our findings suggest that the induction of the RIOK3 may be important for ovulation and luteinisation.</abstract><cop>Australia</cop><pmid>34758896</pmid><doi>10.1071/RD21118</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-5566-3125</orcidid></addata></record> |
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subjects | Animals Female Gonadotropins, Equine - pharmacology Granulosa Cells - drug effects Granulosa Cells - metabolism Luteinization - drug effects Luteinization - genetics Luteinization - metabolism Ovary - drug effects Ovary - metabolism Ovulation - drug effects Ovulation - genetics Ovulation - metabolism Protein Serine-Threonine Kinases - genetics Protein Serine-Threonine Kinases - metabolism Rats Signal Transduction - drug effects |
title | Induction of right open reading frame kinase 3 (RIOK3) during ovulation and luteinisation in rat ovary |
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