Biochemical and Developmental Evidence That Ooplasmic Maturation of Prepubertal Bovine Oocytes Is Compromised

Our previous studies have shown that oocytes collected from prepubertal calves lack developmental competence. The overall objective of this study was to assess causes by comparing biochemical and physiologic changes during in vitro maturation of oocytes collected from ovaries of adult cattle at slau...

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Veröffentlicht in:Biology of reproduction 2001-06, Vol.64 (6), p.1761-1768
Hauptverfasser: SALAMONE, D. F, DAMIANI, P, FISSORE, R. A, ROBL, J. M, DUBY, R. T
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container_end_page 1768
container_issue 6
container_start_page 1761
container_title Biology of reproduction
container_volume 64
creator SALAMONE, D. F
DAMIANI, P
FISSORE, R. A
ROBL, J. M
DUBY, R. T
description Our previous studies have shown that oocytes collected from prepubertal calves lack developmental competence. The overall objective of this study was to assess causes by comparing biochemical and physiologic changes during in vitro maturation of oocytes collected from ovaries of adult cattle at slaughter and from superstimulated calves (
doi_str_mv 10.1095/biolreprod64.6.1761
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The activities of MPF and MAPK and the relative amount of IP 3 R were significantly lower in calf oocytes. The physiologic significance of these observations was determined by assessing the developmental potential of embryos derived by reciprocal transfer of metaphase II (M-II) chromosomes between cow and calf ooplasts and transfer of adult cumulus cells (G0/G1) into cow and calf ooplasts. Procedural controls consisted of transfer of M-II between adult oocytes and parthenogenic activation of adult and calf oocytes. Adult parthenogenically activated oocytes cleaved and developed to blastocysts at a higher rate than did similarly activated calf oocytes (42.1% vs. 3.4%, P &lt; 0.05). Cleavage was also higher in reciprocal M-II transfer embryos containing adult ooplasm (46.2% vs. 12.0%, P &lt; 0.05). Cleavage (66.7% vs. 21.9%, P &lt; 0.05) and development to blastocyst (20.1% vs. 4.8%, P &lt; 0.05) of nuclear transfer embryos reconstructed from adult cumulus cells was higher after transfer to adult ooplasts. Collectively, these results support the hypothesis that lack of developmental competence of calf oocytes is due to their failure or inability to complete ooplasmic maturation.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod64.6.1761</identifier><identifier>PMID: 11369606</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>Aging ; Animals ; Biological and medical sciences ; Blastocyst - physiology ; Blotting, Western ; Calcium Channels - analysis ; Cattle - growth &amp; development ; Cleavage Stage, Ovum ; Cytoplasm - physiology ; Female ; Fundamental and applied biological sciences. Psychology ; Inositol 1,4,5-Trisphosphate Receptors ; Mammalian female genital system ; Maturation-Promoting Factor - analysis ; Mitogen-Activated Protein Kinases - analysis ; Morphology. 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F</creatorcontrib><creatorcontrib>DAMIANI, P</creatorcontrib><creatorcontrib>FISSORE, R. A</creatorcontrib><creatorcontrib>ROBL, J. M</creatorcontrib><creatorcontrib>DUBY, R. T</creatorcontrib><title>Biochemical and Developmental Evidence That Ooplasmic Maturation of Prepubertal Bovine Oocytes Is Compromised</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>Our previous studies have shown that oocytes collected from prepubertal calves lack developmental competence. The overall objective of this study was to assess causes by comparing biochemical and physiologic changes during in vitro maturation of oocytes collected from ovaries of adult cattle at slaughter and from superstimulated calves (&lt;6 mo old) by either laporotomy or ultrasound-guided follicular aspiration. Activity and/or concentrations of maturation-promoting factor (MPF), mitogen-activated protein kinase (MAPK), and inositol 1,4,5-trisphosphate receptor (IP 3 R) were determined by measuring phosphorylation of histone H-1 kinase, phosphorylation of myelin basic protein, or Western blotting, respectively, and were compared between oocytes collected from calves and for those collected from cows. The activities of MPF and MAPK and the relative amount of IP 3 R were significantly lower in calf oocytes. The physiologic significance of these observations was determined by assessing the developmental potential of embryos derived by reciprocal transfer of metaphase II (M-II) chromosomes between cow and calf ooplasts and transfer of adult cumulus cells (G0/G1) into cow and calf ooplasts. Procedural controls consisted of transfer of M-II between adult oocytes and parthenogenic activation of adult and calf oocytes. Adult parthenogenically activated oocytes cleaved and developed to blastocysts at a higher rate than did similarly activated calf oocytes (42.1% vs. 3.4%, P &lt; 0.05). Cleavage was also higher in reciprocal M-II transfer embryos containing adult ooplasm (46.2% vs. 12.0%, P &lt; 0.05). Cleavage (66.7% vs. 21.9%, P &lt; 0.05) and development to blastocyst (20.1% vs. 4.8%, P &lt; 0.05) of nuclear transfer embryos reconstructed from adult cumulus cells was higher after transfer to adult ooplasts. Collectively, these results support the hypothesis that lack of developmental competence of calf oocytes is due to their failure or inability to complete ooplasmic maturation.</description><subject>Aging</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blastocyst - physiology</subject><subject>Blotting, Western</subject><subject>Calcium Channels - analysis</subject><subject>Cattle - growth &amp; development</subject><subject>Cleavage Stage, Ovum</subject><subject>Cytoplasm - physiology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Inositol 1,4,5-Trisphosphate Receptors</subject><subject>Mammalian female genital system</subject><subject>Maturation-Promoting Factor - analysis</subject><subject>Mitogen-Activated Protein Kinases - analysis</subject><subject>Morphology. Physiology</subject><subject>Myelin Basic Protein - metabolism</subject><subject>Nuclear Transfer Techniques</subject><subject>Oocytes - chemistry</subject><subject>Oocytes - physiology</subject><subject>Oocytes - ultrastructure</subject><subject>Phosphorylation</subject><subject>Protein Kinases - metabolism</subject><subject>Receptors, Cytoplasmic and Nuclear - analysis</subject><subject>Sexual Maturation</subject><subject>Vertebrates: reproduction</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc1O6zAQhS0Egt7CEyAhLxC7FP_FTpZQ4F4kECxgHTn2hBg5cYmTVrw9riiX1Uijb845OoPQKSULSsr8snbBD7AagpViIRdUSbqHZjRnZaaYLPbRjBAiM84lP0J_YnwnhArO-CE6opTLUhI5Q921C6aFzhntse4tvoE1-LDqoB_T5nbtLPQG8EurR_wUVl7HxOJHPU6DHl3ocWjwc4ox1TBsL67D2vWQUPM5QsT3ES9Dl0J2LoI9RgeN9hFOdnOOXu9uX5b_soenv_fLq4esZVKNGc0VWJbz2uSGSV4KBYwRWYqmKQqlmlqzotQ1VxRYU5RWCKJYXRQWiBHGlnyOLr51k_HHBHGskr0B73UPYYqVIoWS2y7m6GwHTnUHtloNrtPDZ_VTUALOd4COqaJm0L1x8ZdLQiIl_W_Yurd24waoYqe9T6q82mw2UlSy2j6IfwGC84U9</recordid><startdate>20010601</startdate><enddate>20010601</enddate><creator>SALAMONE, D. 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Physiology</topic><topic>Myelin Basic Protein - metabolism</topic><topic>Nuclear Transfer Techniques</topic><topic>Oocytes - chemistry</topic><topic>Oocytes - physiology</topic><topic>Oocytes - ultrastructure</topic><topic>Phosphorylation</topic><topic>Protein Kinases - metabolism</topic><topic>Receptors, Cytoplasmic and Nuclear - analysis</topic><topic>Sexual Maturation</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SALAMONE, D. F</creatorcontrib><creatorcontrib>DAMIANI, P</creatorcontrib><creatorcontrib>FISSORE, R. A</creatorcontrib><creatorcontrib>ROBL, J. M</creatorcontrib><creatorcontrib>DUBY, R. 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T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biochemical and Developmental Evidence That Ooplasmic Maturation of Prepubertal Bovine Oocytes Is Compromised</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2001-06-01</date><risdate>2001</risdate><volume>64</volume><issue>6</issue><spage>1761</spage><epage>1768</epage><pages>1761-1768</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>Our previous studies have shown that oocytes collected from prepubertal calves lack developmental competence. The overall objective of this study was to assess causes by comparing biochemical and physiologic changes during in vitro maturation of oocytes collected from ovaries of adult cattle at slaughter and from superstimulated calves (&lt;6 mo old) by either laporotomy or ultrasound-guided follicular aspiration. Activity and/or concentrations of maturation-promoting factor (MPF), mitogen-activated protein kinase (MAPK), and inositol 1,4,5-trisphosphate receptor (IP 3 R) were determined by measuring phosphorylation of histone H-1 kinase, phosphorylation of myelin basic protein, or Western blotting, respectively, and were compared between oocytes collected from calves and for those collected from cows. The activities of MPF and MAPK and the relative amount of IP 3 R were significantly lower in calf oocytes. The physiologic significance of these observations was determined by assessing the developmental potential of embryos derived by reciprocal transfer of metaphase II (M-II) chromosomes between cow and calf ooplasts and transfer of adult cumulus cells (G0/G1) into cow and calf ooplasts. Procedural controls consisted of transfer of M-II between adult oocytes and parthenogenic activation of adult and calf oocytes. Adult parthenogenically activated oocytes cleaved and developed to blastocysts at a higher rate than did similarly activated calf oocytes (42.1% vs. 3.4%, P &lt; 0.05). Cleavage was also higher in reciprocal M-II transfer embryos containing adult ooplasm (46.2% vs. 12.0%, P &lt; 0.05). Cleavage (66.7% vs. 21.9%, P &lt; 0.05) and development to blastocyst (20.1% vs. 4.8%, P &lt; 0.05) of nuclear transfer embryos reconstructed from adult cumulus cells was higher after transfer to adult ooplasts. Collectively, these results support the hypothesis that lack of developmental competence of calf oocytes is due to their failure or inability to complete ooplasmic maturation.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>11369606</pmid><doi>10.1095/biolreprod64.6.1761</doi><tpages>8</tpages></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; BioOne Complete
subjects Aging
Animals
Biological and medical sciences
Blastocyst - physiology
Blotting, Western
Calcium Channels - analysis
Cattle - growth & development
Cleavage Stage, Ovum
Cytoplasm - physiology
Female
Fundamental and applied biological sciences. Psychology
Inositol 1,4,5-Trisphosphate Receptors
Mammalian female genital system
Maturation-Promoting Factor - analysis
Mitogen-Activated Protein Kinases - analysis
Morphology. Physiology
Myelin Basic Protein - metabolism
Nuclear Transfer Techniques
Oocytes - chemistry
Oocytes - physiology
Oocytes - ultrastructure
Phosphorylation
Protein Kinases - metabolism
Receptors, Cytoplasmic and Nuclear - analysis
Sexual Maturation
Vertebrates: reproduction
title Biochemical and Developmental Evidence That Ooplasmic Maturation of Prepubertal Bovine Oocytes Is Compromised
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