PLCζ disruption with complete fertilization failure in normozoospermia

Purpose Intracytoplasmic sperm injection (ICSI) is widely used to achieve fertilization in the presence of severe male factor, resulting in high fertilization rates. Nevertheless, 1–3 % of couples experience complete fertilization failure after ICSI. When a male factor is identified, assisted oocyte...

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Veröffentlicht in:Journal of assisted reproduction and genetics 2015-06, Vol.32 (6), p.879-886
Hauptverfasser: Durban, Mercè, Barragán, Montserrat, Colodron, Marta, Ferrer-Buitrago, Minerva, De Sutter, Petra, Heindryckx, Björn, Vernaeve, Valérie, Vassena, Rita
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container_end_page 886
container_issue 6
container_start_page 879
container_title Journal of assisted reproduction and genetics
container_volume 32
creator Durban, Mercè
Barragán, Montserrat
Colodron, Marta
Ferrer-Buitrago, Minerva
De Sutter, Petra
Heindryckx, Björn
Vernaeve, Valérie
Vassena, Rita
description Purpose Intracytoplasmic sperm injection (ICSI) is widely used to achieve fertilization in the presence of severe male factor, resulting in high fertilization rates. Nevertheless, 1–3 % of couples experience complete fertilization failure after ICSI. When a male factor is identified, assisted oocyte activation (AOA) can help overcome fertilization failures. The objective of this study is to describe a case of repeated complete fertilization failures after ICSI with donor oocytes, and to investigate the molecular and functional aspects of phospholipase C zeta (PLCζ) protein in the patient semen. Methods The patient was a normozoospermic male who had previously fathered, through natural conception, four children by a different partner. Molecular and functional analysis of sperm-specific PLCζ in the patient and control samples by means of gene sequencing, immunocytochemistry, Western blot, mouse oocyte activation test (MOAT), and mouse oocyte calcium analysis (MOCA) were used. Results PLCζ expression levels and distribution were significantly disrupted, although MOAT and MOCA did not indicate a decrease in activation ability. Conclusions Normozoospermic males can have disrupted expression and distribution of PLCζ, and reduced activation ability after ICSI in human oocytes, despite their normal activation potential in functional testing using mouse oocytes. Discrepancy among molecular and functional data might exist, as mutations in the gene sequence may not be the only cause of alteration in PLCζ protein related to activation failures.
doi_str_mv 10.1007/s10815-015-0496-0
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Nevertheless, 1–3 % of couples experience complete fertilization failure after ICSI. When a male factor is identified, assisted oocyte activation (AOA) can help overcome fertilization failures. The objective of this study is to describe a case of repeated complete fertilization failures after ICSI with donor oocytes, and to investigate the molecular and functional aspects of phospholipase C zeta (PLCζ) protein in the patient semen. Methods The patient was a normozoospermic male who had previously fathered, through natural conception, four children by a different partner. Molecular and functional analysis of sperm-specific PLCζ in the patient and control samples by means of gene sequencing, immunocytochemistry, Western blot, mouse oocyte activation test (MOAT), and mouse oocyte calcium analysis (MOCA) were used. Results PLCζ expression levels and distribution were significantly disrupted, although MOAT and MOCA did not indicate a decrease in activation ability. Conclusions Normozoospermic males can have disrupted expression and distribution of PLCζ, and reduced activation ability after ICSI in human oocytes, despite their normal activation potential in functional testing using mouse oocytes. Discrepancy among molecular and functional data might exist, as mutations in the gene sequence may not be the only cause of alteration in PLCζ protein related to activation failures.</description><identifier>ISSN: 1058-0468</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/s10815-015-0496-0</identifier><identifier>PMID: 25986342</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Animals ; Calcium Ionophores - pharmacology ; Female ; Fertilization ; Gamete Biology ; Gynecology ; Human Genetics ; Humans ; Male ; Medicine ; Medicine &amp; Public Health ; Mice ; Middle Aged ; Oocytes - drug effects ; Phosphoinositide Phospholipase C - genetics ; Phosphoinositide Phospholipase C - metabolism ; Reproductive Medicine ; Semen Analysis ; Sperm Injections, Intracytoplasmic</subject><ispartof>Journal of assisted reproduction and genetics, 2015-06, Vol.32 (6), p.879-886</ispartof><rights>Springer Science+Business Media New York 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c545t-357ecc0b48eb396eeaa24583653b39cc6ccf4c5d5d1fe4687e51f597284872823</citedby><cites>FETCH-LOGICAL-c545t-357ecc0b48eb396eeaa24583653b39cc6ccf4c5d5d1fe4687e51f597284872823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491077/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491077/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,725,778,782,883,27911,27912,41475,42544,51306,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25986342$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Durban, Mercè</creatorcontrib><creatorcontrib>Barragán, Montserrat</creatorcontrib><creatorcontrib>Colodron, Marta</creatorcontrib><creatorcontrib>Ferrer-Buitrago, Minerva</creatorcontrib><creatorcontrib>De Sutter, Petra</creatorcontrib><creatorcontrib>Heindryckx, Björn</creatorcontrib><creatorcontrib>Vernaeve, Valérie</creatorcontrib><creatorcontrib>Vassena, Rita</creatorcontrib><title>PLCζ disruption with complete fertilization failure in normozoospermia</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><addtitle>J Assist Reprod Genet</addtitle><description>Purpose Intracytoplasmic sperm injection (ICSI) is widely used to achieve fertilization in the presence of severe male factor, resulting in high fertilization rates. Nevertheless, 1–3 % of couples experience complete fertilization failure after ICSI. When a male factor is identified, assisted oocyte activation (AOA) can help overcome fertilization failures. The objective of this study is to describe a case of repeated complete fertilization failures after ICSI with donor oocytes, and to investigate the molecular and functional aspects of phospholipase C zeta (PLCζ) protein in the patient semen. Methods The patient was a normozoospermic male who had previously fathered, through natural conception, four children by a different partner. Molecular and functional analysis of sperm-specific PLCζ in the patient and control samples by means of gene sequencing, immunocytochemistry, Western blot, mouse oocyte activation test (MOAT), and mouse oocyte calcium analysis (MOCA) were used. Results PLCζ expression levels and distribution were significantly disrupted, although MOAT and MOCA did not indicate a decrease in activation ability. Conclusions Normozoospermic males can have disrupted expression and distribution of PLCζ, and reduced activation ability after ICSI in human oocytes, despite their normal activation potential in functional testing using mouse oocytes. Discrepancy among molecular and functional data might exist, as mutations in the gene sequence may not be the only cause of alteration in PLCζ protein related to activation failures.</description><subject>Animals</subject><subject>Calcium Ionophores - pharmacology</subject><subject>Female</subject><subject>Fertilization</subject><subject>Gamete Biology</subject><subject>Gynecology</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Mice</subject><subject>Middle Aged</subject><subject>Oocytes - drug effects</subject><subject>Phosphoinositide Phospholipase C - genetics</subject><subject>Phosphoinositide Phospholipase C - metabolism</subject><subject>Reproductive Medicine</subject><subject>Semen Analysis</subject><subject>Sperm Injections, Intracytoplasmic</subject><issn>1058-0468</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUctOHDEQtKKg8Eg-gAuaYy5D2mN7bF-Q0IpHpJXCAc6W19uzGM2MB3smUfgwPoNvwstuEFzIodtuVXWp7CLkkMIxBZA_EgVFRQnr4rou4RPZo0KyUjIGn_MdhMpIrXbJfkp3AKBVxb6Q3UpoVTNe7ZGLq_ns6bFY-hSnYfShL_748bZwoRtaHLFoMI6-9Q_2BWusb6eIhe-LPsQuPISQBoydt1_JTmPbhN-25wG5OT-7nl2W818XP2en89IJLsaSCYnOwYIrXDBdI1pbcaFYLVienauda7gTS7GkDWbjEgVthJaV4iq3ih2Qk43uMC06XDrsx2hbM0Tf2fjXBOvNe6T3t2YVfhvONQUps8D3rUAM9xOm0XQ-OWxb22OYkqESNNUgsqn_UmvNJKPyhUo3VBdDShGbV0cUzDors8nKwLpyVgbyztHbp7xu_AsnE6oNIWWoX2E0d2GKff7eD1SfAXggoUc</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Durban, Mercè</creator><creator>Barragán, Montserrat</creator><creator>Colodron, Marta</creator><creator>Ferrer-Buitrago, Minerva</creator><creator>De Sutter, Petra</creator><creator>Heindryckx, Björn</creator><creator>Vernaeve, Valérie</creator><creator>Vassena, Rita</creator><general>Springer US</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>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20150601</creationdate><title>PLCζ disruption with complete fertilization failure in normozoospermia</title><author>Durban, Mercè ; Barragán, Montserrat ; Colodron, Marta ; Ferrer-Buitrago, Minerva ; De Sutter, Petra ; Heindryckx, Björn ; Vernaeve, Valérie ; Vassena, Rita</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c545t-357ecc0b48eb396eeaa24583653b39cc6ccf4c5d5d1fe4687e51f597284872823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Calcium Ionophores - pharmacology</topic><topic>Female</topic><topic>Fertilization</topic><topic>Gamete Biology</topic><topic>Gynecology</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Mice</topic><topic>Middle Aged</topic><topic>Oocytes - drug effects</topic><topic>Phosphoinositide Phospholipase C - genetics</topic><topic>Phosphoinositide Phospholipase C - metabolism</topic><topic>Reproductive Medicine</topic><topic>Semen Analysis</topic><topic>Sperm Injections, Intracytoplasmic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Durban, Mercè</creatorcontrib><creatorcontrib>Barragán, Montserrat</creatorcontrib><creatorcontrib>Colodron, Marta</creatorcontrib><creatorcontrib>Ferrer-Buitrago, Minerva</creatorcontrib><creatorcontrib>De Sutter, Petra</creatorcontrib><creatorcontrib>Heindryckx, Björn</creatorcontrib><creatorcontrib>Vernaeve, Valérie</creatorcontrib><creatorcontrib>Vassena, Rita</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><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of assisted reproduction and genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Durban, Mercè</au><au>Barragán, Montserrat</au><au>Colodron, Marta</au><au>Ferrer-Buitrago, Minerva</au><au>De Sutter, Petra</au><au>Heindryckx, Björn</au><au>Vernaeve, Valérie</au><au>Vassena, Rita</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PLCζ disruption with complete fertilization failure in normozoospermia</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><stitle>J Assist Reprod Genet</stitle><addtitle>J Assist Reprod Genet</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>32</volume><issue>6</issue><spage>879</spage><epage>886</epage><pages>879-886</pages><issn>1058-0468</issn><eissn>1573-7330</eissn><abstract>Purpose Intracytoplasmic sperm injection (ICSI) is widely used to achieve fertilization in the presence of severe male factor, resulting in high fertilization rates. Nevertheless, 1–3 % of couples experience complete fertilization failure after ICSI. When a male factor is identified, assisted oocyte activation (AOA) can help overcome fertilization failures. The objective of this study is to describe a case of repeated complete fertilization failures after ICSI with donor oocytes, and to investigate the molecular and functional aspects of phospholipase C zeta (PLCζ) protein in the patient semen. Methods The patient was a normozoospermic male who had previously fathered, through natural conception, four children by a different partner. Molecular and functional analysis of sperm-specific PLCζ in the patient and control samples by means of gene sequencing, immunocytochemistry, Western blot, mouse oocyte activation test (MOAT), and mouse oocyte calcium analysis (MOCA) were used. Results PLCζ expression levels and distribution were significantly disrupted, although MOAT and MOCA did not indicate a decrease in activation ability. Conclusions Normozoospermic males can have disrupted expression and distribution of PLCζ, and reduced activation ability after ICSI in human oocytes, despite their normal activation potential in functional testing using mouse oocytes. Discrepancy among molecular and functional data might exist, as mutations in the gene sequence may not be the only cause of alteration in PLCζ protein related to activation failures.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>25986342</pmid><doi>10.1007/s10815-015-0496-0</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature - Complete Springer Journals; PubMed Central
subjects Animals
Calcium Ionophores - pharmacology
Female
Fertilization
Gamete Biology
Gynecology
Human Genetics
Humans
Male
Medicine
Medicine & Public Health
Mice
Middle Aged
Oocytes - drug effects
Phosphoinositide Phospholipase C - genetics
Phosphoinositide Phospholipase C - metabolism
Reproductive Medicine
Semen Analysis
Sperm Injections, Intracytoplasmic
title PLCζ disruption with complete fertilization failure in normozoospermia
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