The effect of lysophosphatidic acid during in vitro maturation of bovine cumulus-oocyte complexes: cumulus expansion, glucose metabolism and expression of genes involved in the ovulatory cascade, oocyte and blastocyst competence
In the cow, lysophosphatidic acid (LPA) acts as an auto-/paracrine factor, through its receptors LPAR1-4, on oocytes and cumulus cells during in vitro maturation (IVM). The aim of the present work was to determine the effect of LPA during IVM of bovine oocytes on: 1) oocyte maturation; 2) apoptosis...
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description | In the cow, lysophosphatidic acid (LPA) acts as an auto-/paracrine factor, through its receptors LPAR1-4, on oocytes and cumulus cells during in vitro maturation (IVM). The aim of the present work was to determine the effect of LPA during IVM of bovine oocytes on: 1) oocyte maturation; 2) apoptosis of COCs; 3) expression of genes involved in developmental competence and apoptosis in bovine oocytes and subsequent blastocysts; 4) cumulus expansion and expression of genes involved in the ovulatory cascade in cumulus cells; 5) glucose metabolism and expression of genes involved in glucose utilization in cumulus cells; 6) cleavage and blastocyst rates on Day 2 and Day 7 of in vitro culture, respectively.
Cumulus-oocyte complexes (COCs) were matured in vitro in the presence or absence of LPA (10(-5) M) for 24 h. Following maturation, we determined: oocyte maturation stage, cumulus expansion, COCs apoptosis and glucose and lactate levels in the maturation medium. Moreover, COCs were either used for gene expression analysis or fertilized in vitro. The embryos were cultured until Day 7 to assess cleavage and blastocyst rates. Oocytes, cumulus cells and blastocysts were used for gene expression analysis.
Supplementation of the maturation medium with LPA enhanced oocyte maturation rates and stimulated the expression of developmental competence-related factors (OCT4, SOX2, IGF2R) in oocytes and subsequent blastocysts. Moreover, LPA reduced the occurrence of apoptosis in COCs and promoted an antiapoptotic balance in the transcription of genes involved in apoptosis (BAX and BCL2) either in oocytes or blastocysts. LPA increased glucose uptake by COCs via augmentation of GLUT1 expression in cumulus cells as well as stimulating lactate production via the enhancement of PFKP expression in cumulus cells. LPA did not affect cumulus expansion as visually assessed, however, it stimulated upstream genes of cumulus expansion cascade, AREG and EREG.
Supplementation of the maturation medium with LPA improves oocyte maturation rates, decreases extent of apoptosis in COCs and sustains the expression of developmental competence related factors during oocyte maturation and subsequently affects gene expression profile at the blastocyst stage. We also demonstrate that LPA directs glucose metabolism toward the glycolytic pathway during IVM. |
doi_str_mv | 10.1186/s12958-015-0044-x |
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Cumulus-oocyte complexes (COCs) were matured in vitro in the presence or absence of LPA (10(-5) M) for 24 h. Following maturation, we determined: oocyte maturation stage, cumulus expansion, COCs apoptosis and glucose and lactate levels in the maturation medium. Moreover, COCs were either used for gene expression analysis or fertilized in vitro. The embryos were cultured until Day 7 to assess cleavage and blastocyst rates. Oocytes, cumulus cells and blastocysts were used for gene expression analysis.
Supplementation of the maturation medium with LPA enhanced oocyte maturation rates and stimulated the expression of developmental competence-related factors (OCT4, SOX2, IGF2R) in oocytes and subsequent blastocysts. Moreover, LPA reduced the occurrence of apoptosis in COCs and promoted an antiapoptotic balance in the transcription of genes involved in apoptosis (BAX and BCL2) either in oocytes or blastocysts. LPA increased glucose uptake by COCs via augmentation of GLUT1 expression in cumulus cells as well as stimulating lactate production via the enhancement of PFKP expression in cumulus cells. LPA did not affect cumulus expansion as visually assessed, however, it stimulated upstream genes of cumulus expansion cascade, AREG and EREG.
Supplementation of the maturation medium with LPA improves oocyte maturation rates, decreases extent of apoptosis in COCs and sustains the expression of developmental competence related factors during oocyte maturation and subsequently affects gene expression profile at the blastocyst stage. We also demonstrate that LPA directs glucose metabolism toward the glycolytic pathway during IVM.</description><identifier>ISSN: 1477-7827</identifier><identifier>EISSN: 1477-7827</identifier><identifier>DOI: 10.1186/s12958-015-0044-x</identifier><identifier>PMID: 25981539</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Animals ; Apoptosis ; Apoptosis - drug effects ; Blastocyst - drug effects ; Cattle ; Cumulus Cells - drug effects ; Dextrose ; Embryo Culture Techniques ; Female ; Gene Expression Regulation, Developmental ; Genes ; Genetic aspects ; Genetic research ; Genetic transcription ; Glucose ; Glucose - metabolism ; In Vitro Oocyte Maturation Techniques - methods ; Lactates ; Lysophospholipids - pharmacology ; Oocytes - drug effects ; Oocytes - growth & development ; Ovulation - genetics ; Physiological aspects</subject><ispartof>Reproductive biology and endocrinology, 2015-05, Vol.13 (1), p.44-44, Article 44</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Boruszewska et al.; licensee BioMed Central. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c602t-9836d0e21344ab9537090e2ecd42db16940feb8032818eb2a3777e9d6e7c0f4b3</citedby><cites>FETCH-LOGICAL-c602t-9836d0e21344ab9537090e2ecd42db16940feb8032818eb2a3777e9d6e7c0f4b3</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/PMC4438640/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438640/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25981539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boruszewska, Dorota</creatorcontrib><creatorcontrib>Sinderewicz, Emilia</creatorcontrib><creatorcontrib>Kowalczyk-Zieba, Ilona</creatorcontrib><creatorcontrib>Grycmacher, Katarzyna</creatorcontrib><creatorcontrib>Woclawek-Potocka, Izabela</creatorcontrib><title>The effect of lysophosphatidic acid during in vitro maturation of bovine cumulus-oocyte complexes: cumulus expansion, glucose metabolism and expression of genes involved in the ovulatory cascade, oocyte and blastocyst competence</title><title>Reproductive biology and endocrinology</title><addtitle>Reprod Biol Endocrinol</addtitle><description>In the cow, lysophosphatidic acid (LPA) acts as an auto-/paracrine factor, through its receptors LPAR1-4, on oocytes and cumulus cells during in vitro maturation (IVM). The aim of the present work was to determine the effect of LPA during IVM of bovine oocytes on: 1) oocyte maturation; 2) apoptosis of COCs; 3) expression of genes involved in developmental competence and apoptosis in bovine oocytes and subsequent blastocysts; 4) cumulus expansion and expression of genes involved in the ovulatory cascade in cumulus cells; 5) glucose metabolism and expression of genes involved in glucose utilization in cumulus cells; 6) cleavage and blastocyst rates on Day 2 and Day 7 of in vitro culture, respectively.
Cumulus-oocyte complexes (COCs) were matured in vitro in the presence or absence of LPA (10(-5) M) for 24 h. Following maturation, we determined: oocyte maturation stage, cumulus expansion, COCs apoptosis and glucose and lactate levels in the maturation medium. Moreover, COCs were either used for gene expression analysis or fertilized in vitro. The embryos were cultured until Day 7 to assess cleavage and blastocyst rates. Oocytes, cumulus cells and blastocysts were used for gene expression analysis.
Supplementation of the maturation medium with LPA enhanced oocyte maturation rates and stimulated the expression of developmental competence-related factors (OCT4, SOX2, IGF2R) in oocytes and subsequent blastocysts. Moreover, LPA reduced the occurrence of apoptosis in COCs and promoted an antiapoptotic balance in the transcription of genes involved in apoptosis (BAX and BCL2) either in oocytes or blastocysts. LPA increased glucose uptake by COCs via augmentation of GLUT1 expression in cumulus cells as well as stimulating lactate production via the enhancement of PFKP expression in cumulus cells. LPA did not affect cumulus expansion as visually assessed, however, it stimulated upstream genes of cumulus expansion cascade, AREG and EREG.
Supplementation of the maturation medium with LPA improves oocyte maturation rates, decreases extent of apoptosis in COCs and sustains the expression of developmental competence related factors during oocyte maturation and subsequently affects gene expression profile at the blastocyst stage. We also demonstrate that LPA directs glucose metabolism toward the glycolytic pathway during IVM.</description><subject>Analysis</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Blastocyst - drug effects</subject><subject>Cattle</subject><subject>Cumulus Cells - drug effects</subject><subject>Dextrose</subject><subject>Embryo Culture Techniques</subject><subject>Female</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic research</subject><subject>Genetic transcription</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>In Vitro Oocyte Maturation Techniques - methods</subject><subject>Lactates</subject><subject>Lysophospholipids - pharmacology</subject><subject>Oocytes - drug effects</subject><subject>Oocytes - growth & development</subject><subject>Ovulation - genetics</subject><subject>Physiological aspects</subject><issn>1477-7827</issn><issn>1477-7827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptUs2O1SAUbozG-dEHcGNI3LiYjkBpS11MMpk4ajKJm3FNKJzei6FQgTb3vq8PIvXemcwkruBwvp8DfEXxjuBLQnjzKRLa1bzEpC4xZqzcvShOCWvbsuW0fflkf1KcxfgLY4oxb14XJ7TuOKmr7rT4c78FBMMAKiE_ILuPftr6OG1lMtooJJXRSM_BuA0yDi0mBY9GmeaQAd6tnN4vxgFS8zjbOZbeq33KpR8nCzuInx86CHaTdDGzLtDGzspHQCMk2Xtr4oik0ysiQIxH4Q04iNl18XYBvdqnPKxfZiuTD3ukZFRSwwU6Wq4KvZUx5TKmfxNAAqfgTfFqkDbC2-N6Xvy8_XJ_8628-_H1-831XakaTFPZ8arRGCipGJN9V1ct7nIJSjOqe9J0DA_Qc1xRTjj0VFZt20KnG2gVHlhfnRdXB91p7kfQClwK0oopmFGGvfDSiOcdZ7Zi4xfBWMUbhrPAx6NA8L9niEmMJiqwVjrwcxSk4ZTR_KssQz8coBtpQRg3-KyoVri4rhmpccOqOqMu_4OS67ONRnkHg8nnzwjkQFDBxxhgeJyeYLGGThxCJ3LoxBo6scuc90-v_ch4SFn1FyCr2jQ</recordid><startdate>20150516</startdate><enddate>20150516</enddate><creator>Boruszewska, Dorota</creator><creator>Sinderewicz, Emilia</creator><creator>Kowalczyk-Zieba, Ilona</creator><creator>Grycmacher, Katarzyna</creator><creator>Woclawek-Potocka, Izabela</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>5PM</scope></search><sort><creationdate>20150516</creationdate><title>The effect of lysophosphatidic acid during in vitro maturation of bovine cumulus-oocyte complexes: cumulus expansion, glucose metabolism and expression of genes involved in the ovulatory cascade, oocyte and blastocyst competence</title><author>Boruszewska, Dorota ; Sinderewicz, Emilia ; Kowalczyk-Zieba, Ilona ; Grycmacher, Katarzyna ; Woclawek-Potocka, Izabela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c602t-9836d0e21344ab9537090e2ecd42db16940feb8032818eb2a3777e9d6e7c0f4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Blastocyst - drug effects</topic><topic>Cattle</topic><topic>Cumulus Cells - drug effects</topic><topic>Dextrose</topic><topic>Embryo Culture Techniques</topic><topic>Female</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic research</topic><topic>Genetic transcription</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>In Vitro Oocyte Maturation Techniques - methods</topic><topic>Lactates</topic><topic>Lysophospholipids - pharmacology</topic><topic>Oocytes - drug effects</topic><topic>Oocytes - growth & development</topic><topic>Ovulation - genetics</topic><topic>Physiological aspects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boruszewska, Dorota</creatorcontrib><creatorcontrib>Sinderewicz, Emilia</creatorcontrib><creatorcontrib>Kowalczyk-Zieba, Ilona</creatorcontrib><creatorcontrib>Grycmacher, Katarzyna</creatorcontrib><creatorcontrib>Woclawek-Potocka, Izabela</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>PubMed Central (Full Participant titles)</collection><jtitle>Reproductive biology and endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boruszewska, Dorota</au><au>Sinderewicz, Emilia</au><au>Kowalczyk-Zieba, Ilona</au><au>Grycmacher, Katarzyna</au><au>Woclawek-Potocka, Izabela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of lysophosphatidic acid during in vitro maturation of bovine cumulus-oocyte complexes: cumulus expansion, glucose metabolism and expression of genes involved in the ovulatory cascade, oocyte and blastocyst competence</atitle><jtitle>Reproductive biology and endocrinology</jtitle><addtitle>Reprod Biol Endocrinol</addtitle><date>2015-05-16</date><risdate>2015</risdate><volume>13</volume><issue>1</issue><spage>44</spage><epage>44</epage><pages>44-44</pages><artnum>44</artnum><issn>1477-7827</issn><eissn>1477-7827</eissn><abstract>In the cow, lysophosphatidic acid (LPA) acts as an auto-/paracrine factor, through its receptors LPAR1-4, on oocytes and cumulus cells during in vitro maturation (IVM). The aim of the present work was to determine the effect of LPA during IVM of bovine oocytes on: 1) oocyte maturation; 2) apoptosis of COCs; 3) expression of genes involved in developmental competence and apoptosis in bovine oocytes and subsequent blastocysts; 4) cumulus expansion and expression of genes involved in the ovulatory cascade in cumulus cells; 5) glucose metabolism and expression of genes involved in glucose utilization in cumulus cells; 6) cleavage and blastocyst rates on Day 2 and Day 7 of in vitro culture, respectively.
Cumulus-oocyte complexes (COCs) were matured in vitro in the presence or absence of LPA (10(-5) M) for 24 h. Following maturation, we determined: oocyte maturation stage, cumulus expansion, COCs apoptosis and glucose and lactate levels in the maturation medium. Moreover, COCs were either used for gene expression analysis or fertilized in vitro. The embryos were cultured until Day 7 to assess cleavage and blastocyst rates. Oocytes, cumulus cells and blastocysts were used for gene expression analysis.
Supplementation of the maturation medium with LPA enhanced oocyte maturation rates and stimulated the expression of developmental competence-related factors (OCT4, SOX2, IGF2R) in oocytes and subsequent blastocysts. Moreover, LPA reduced the occurrence of apoptosis in COCs and promoted an antiapoptotic balance in the transcription of genes involved in apoptosis (BAX and BCL2) either in oocytes or blastocysts. LPA increased glucose uptake by COCs via augmentation of GLUT1 expression in cumulus cells as well as stimulating lactate production via the enhancement of PFKP expression in cumulus cells. LPA did not affect cumulus expansion as visually assessed, however, it stimulated upstream genes of cumulus expansion cascade, AREG and EREG.
Supplementation of the maturation medium with LPA improves oocyte maturation rates, decreases extent of apoptosis in COCs and sustains the expression of developmental competence related factors during oocyte maturation and subsequently affects gene expression profile at the blastocyst stage. We also demonstrate that LPA directs glucose metabolism toward the glycolytic pathway during IVM.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>25981539</pmid><doi>10.1186/s12958-015-0044-x</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Apoptosis Apoptosis - drug effects Blastocyst - drug effects Cattle Cumulus Cells - drug effects Dextrose Embryo Culture Techniques Female Gene Expression Regulation, Developmental Genes Genetic aspects Genetic research Genetic transcription Glucose Glucose - metabolism In Vitro Oocyte Maturation Techniques - methods Lactates Lysophospholipids - pharmacology Oocytes - drug effects Oocytes - growth & development Ovulation - genetics Physiological aspects |
title | The effect of lysophosphatidic acid during in vitro maturation of bovine cumulus-oocyte complexes: cumulus expansion, glucose metabolism and expression of genes involved in the ovulatory cascade, oocyte and blastocyst competence |
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