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Nuclear and cytoplasmic maturation of in vitro matured human oocytes after temporary nuclear arrest by phosphodiesterase 3-inhibitor

BACKGROUND The use of hormones for controlled ovarian stimulation results in follicular heterogeneity, with oocytes at diverse stages of nuclear and cytoplasmic development. This study evaluated the impact of temporary nuclear arrest by a specific phosphodiesterase 3-inhibitor (PDE3-I), cilostamide,...

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Published in:Human reproduction (Oxford) 2007-05, Vol.22 (5), p.1239-1246
Main Authors: Vanhoutte, Leen, De Sutter, Petra, Nogueira, Daniela, Gerris, Jan, Dhont, Marc, Van der Elst, Josiane
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cited_by cdi_FETCH-LOGICAL-c486t-e77eb5ac2258b3e9803ae451d059bd8390f8e0a8cd591c38f382336ff7643e7d3
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container_issue 5
container_start_page 1239
container_title Human reproduction (Oxford)
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creator Vanhoutte, Leen
De Sutter, Petra
Nogueira, Daniela
Gerris, Jan
Dhont, Marc
Van der Elst, Josiane
description BACKGROUND The use of hormones for controlled ovarian stimulation results in follicular heterogeneity, with oocytes at diverse stages of nuclear and cytoplasmic development. This study evaluated the impact of temporary nuclear arrest by a specific phosphodiesterase 3-inhibitor (PDE3-I), cilostamide, on nuclear and cytoplasmic maturation of cumulus-free germinal vesicle (GV) human oocytes from controlled ovarian stimulated cycles. METHODS GV oocytes (n = 234) were cultured in: (i) medium without the inhibitor (control); (ii) medium supplemented with 1 µM cilostamide and (iii) medium supplemented with 10 µM cilostamide. Oocytes in groups (ii) and (iii) were exposed to cilostamide for 24 h. The PDE3-I was subsequently removed by transfer of oocytes to fresh in vitro maturation (IVM) medium and the reversibility of GV arrest was assessed during IVM culture for maximum 48 h. RESULTS Cilostamide (1 and 10 µM) could maintain >80% of the oocytes at the GV stage, without affecting subsequent maturation to metaphase II. Oocytes exposed to 1 µM cilostamide were more likely to have normal bipolar spindles with aligned chromosomes than control oocytes (P < 0.05). When GV chromatin configurations before and after arrest were compared, a significantly higher proportion of oocytes had acquired a nucleolus completely surrounded by a rim of highly condensed chromatin (P < 0.05). CONCLUSIONS Temporary nuclear arrest of human GV oocytes with PDE3-I proved to be beneficial for obtaining normal spindle and chromosome configurations after IVM. It resulted also in synchronization within the population of GV oocytes.
doi_str_mv 10.1093/humrep/dem007
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This study evaluated the impact of temporary nuclear arrest by a specific phosphodiesterase 3-inhibitor (PDE3-I), cilostamide, on nuclear and cytoplasmic maturation of cumulus-free germinal vesicle (GV) human oocytes from controlled ovarian stimulated cycles. METHODS GV oocytes (n = 234) were cultured in: (i) medium without the inhibitor (control); (ii) medium supplemented with 1 µM cilostamide and (iii) medium supplemented with 10 µM cilostamide. Oocytes in groups (ii) and (iii) were exposed to cilostamide for 24 h. The PDE3-I was subsequently removed by transfer of oocytes to fresh in vitro maturation (IVM) medium and the reversibility of GV arrest was assessed during IVM culture for maximum 48 h. RESULTS Cilostamide (1 and 10 µM) could maintain &gt;80% of the oocytes at the GV stage, without affecting subsequent maturation to metaphase II. Oocytes exposed to 1 µM cilostamide were more likely to have normal bipolar spindles with aligned chromosomes than control oocytes (P &lt; 0.05). When GV chromatin configurations before and after arrest were compared, a significantly higher proportion of oocytes had acquired a nucleolus completely surrounded by a rim of highly condensed chromatin (P &lt; 0.05). CONCLUSIONS Temporary nuclear arrest of human GV oocytes with PDE3-I proved to be beneficial for obtaining normal spindle and chromosome configurations after IVM. It resulted also in synchronization within the population of GV oocytes.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/dem007</identifier><identifier>PMID: 17303631</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Biological and medical sciences ; Cell Nucleus - drug effects ; Cell Nucleus - physiology ; Cells, Cultured ; Chromatin - drug effects ; Chromatin - ultrastructure ; Cytoplasm - physiology ; Embryonic Development - drug effects ; Female ; Gynecology. Andrology. Obstetrics ; Humans ; Medical sciences ; Meiosis - drug effects ; Oocytes - drug effects ; Oocytes - physiology ; Oocytes - ultrastructure ; Ovulation Induction - methods ; Phosphodiesterase Inhibitors - pharmacology ; Quinolones - pharmacology ; Spindle Apparatus - drug effects ; Spindle Apparatus - ultrastructure</subject><ispartof>Human reproduction (Oxford), 2007-05, Vol.22 (5), p.1239-1246</ispartof><rights>The Author 2007. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2007</rights><rights>2007 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) May 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-e77eb5ac2258b3e9803ae451d059bd8390f8e0a8cd591c38f382336ff7643e7d3</citedby><cites>FETCH-LOGICAL-c486t-e77eb5ac2258b3e9803ae451d059bd8390f8e0a8cd591c38f382336ff7643e7d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18764943$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17303631$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vanhoutte, Leen</creatorcontrib><creatorcontrib>De Sutter, Petra</creatorcontrib><creatorcontrib>Nogueira, Daniela</creatorcontrib><creatorcontrib>Gerris, Jan</creatorcontrib><creatorcontrib>Dhont, Marc</creatorcontrib><creatorcontrib>Van der Elst, Josiane</creatorcontrib><title>Nuclear and cytoplasmic maturation of in vitro matured human oocytes after temporary nuclear arrest by phosphodiesterase 3-inhibitor</title><title>Human reproduction (Oxford)</title><addtitle>Hum Reprod</addtitle><description>BACKGROUND The use of hormones for controlled ovarian stimulation results in follicular heterogeneity, with oocytes at diverse stages of nuclear and cytoplasmic development. This study evaluated the impact of temporary nuclear arrest by a specific phosphodiesterase 3-inhibitor (PDE3-I), cilostamide, on nuclear and cytoplasmic maturation of cumulus-free germinal vesicle (GV) human oocytes from controlled ovarian stimulated cycles. METHODS GV oocytes (n = 234) were cultured in: (i) medium without the inhibitor (control); (ii) medium supplemented with 1 µM cilostamide and (iii) medium supplemented with 10 µM cilostamide. Oocytes in groups (ii) and (iii) were exposed to cilostamide for 24 h. The PDE3-I was subsequently removed by transfer of oocytes to fresh in vitro maturation (IVM) medium and the reversibility of GV arrest was assessed during IVM culture for maximum 48 h. RESULTS Cilostamide (1 and 10 µM) could maintain &gt;80% of the oocytes at the GV stage, without affecting subsequent maturation to metaphase II. Oocytes exposed to 1 µM cilostamide were more likely to have normal bipolar spindles with aligned chromosomes than control oocytes (P &lt; 0.05). When GV chromatin configurations before and after arrest were compared, a significantly higher proportion of oocytes had acquired a nucleolus completely surrounded by a rim of highly condensed chromatin (P &lt; 0.05). CONCLUSIONS Temporary nuclear arrest of human GV oocytes with PDE3-I proved to be beneficial for obtaining normal spindle and chromosome configurations after IVM. It resulted also in synchronization within the population of GV oocytes.</description><subject>Biological and medical sciences</subject><subject>Cell Nucleus - drug effects</subject><subject>Cell Nucleus - physiology</subject><subject>Cells, Cultured</subject><subject>Chromatin - drug effects</subject><subject>Chromatin - ultrastructure</subject><subject>Cytoplasm - physiology</subject><subject>Embryonic Development - drug effects</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Meiosis - drug effects</subject><subject>Oocytes - drug effects</subject><subject>Oocytes - physiology</subject><subject>Oocytes - ultrastructure</subject><subject>Ovulation Induction - methods</subject><subject>Phosphodiesterase Inhibitors - pharmacology</subject><subject>Quinolones - pharmacology</subject><subject>Spindle Apparatus - drug effects</subject><subject>Spindle Apparatus - ultrastructure</subject><issn>0268-1161</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkcGL1TAQxoMo7tvVo1cJguKl7qTTpulRFl2FRS96Lmky4WVpm5qkwrv7hxvpkwUvHsIkmd98M8PH2AsB7wT0eH3c5kjrtaUZoHvEDqKRUNXYwmN2gFqqSggpLthlSvcA5arkU3YhOgSUKA7s15fNTKQj14vl5pTDOuk0e8Nnnbeosw8LD477hf_0OYb9mywvbXXJhFJCiWuXKfJM8xqijie-_BWNkVLm44mvx5DKsb68KepEHCu_HP3oc4jP2BOnp0TPz_GKff_44dvNp-ru6-3nm_d3lWmUzBV1HY2tNnXdqhGpV4CamlZYaPvRKuzBKQKtjG17YVA5VDWidK6TDVJn8Yq92XXXGH5sZZJh9snQNOmFwpaGDrBvQUIBX_0D3octLmW2oRaix7aBrkDVDpkYUorkhjX6uaw_CBj-eDPs3gy7N4V_eRbdxpnsA302owCvz4BORk8u6sX49MCpskffYOHe7lzY1v_0_A1jrqm9</recordid><startdate>20070501</startdate><enddate>20070501</enddate><creator>Vanhoutte, Leen</creator><creator>De Sutter, Petra</creator><creator>Nogueira, Daniela</creator><creator>Gerris, Jan</creator><creator>Dhont, Marc</creator><creator>Van der Elst, Josiane</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>IQODW</scope><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070501</creationdate><title>Nuclear and cytoplasmic maturation of in vitro matured human oocytes after temporary nuclear arrest by phosphodiesterase 3-inhibitor</title><author>Vanhoutte, Leen ; De Sutter, Petra ; Nogueira, Daniela ; Gerris, Jan ; Dhont, Marc ; Van der Elst, Josiane</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-e77eb5ac2258b3e9803ae451d059bd8390f8e0a8cd591c38f382336ff7643e7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Biological and medical sciences</topic><topic>Cell Nucleus - drug effects</topic><topic>Cell Nucleus - physiology</topic><topic>Cells, Cultured</topic><topic>Chromatin - drug effects</topic><topic>Chromatin - ultrastructure</topic><topic>Cytoplasm - physiology</topic><topic>Embryonic Development - drug effects</topic><topic>Female</topic><topic>Gynecology. 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Obstetrics</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Meiosis - drug effects</topic><topic>Oocytes - drug effects</topic><topic>Oocytes - physiology</topic><topic>Oocytes - ultrastructure</topic><topic>Ovulation Induction - methods</topic><topic>Phosphodiesterase Inhibitors - pharmacology</topic><topic>Quinolones - pharmacology</topic><topic>Spindle Apparatus - drug effects</topic><topic>Spindle Apparatus - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vanhoutte, Leen</creatorcontrib><creatorcontrib>De Sutter, Petra</creatorcontrib><creatorcontrib>Nogueira, Daniela</creatorcontrib><creatorcontrib>Gerris, Jan</creatorcontrib><creatorcontrib>Dhont, Marc</creatorcontrib><creatorcontrib>Van der Elst, Josiane</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vanhoutte, Leen</au><au>De Sutter, Petra</au><au>Nogueira, Daniela</au><au>Gerris, Jan</au><au>Dhont, Marc</au><au>Van der Elst, Josiane</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nuclear and cytoplasmic maturation of in vitro matured human oocytes after temporary nuclear arrest by phosphodiesterase 3-inhibitor</atitle><jtitle>Human reproduction (Oxford)</jtitle><addtitle>Hum Reprod</addtitle><date>2007-05-01</date><risdate>2007</risdate><volume>22</volume><issue>5</issue><spage>1239</spage><epage>1246</epage><pages>1239-1246</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>BACKGROUND The use of hormones for controlled ovarian stimulation results in follicular heterogeneity, with oocytes at diverse stages of nuclear and cytoplasmic development. This study evaluated the impact of temporary nuclear arrest by a specific phosphodiesterase 3-inhibitor (PDE3-I), cilostamide, on nuclear and cytoplasmic maturation of cumulus-free germinal vesicle (GV) human oocytes from controlled ovarian stimulated cycles. METHODS GV oocytes (n = 234) were cultured in: (i) medium without the inhibitor (control); (ii) medium supplemented with 1 µM cilostamide and (iii) medium supplemented with 10 µM cilostamide. Oocytes in groups (ii) and (iii) were exposed to cilostamide for 24 h. The PDE3-I was subsequently removed by transfer of oocytes to fresh in vitro maturation (IVM) medium and the reversibility of GV arrest was assessed during IVM culture for maximum 48 h. RESULTS Cilostamide (1 and 10 µM) could maintain &gt;80% of the oocytes at the GV stage, without affecting subsequent maturation to metaphase II. Oocytes exposed to 1 µM cilostamide were more likely to have normal bipolar spindles with aligned chromosomes than control oocytes (P &lt; 0.05). When GV chromatin configurations before and after arrest were compared, a significantly higher proportion of oocytes had acquired a nucleolus completely surrounded by a rim of highly condensed chromatin (P &lt; 0.05). CONCLUSIONS Temporary nuclear arrest of human GV oocytes with PDE3-I proved to be beneficial for obtaining normal spindle and chromosome configurations after IVM. It resulted also in synchronization within the population of GV oocytes.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>17303631</pmid><doi>10.1093/humrep/dem007</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source Oxford University Press:Jisc Collections:OUP Read and Publish 2024-2025 (2024 collection) (Reading list)
subjects Biological and medical sciences
Cell Nucleus - drug effects
Cell Nucleus - physiology
Cells, Cultured
Chromatin - drug effects
Chromatin - ultrastructure
Cytoplasm - physiology
Embryonic Development - drug effects
Female
Gynecology. Andrology. Obstetrics
Humans
Medical sciences
Meiosis - drug effects
Oocytes - drug effects
Oocytes - physiology
Oocytes - ultrastructure
Ovulation Induction - methods
Phosphodiesterase Inhibitors - pharmacology
Quinolones - pharmacology
Spindle Apparatus - drug effects
Spindle Apparatus - ultrastructure
title Nuclear and cytoplasmic maturation of in vitro matured human oocytes after temporary nuclear arrest by phosphodiesterase 3-inhibitor
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