Effect of maturation on the expression of aquaporin 3 in mouse oocyte
This study aimed to investigate whether aquaporin 3 (Aqp3) mRNAs are expressed in immature oocytes and altered during in vitro maturation process. Five- to 6-week-old female ICR mice were primed by gonadotropin for 24 and 48 h. Immature oocytes obtained 48 h after priming were also matured in vitro...
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Veröffentlicht in: | Zygote (Cambridge) 2011-02, Vol.19 (1), p.9-14 |
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description | This study aimed to investigate whether aquaporin 3 (Aqp3) mRNAs are expressed in immature oocytes and altered during in vitro maturation process. Five- to 6-week-old female ICR mice were primed by gonadotropin for 24 and 48 h. Immature oocytes obtained 48 h after priming were also matured in vitro for 17 to 18 h. In vivo matured oocytes were obtained after 48 h priming followed by hCG injection. Total RNAs were extracted from 80 to 150 oocytes in each experimental group, and the levels of Aqp3 mRNA were quantified by real-time reverse transcriptase polymerase chain reaction. The experiments were repeated twice using different oocytes. The Aqp3 mRNA was expressed in immature oocytes, as well as in in vitro and in vivo matured oocytes. The expression level was higher in immature oocytes obtained 48 h after priming (17.2 ± 8.6, mean ± SD) than those with no priming (5.7 ± 0.8) or obtained 24 h after priming (2.5 ± 0.8). The expression of Aqp3 mRNA decreased after in vitro maturation (1.2 ± 0.5), which was similar to in vivo matured oocytes (1.0 ± 0.0). Our work demonstrated that Aqp3 mRNA expression increased during the development of immature oocyte but decreased after completion of in vitro maturation. The results indicate that AQP3 is certainly needed for the acquisition of immature oocytes’ full growing potential within antral follicles. |
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Five- to 6-week-old female ICR mice were primed by gonadotropin for 24 and 48 h. Immature oocytes obtained 48 h after priming were also matured in vitro for 17 to 18 h. In vivo matured oocytes were obtained after 48 h priming followed by hCG injection. Total RNAs were extracted from 80 to 150 oocytes in each experimental group, and the levels of Aqp3 mRNA were quantified by real-time reverse transcriptase polymerase chain reaction. The experiments were repeated twice using different oocytes. The Aqp3 mRNA was expressed in immature oocytes, as well as in in vitro and in vivo matured oocytes. The expression level was higher in immature oocytes obtained 48 h after priming (17.2 ± 8.6, mean ± SD) than those with no priming (5.7 ± 0.8) or obtained 24 h after priming (2.5 ± 0.8). The expression of Aqp3 mRNA decreased after in vitro maturation (1.2 ± 0.5), which was similar to in vivo matured oocytes (1.0 ± 0.0). Our work demonstrated that Aqp3 mRNA expression increased during the development of immature oocyte but decreased after completion of in vitro maturation. The results indicate that AQP3 is certainly needed for the acquisition of immature oocytes’ full growing potential within antral follicles.</description><identifier>ISSN: 0967-1994</identifier><identifier>EISSN: 1469-8730</identifier><identifier>DOI: 10.1017/S0967199410000171</identifier><identifier>PMID: 20509986</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Animals ; Aquaporin 3 - genetics ; Aquaporin 3 - metabolism ; Female ; Mice ; Mice, Inbred ICR ; Oocytes - cytology ; Oocytes - metabolism ; Ovarian Follicle - drug effects ; Ovarian Follicle - metabolism ; RNA, Messenger - metabolism</subject><ispartof>Zygote (Cambridge), 2011-02, Vol.19 (1), p.9-14</ispartof><rights>Copyright © Cambridge University Press 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-e2b26ea00994a8e79d6cb2dd074a021ad7cf44c42eaf38b58efe2c260ff2e6873</citedby><cites>FETCH-LOGICAL-c371t-e2b26ea00994a8e79d6cb2dd074a021ad7cf44c42eaf38b58efe2c260ff2e6873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0967199410000171/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>164,314,776,780,27901,27902,55603</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20509986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jo, Jun Woo</creatorcontrib><creatorcontrib>Jee, Byung Chul</creatorcontrib><creatorcontrib>Suh, Chang Suk</creatorcontrib><creatorcontrib>Kim, Seok Hyun</creatorcontrib><creatorcontrib>Choi, Young Min</creatorcontrib><creatorcontrib>Kim, Jung Gu</creatorcontrib><creatorcontrib>Moon, Shin Yong</creatorcontrib><title>Effect of maturation on the expression of aquaporin 3 in mouse oocyte</title><title>Zygote (Cambridge)</title><addtitle>Zygote</addtitle><description>This study aimed to investigate whether aquaporin 3 (Aqp3) mRNAs are expressed in immature oocytes and altered during in vitro maturation process. Five- to 6-week-old female ICR mice were primed by gonadotropin for 24 and 48 h. Immature oocytes obtained 48 h after priming were also matured in vitro for 17 to 18 h. In vivo matured oocytes were obtained after 48 h priming followed by hCG injection. Total RNAs were extracted from 80 to 150 oocytes in each experimental group, and the levels of Aqp3 mRNA were quantified by real-time reverse transcriptase polymerase chain reaction. The experiments were repeated twice using different oocytes. The Aqp3 mRNA was expressed in immature oocytes, as well as in in vitro and in vivo matured oocytes. The expression level was higher in immature oocytes obtained 48 h after priming (17.2 ± 8.6, mean ± SD) than those with no priming (5.7 ± 0.8) or obtained 24 h after priming (2.5 ± 0.8). The expression of Aqp3 mRNA decreased after in vitro maturation (1.2 ± 0.5), which was similar to in vivo matured oocytes (1.0 ± 0.0). Our work demonstrated that Aqp3 mRNA expression increased during the development of immature oocyte but decreased after completion of in vitro maturation. The results indicate that AQP3 is certainly needed for the acquisition of immature oocytes’ full growing potential within antral follicles.</description><subject>Animals</subject><subject>Aquaporin 3 - genetics</subject><subject>Aquaporin 3 - metabolism</subject><subject>Female</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Oocytes - cytology</subject><subject>Oocytes - metabolism</subject><subject>Ovarian Follicle - drug effects</subject><subject>Ovarian Follicle - metabolism</subject><subject>RNA, Messenger - metabolism</subject><issn>0967-1994</issn><issn>1469-8730</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kE1LAzEQhoMotlZ_gBcJXjytJtk0H0cp9QMED-p5yWYnuqW72Sa7YP-9qa0KimFIIPPMOzMvQqeUXFJC5dUT0UJSrTkl6VBJ99CYcqEzJXOyj8abdLbJj9BRjIvESKn5IRoxMiVaKzFG87lzYHvsHW5MPwTT177FKfo3wPDeBYjx88dhsxpM50Pd4hynq_FDBOy9XfdwjA6cWUY42b0T9HIzf57dZQ-Pt_ez64fM5pL2GbCSCTAk9eZGgdSVsCWrKiK5IYyaSlrHueUMjMtVOVXggFkmiHMMRFpqgi62ul3wqwFiXzR1tLBcmhbSOIViTJNcT2kiz3-RCz-ENg1XKE4Ek0SxBNEtZIOPMYArulA3JqwLSoqNw8Ufh1PN2U54KBuoviu-LE1AvhM1TRnq6hV-Wv8v-wFdjISP</recordid><startdate>201102</startdate><enddate>201102</enddate><creator>Jo, Jun Woo</creator><creator>Jee, Byung Chul</creator><creator>Suh, Chang Suk</creator><creator>Kim, Seok Hyun</creator><creator>Choi, Young Min</creator><creator>Kim, Jung Gu</creator><creator>Moon, Shin Yong</creator><general>Cambridge University Press</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>3V.</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>201102</creationdate><title>Effect of maturation on the expression of aquaporin 3 in mouse oocyte</title><author>Jo, Jun Woo ; Jee, Byung Chul ; Suh, Chang Suk ; Kim, Seok Hyun ; Choi, Young Min ; Kim, Jung Gu ; Moon, Shin Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-e2b26ea00994a8e79d6cb2dd074a021ad7cf44c42eaf38b58efe2c260ff2e6873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Aquaporin 3 - genetics</topic><topic>Aquaporin 3 - metabolism</topic><topic>Female</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Oocytes - cytology</topic><topic>Oocytes - metabolism</topic><topic>Ovarian Follicle - drug effects</topic><topic>Ovarian Follicle - metabolism</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jo, Jun Woo</creatorcontrib><creatorcontrib>Jee, Byung Chul</creatorcontrib><creatorcontrib>Suh, Chang Suk</creatorcontrib><creatorcontrib>Kim, Seok Hyun</creatorcontrib><creatorcontrib>Choi, Young Min</creatorcontrib><creatorcontrib>Kim, Jung Gu</creatorcontrib><creatorcontrib>Moon, Shin Yong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Zygote (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jo, Jun Woo</au><au>Jee, Byung Chul</au><au>Suh, Chang Suk</au><au>Kim, Seok Hyun</au><au>Choi, Young Min</au><au>Kim, Jung Gu</au><au>Moon, Shin Yong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of maturation on the expression of aquaporin 3 in mouse oocyte</atitle><jtitle>Zygote (Cambridge)</jtitle><addtitle>Zygote</addtitle><date>2011-02</date><risdate>2011</risdate><volume>19</volume><issue>1</issue><spage>9</spage><epage>14</epage><pages>9-14</pages><issn>0967-1994</issn><eissn>1469-8730</eissn><abstract>This study aimed to investigate whether aquaporin 3 (Aqp3) mRNAs are expressed in immature oocytes and altered during in vitro maturation process. Five- to 6-week-old female ICR mice were primed by gonadotropin for 24 and 48 h. Immature oocytes obtained 48 h after priming were also matured in vitro for 17 to 18 h. In vivo matured oocytes were obtained after 48 h priming followed by hCG injection. Total RNAs were extracted from 80 to 150 oocytes in each experimental group, and the levels of Aqp3 mRNA were quantified by real-time reverse transcriptase polymerase chain reaction. The experiments were repeated twice using different oocytes. The Aqp3 mRNA was expressed in immature oocytes, as well as in in vitro and in vivo matured oocytes. The expression level was higher in immature oocytes obtained 48 h after priming (17.2 ± 8.6, mean ± SD) than those with no priming (5.7 ± 0.8) or obtained 24 h after priming (2.5 ± 0.8). The expression of Aqp3 mRNA decreased after in vitro maturation (1.2 ± 0.5), which was similar to in vivo matured oocytes (1.0 ± 0.0). Our work demonstrated that Aqp3 mRNA expression increased during the development of immature oocyte but decreased after completion of in vitro maturation. The results indicate that AQP3 is certainly needed for the acquisition of immature oocytes’ full growing potential within antral follicles.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>20509986</pmid><doi>10.1017/S0967199410000171</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Aquaporin 3 - genetics Aquaporin 3 - metabolism Female Mice Mice, Inbred ICR Oocytes - cytology Oocytes - metabolism Ovarian Follicle - drug effects Ovarian Follicle - metabolism RNA, Messenger - metabolism |
title | Effect of maturation on the expression of aquaporin 3 in mouse oocyte |
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