Delay on the in vitro kinetic development of prepubertal ovine embryos
In the present study we characterize the developmental potential of prepubertal and adult ovine oocytes, analyzing the developmental speed to two-cell and blastocyst stages and its relationship with hatching from the zona pellucida, development after vitrification and the number and allocation of in...
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Veröffentlicht in: | Animal reproduction science 2006-05, Vol.92 (3), p.373-383 |
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creator | Leoni, G.G. Succu, S. Berlinguer, F. Rosati, I. Bebbere, D. Bogliolo, L. Ledda, S. Naitana, S. |
description | In the present study we characterize the developmental potential of prepubertal and adult ovine oocytes, analyzing the developmental speed to two-cell and blastocyst stages and its relationship with hatching from the zona pellucida, development after vitrification and the number and allocation of inner mass and trophoblastic cells. Prepubertal and adult ovine oocytes were matured and fertilized in vitro and first cleavage rates at 22, 26 and 32
h were recorded. Cleaved oocytes were cultured and blastocyst production was assessed at 6–9 days post-fertilization (dpf). Blastocysts from the two sources obtained on different days were divided into two groups: the first was vitrified, warmed and cultured in vitro to evaluate re-expansion of the blastocoelic cavity; blastocysts of the second were cultured separately to allow for hatching and count of trophoblastic and inner mass cells of hatched blastocysts by differential staining. We observed a significantly lower rate (
P
<
0.01) of cleaved prepubertal oocytes at 22 and 26
h after fertilization while it was higher (
P
<
0.01) at 32
h than in the adult ones. Adult blastocyst production was significantly lower (
P
<
0.01) in prepubertal than in adult groups and began on the seventh dpf, later (
P
<
0.01) than in the adult group, where they appeared on the sixth dpf. Prepubertal blastocysts hatched at a lower rate than the adult ones (
P
<
0.01) and in both experimental groups faster blastocysts showed a higher (
P
<
0.01) hatching rate. Similarly, prepubertal derived blastocysts showed lower viability after vitrification (
P
<
0.01) compared to the adult counterparts, and in particular slower embryos had reduced viability after vitrification compared to the fastest (
P
<
0.01). Cell number was not different between blastocysts of both groups obtained at 6 and 7
dpf, which were higher (
P
<
0.01) than those obtained at 8 and 9
dpf. The ICM/trophoblast cell ratio was similar in 6- and 7-day obtained blastocyst and increased (
P
<
0.01) in those obtained 1 or 2 days later. These findings show that differences in kinetic development between prepubertal and adult derived embryos reflect differences in developmental capacity of the oocytes from which they derive and could be indicative of embryo quality. |
doi_str_mv | 10.1016/j.anireprosci.2005.05.027 |
format | Article |
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h were recorded. Cleaved oocytes were cultured and blastocyst production was assessed at 6–9 days post-fertilization (dpf). Blastocysts from the two sources obtained on different days were divided into two groups: the first was vitrified, warmed and cultured in vitro to evaluate re-expansion of the blastocoelic cavity; blastocysts of the second were cultured separately to allow for hatching and count of trophoblastic and inner mass cells of hatched blastocysts by differential staining. We observed a significantly lower rate (
P
<
0.01) of cleaved prepubertal oocytes at 22 and 26
h after fertilization while it was higher (
P
<
0.01) at 32
h than in the adult ones. Adult blastocyst production was significantly lower (
P
<
0.01) in prepubertal than in adult groups and began on the seventh dpf, later (
P
<
0.01) than in the adult group, where they appeared on the sixth dpf. Prepubertal blastocysts hatched at a lower rate than the adult ones (
P
<
0.01) and in both experimental groups faster blastocysts showed a higher (
P
<
0.01) hatching rate. Similarly, prepubertal derived blastocysts showed lower viability after vitrification (
P
<
0.01) compared to the adult counterparts, and in particular slower embryos had reduced viability after vitrification compared to the fastest (
P
<
0.01). Cell number was not different between blastocysts of both groups obtained at 6 and 7
dpf, which were higher (
P
<
0.01) than those obtained at 8 and 9
dpf. The ICM/trophoblast cell ratio was similar in 6- and 7-day obtained blastocyst and increased (
P
<
0.01) in those obtained 1 or 2 days later. These findings show that differences in kinetic development between prepubertal and adult derived embryos reflect differences in developmental capacity of the oocytes from which they derive and could be indicative of embryo quality.]]></description><identifier>ISSN: 0378-4320</identifier><identifier>EISSN: 1873-2232</identifier><identifier>DOI: 10.1016/j.anireprosci.2005.05.027</identifier><identifier>PMID: 16054784</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; blastocyst ; Blastocyst - physiology ; cell culture ; Cell Division ; Cleavage Stage, Ovum - physiology ; embryo (animal) ; Embryo Culture Techniques - veterinary ; embryogenesis ; Embryonic Development - physiology ; ewes ; Female ; Fertilization in Vitro - veterinary ; Kinetics ; Kinetics cleavage ; Male ; Oocyte ; oocytes ; Ovine ; Prepubertal ; Sexual Maturation - physiology ; Sheep - embryology ; Time Factors ; tissue culture ; trophoblast ; viability ; vitrification ; vitrified oocysts ; zona pellucida</subject><ispartof>Animal reproduction science, 2006-05, Vol.92 (3), p.373-383</ispartof><rights>2005 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c496t-6ba8e1e4ab45dabbf88896f36cdc36f2c93e2b142c24f025d450bf8fca94fd533</citedby><cites>FETCH-LOGICAL-c496t-6ba8e1e4ab45dabbf88896f36cdc36f2c93e2b142c24f025d450bf8fca94fd533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S037843200500165X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16054784$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leoni, G.G.</creatorcontrib><creatorcontrib>Succu, S.</creatorcontrib><creatorcontrib>Berlinguer, F.</creatorcontrib><creatorcontrib>Rosati, I.</creatorcontrib><creatorcontrib>Bebbere, D.</creatorcontrib><creatorcontrib>Bogliolo, L.</creatorcontrib><creatorcontrib>Ledda, S.</creatorcontrib><creatorcontrib>Naitana, S.</creatorcontrib><title>Delay on the in vitro kinetic development of prepubertal ovine embryos</title><title>Animal reproduction science</title><addtitle>Anim Reprod Sci</addtitle><description><![CDATA[In the present study we characterize the developmental potential of prepubertal and adult ovine oocytes, analyzing the developmental speed to two-cell and blastocyst stages and its relationship with hatching from the zona pellucida, development after vitrification and the number and allocation of inner mass and trophoblastic cells. Prepubertal and adult ovine oocytes were matured and fertilized in vitro and first cleavage rates at 22, 26 and 32
h were recorded. Cleaved oocytes were cultured and blastocyst production was assessed at 6–9 days post-fertilization (dpf). Blastocysts from the two sources obtained on different days were divided into two groups: the first was vitrified, warmed and cultured in vitro to evaluate re-expansion of the blastocoelic cavity; blastocysts of the second were cultured separately to allow for hatching and count of trophoblastic and inner mass cells of hatched blastocysts by differential staining. We observed a significantly lower rate (
P
<
0.01) of cleaved prepubertal oocytes at 22 and 26
h after fertilization while it was higher (
P
<
0.01) at 32
h than in the adult ones. Adult blastocyst production was significantly lower (
P
<
0.01) in prepubertal than in adult groups and began on the seventh dpf, later (
P
<
0.01) than in the adult group, where they appeared on the sixth dpf. Prepubertal blastocysts hatched at a lower rate than the adult ones (
P
<
0.01) and in both experimental groups faster blastocysts showed a higher (
P
<
0.01) hatching rate. Similarly, prepubertal derived blastocysts showed lower viability after vitrification (
P
<
0.01) compared to the adult counterparts, and in particular slower embryos had reduced viability after vitrification compared to the fastest (
P
<
0.01). Cell number was not different between blastocysts of both groups obtained at 6 and 7
dpf, which were higher (
P
<
0.01) than those obtained at 8 and 9
dpf. The ICM/trophoblast cell ratio was similar in 6- and 7-day obtained blastocyst and increased (
P
<
0.01) in those obtained 1 or 2 days later. These findings show that differences in kinetic development between prepubertal and adult derived embryos reflect differences in developmental capacity of the oocytes from which they derive and could be indicative of embryo quality.]]></description><subject>Animals</subject><subject>blastocyst</subject><subject>Blastocyst - physiology</subject><subject>cell culture</subject><subject>Cell Division</subject><subject>Cleavage Stage, Ovum - physiology</subject><subject>embryo (animal)</subject><subject>Embryo Culture Techniques - veterinary</subject><subject>embryogenesis</subject><subject>Embryonic Development - physiology</subject><subject>ewes</subject><subject>Female</subject><subject>Fertilization in Vitro - veterinary</subject><subject>Kinetics</subject><subject>Kinetics cleavage</subject><subject>Male</subject><subject>Oocyte</subject><subject>oocytes</subject><subject>Ovine</subject><subject>Prepubertal</subject><subject>Sexual Maturation - physiology</subject><subject>Sheep - embryology</subject><subject>Time Factors</subject><subject>tissue culture</subject><subject>trophoblast</subject><subject>viability</subject><subject>vitrification</subject><subject>vitrified oocysts</subject><subject>zona pellucida</subject><issn>0378-4320</issn><issn>1873-2232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtO4zAUQK0RaCjM_AKYzexS_IqdLFGhAxISC4a15TjX4JLExU4r9e_HUSvBDqQreXOuj30QuqRkTgmVV6u5GXyEdQzJ-jkjpJxPw9QPNKOV4gVjnB2hGeGqKgRn5ASdprQihCgp65_ohEpSClWJGVreQGd2OAx4fAXsB7z1Ywz4zQ8weotb2EIX1j0MIw4Or7N000AcTYfDNjMY-ibuQvqFjp3pEvw-nGfoeXn7b3FXPDz-vV9cPxRW1HIsZGMqoCBMI8rWNI2rqqqWjkvbWi4dszUH1lDBLBOOsLIVJcmQs6YWri05P0N_9vfmv79vII2698lC15kBwiZpqSpWSym-BGktBFOyzGC9B22umSI4vY6-N3GnKdFTbb3Sn2rrqbaehqm8e36QbJoe2o_NQ94MXOwBZ4I2L9En_fzECOWEUqpKPukXewJyta2HqLMEBgttVtpRt8F_4yH_AV_roRo</recordid><startdate>20060501</startdate><enddate>20060501</enddate><creator>Leoni, G.G.</creator><creator>Succu, S.</creator><creator>Berlinguer, F.</creator><creator>Rosati, I.</creator><creator>Bebbere, D.</creator><creator>Bogliolo, L.</creator><creator>Ledda, S.</creator><creator>Naitana, S.</creator><general>Elsevier B.V</general><scope>FBQ</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20060501</creationdate><title>Delay on the in vitro kinetic development of prepubertal ovine embryos</title><author>Leoni, G.G. ; Succu, S. ; Berlinguer, F. ; Rosati, I. ; Bebbere, D. ; Bogliolo, L. ; Ledda, S. ; Naitana, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-6ba8e1e4ab45dabbf88896f36cdc36f2c93e2b142c24f025d450bf8fca94fd533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>blastocyst</topic><topic>Blastocyst - physiology</topic><topic>cell culture</topic><topic>Cell Division</topic><topic>Cleavage Stage, Ovum - physiology</topic><topic>embryo (animal)</topic><topic>Embryo Culture Techniques - veterinary</topic><topic>embryogenesis</topic><topic>Embryonic Development - physiology</topic><topic>ewes</topic><topic>Female</topic><topic>Fertilization in Vitro - veterinary</topic><topic>Kinetics</topic><topic>Kinetics cleavage</topic><topic>Male</topic><topic>Oocyte</topic><topic>oocytes</topic><topic>Ovine</topic><topic>Prepubertal</topic><topic>Sexual Maturation - physiology</topic><topic>Sheep - embryology</topic><topic>Time Factors</topic><topic>tissue culture</topic><topic>trophoblast</topic><topic>viability</topic><topic>vitrification</topic><topic>vitrified oocysts</topic><topic>zona pellucida</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leoni, G.G.</creatorcontrib><creatorcontrib>Succu, S.</creatorcontrib><creatorcontrib>Berlinguer, F.</creatorcontrib><creatorcontrib>Rosati, I.</creatorcontrib><creatorcontrib>Bebbere, D.</creatorcontrib><creatorcontrib>Bogliolo, L.</creatorcontrib><creatorcontrib>Ledda, S.</creatorcontrib><creatorcontrib>Naitana, S.</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Animal reproduction science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leoni, G.G.</au><au>Succu, S.</au><au>Berlinguer, F.</au><au>Rosati, I.</au><au>Bebbere, D.</au><au>Bogliolo, L.</au><au>Ledda, S.</au><au>Naitana, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Delay on the in vitro kinetic development of prepubertal ovine embryos</atitle><jtitle>Animal reproduction science</jtitle><addtitle>Anim Reprod Sci</addtitle><date>2006-05-01</date><risdate>2006</risdate><volume>92</volume><issue>3</issue><spage>373</spage><epage>383</epage><pages>373-383</pages><issn>0378-4320</issn><eissn>1873-2232</eissn><abstract><![CDATA[In the present study we characterize the developmental potential of prepubertal and adult ovine oocytes, analyzing the developmental speed to two-cell and blastocyst stages and its relationship with hatching from the zona pellucida, development after vitrification and the number and allocation of inner mass and trophoblastic cells. Prepubertal and adult ovine oocytes were matured and fertilized in vitro and first cleavage rates at 22, 26 and 32
h were recorded. Cleaved oocytes were cultured and blastocyst production was assessed at 6–9 days post-fertilization (dpf). Blastocysts from the two sources obtained on different days were divided into two groups: the first was vitrified, warmed and cultured in vitro to evaluate re-expansion of the blastocoelic cavity; blastocysts of the second were cultured separately to allow for hatching and count of trophoblastic and inner mass cells of hatched blastocysts by differential staining. We observed a significantly lower rate (
P
<
0.01) of cleaved prepubertal oocytes at 22 and 26
h after fertilization while it was higher (
P
<
0.01) at 32
h than in the adult ones. Adult blastocyst production was significantly lower (
P
<
0.01) in prepubertal than in adult groups and began on the seventh dpf, later (
P
<
0.01) than in the adult group, where they appeared on the sixth dpf. Prepubertal blastocysts hatched at a lower rate than the adult ones (
P
<
0.01) and in both experimental groups faster blastocysts showed a higher (
P
<
0.01) hatching rate. Similarly, prepubertal derived blastocysts showed lower viability after vitrification (
P
<
0.01) compared to the adult counterparts, and in particular slower embryos had reduced viability after vitrification compared to the fastest (
P
<
0.01). Cell number was not different between blastocysts of both groups obtained at 6 and 7
dpf, which were higher (
P
<
0.01) than those obtained at 8 and 9
dpf. The ICM/trophoblast cell ratio was similar in 6- and 7-day obtained blastocyst and increased (
P
<
0.01) in those obtained 1 or 2 days later. These findings show that differences in kinetic development between prepubertal and adult derived embryos reflect differences in developmental capacity of the oocytes from which they derive and could be indicative of embryo quality.]]></abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>16054784</pmid><doi>10.1016/j.anireprosci.2005.05.027</doi><tpages>11</tpages></addata></record> |
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language | eng |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Animals blastocyst Blastocyst - physiology cell culture Cell Division Cleavage Stage, Ovum - physiology embryo (animal) Embryo Culture Techniques - veterinary embryogenesis Embryonic Development - physiology ewes Female Fertilization in Vitro - veterinary Kinetics Kinetics cleavage Male Oocyte oocytes Ovine Prepubertal Sexual Maturation - physiology Sheep - embryology Time Factors tissue culture trophoblast viability vitrification vitrified oocysts zona pellucida |
title | Delay on the in vitro kinetic development of prepubertal ovine embryos |
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