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The Role of Microfilaments in Early Meiotic Maturation of Mouse Oocytes
Mouse oocyte microfilaments (MF) were perturbed by depolymerization (cytochalasin B) or stabilization (jasplakinolide) and correlated meiotic defects examined by confocal microscopy. MF, microtubules, and mitochondria were vitally stained; centrosomes (γ-tubulin), after fixation. MF depolymerization...
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Published in: | Microscopy and microanalysis 2005-04, Vol.11 (2), p.146-153 |
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description | Mouse oocyte microfilaments (MF) were perturbed by depolymerization
(cytochalasin B) or stabilization (jasplakinolide) and correlated
meiotic defects examined by confocal microscopy. MF, microtubules, and
mitochondria were vitally stained; centrosomes (γ-tubulin), after
fixation. MF depolymerization by cytochalasin in culture medium did not
affect central migration of centrosomes, mitochondria, or nuclear
breakdown (GVBD); some MF signal was localized around the germinal
vesicle (GV). In maturation-blocking medium (containing IBMX), central
movement was curtailed and cortical MF aggregations made the plasma
membrane wavy. Occasional long MF suggested that not all MF were
depolymerized. MF stabilization by jasplakinolide led to MF
aggregations throughout the cytoplasm. GVBD occurred (unless IBMX was
present) but no spindle formed. Over time, most oocytes constricted
creating a dumbbell shape with MF concentrated under one-half of the
oocyte cortex and on either side of the constriction. In IBMX medium,
the MF-containing half of the dumbbell over time sequestered the GV,
MF, mitochondria, and one to two large cortical centrosomes; the non-MF
half appeared empty. Cumulus processes contacted the oocyte surface
(detected by microtubule content) and mirrored MF distribution. Results
demonstrated that MF play an essential role in meiosis, primarily
through cortically mediated events, including centrosome localization,
spindle (or GV) movement to the periphery, activation of (polar body)
constriction, and establishment of oocyte polarity. The presence of a
cortical “organizing pole” is hypothesized. |
doi_str_mv | 10.1017/S1431927605050154 |
format | article |
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(cytochalasin B) or stabilization (jasplakinolide) and correlated
meiotic defects examined by confocal microscopy. MF, microtubules, and
mitochondria were vitally stained; centrosomes (γ-tubulin), after
fixation. MF depolymerization by cytochalasin in culture medium did not
affect central migration of centrosomes, mitochondria, or nuclear
breakdown (GVBD); some MF signal was localized around the germinal
vesicle (GV). In maturation-blocking medium (containing IBMX), central
movement was curtailed and cortical MF aggregations made the plasma
membrane wavy. Occasional long MF suggested that not all MF were
depolymerized. MF stabilization by jasplakinolide led to MF
aggregations throughout the cytoplasm. GVBD occurred (unless IBMX was
present) but no spindle formed. Over time, most oocytes constricted
creating a dumbbell shape with MF concentrated under one-half of the
oocyte cortex and on either side of the constriction. In IBMX medium,
the MF-containing half of the dumbbell over time sequestered the GV,
MF, mitochondria, and one to two large cortical centrosomes; the non-MF
half appeared empty. Cumulus processes contacted the oocyte surface
(detected by microtubule content) and mirrored MF distribution. Results
demonstrated that MF play an essential role in meiosis, primarily
through cortically mediated events, including centrosome localization,
spindle (or GV) movement to the periphery, activation of (polar body)
constriction, and establishment of oocyte polarity. The presence of a
cortical “organizing pole” is hypothesized.</description><identifier>ISSN: 1431-9276</identifier><identifier>EISSN: 1435-8115</identifier><identifier>DOI: 10.1017/S1431927605050154</identifier><identifier>PMID: 15817144</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><subject>1-Methyl-3-isobutylxanthine ; Actin Cytoskeleton - physiology ; Actin Cytoskeleton - ultrastructure ; Animals ; BIOLOGICAL APPLICATIONS ; Cells ; Cells, Cultured ; Meiosis ; Mice ; Mice, Inbred ICR ; Microscopy ; Oocytes - cytology ; Oocytes - ultrastructure ; Plasma ; Proteins ; Staining and Labeling ; Studies</subject><ispartof>Microscopy and microanalysis, 2005-04, Vol.11 (2), p.146-153</ispartof><rights>2005 Microscopy Society of America</rights><rights>Copyright Cambridge University Press Apr 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-d0653b6724f3a0678462ea66b27f8c84e3ca254f915438715e7a28ca03368d53</citedby><cites>FETCH-LOGICAL-c465t-d0653b6724f3a0678462ea66b27f8c84e3ca254f915438715e7a28ca03368d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S1431927605050154/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,72730</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15817144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Calarco, Patricia G.</creatorcontrib><title>The Role of Microfilaments in Early Meiotic Maturation of Mouse Oocytes</title><title>Microscopy and microanalysis</title><addtitle>Microsc Microanal</addtitle><description>Mouse oocyte microfilaments (MF) were perturbed by depolymerization
(cytochalasin B) or stabilization (jasplakinolide) and correlated
meiotic defects examined by confocal microscopy. MF, microtubules, and
mitochondria were vitally stained; centrosomes (γ-tubulin), after
fixation. MF depolymerization by cytochalasin in culture medium did not
affect central migration of centrosomes, mitochondria, or nuclear
breakdown (GVBD); some MF signal was localized around the germinal
vesicle (GV). In maturation-blocking medium (containing IBMX), central
movement was curtailed and cortical MF aggregations made the plasma
membrane wavy. Occasional long MF suggested that not all MF were
depolymerized. MF stabilization by jasplakinolide led to MF
aggregations throughout the cytoplasm. GVBD occurred (unless IBMX was
present) but no spindle formed. Over time, most oocytes constricted
creating a dumbbell shape with MF concentrated under one-half of the
oocyte cortex and on either side of the constriction. In IBMX medium,
the MF-containing half of the dumbbell over time sequestered the GV,
MF, mitochondria, and one to two large cortical centrosomes; the non-MF
half appeared empty. Cumulus processes contacted the oocyte surface
(detected by microtubule content) and mirrored MF distribution. Results
demonstrated that MF play an essential role in meiosis, primarily
through cortically mediated events, including centrosome localization,
spindle (or GV) movement to the periphery, activation of (polar body)
constriction, and establishment of oocyte polarity. The presence of a
cortical “organizing pole” is hypothesized.</description><subject>1-Methyl-3-isobutylxanthine</subject><subject>Actin Cytoskeleton - physiology</subject><subject>Actin Cytoskeleton - ultrastructure</subject><subject>Animals</subject><subject>BIOLOGICAL APPLICATIONS</subject><subject>Cells</subject><subject>Cells, Cultured</subject><subject>Meiosis</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Microscopy</subject><subject>Oocytes - cytology</subject><subject>Oocytes - ultrastructure</subject><subject>Plasma</subject><subject>Proteins</subject><subject>Staining and Labeling</subject><subject>Studies</subject><issn>1431-9276</issn><issn>1435-8115</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp1kF9LwzAUxYMobk4_gC9SfPCtmpu_7aOMOYWNge69pG2qGW0zk_Zh395sKwwUycMNub9zcu9B6BbwI2CQTx_AKKRECszDAc7O0Dg88TgB4OeHO8T7_ghdeb_BGFMsxSUaAU9AAmNjNF9_6ejd1jqyVbQ0hbOVqVWj285Hpo1mytW7aKmN7UwRLVXXO9UZ2x5o23sdrWyx67S_RheVqr2-GeoErV9m6-lrvFjN36bPi7hggndxiQWnuZCEVVRhIRMmiFZC5ERWSZEwTQtFOKvSsAxNJHAtFUkKhSkVScnpBD0cbbfOfvfad1ljfKHrWrU6jJMJKSFoZQDvf4Eb27s2jJYRgklKANIAwREKa3vvdJVtnWmU22WAs33C2Z-Eg-ZuMO7zRpcnxRBpAOhgqprcmfJTn77-3_YHLeGCiw</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>Calarco, Patricia G.</creator><general>Cambridge University Press</general><general>Oxford University Press</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>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20050401</creationdate><title>The Role of Microfilaments in Early Meiotic Maturation of Mouse Oocytes</title><author>Calarco, Patricia G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-d0653b6724f3a0678462ea66b27f8c84e3ca254f915438715e7a28ca03368d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>1-Methyl-3-isobutylxanthine</topic><topic>Actin Cytoskeleton - physiology</topic><topic>Actin Cytoskeleton - ultrastructure</topic><topic>Animals</topic><topic>BIOLOGICAL APPLICATIONS</topic><topic>Cells</topic><topic>Cells, Cultured</topic><topic>Meiosis</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Microscopy</topic><topic>Oocytes - cytology</topic><topic>Oocytes - ultrastructure</topic><topic>Plasma</topic><topic>Proteins</topic><topic>Staining and Labeling</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Calarco, Patricia G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Microscopy and microanalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Calarco, Patricia G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Role of Microfilaments in Early Meiotic Maturation of Mouse Oocytes</atitle><jtitle>Microscopy and microanalysis</jtitle><addtitle>Microsc Microanal</addtitle><date>2005-04-01</date><risdate>2005</risdate><volume>11</volume><issue>2</issue><spage>146</spage><epage>153</epage><pages>146-153</pages><issn>1431-9276</issn><eissn>1435-8115</eissn><abstract>Mouse oocyte microfilaments (MF) were perturbed by depolymerization
(cytochalasin B) or stabilization (jasplakinolide) and correlated
meiotic defects examined by confocal microscopy. MF, microtubules, and
mitochondria were vitally stained; centrosomes (γ-tubulin), after
fixation. MF depolymerization by cytochalasin in culture medium did not
affect central migration of centrosomes, mitochondria, or nuclear
breakdown (GVBD); some MF signal was localized around the germinal
vesicle (GV). In maturation-blocking medium (containing IBMX), central
movement was curtailed and cortical MF aggregations made the plasma
membrane wavy. Occasional long MF suggested that not all MF were
depolymerized. MF stabilization by jasplakinolide led to MF
aggregations throughout the cytoplasm. GVBD occurred (unless IBMX was
present) but no spindle formed. Over time, most oocytes constricted
creating a dumbbell shape with MF concentrated under one-half of the
oocyte cortex and on either side of the constriction. In IBMX medium,
the MF-containing half of the dumbbell over time sequestered the GV,
MF, mitochondria, and one to two large cortical centrosomes; the non-MF
half appeared empty. Cumulus processes contacted the oocyte surface
(detected by microtubule content) and mirrored MF distribution. Results
demonstrated that MF play an essential role in meiosis, primarily
through cortically mediated events, including centrosome localization,
spindle (or GV) movement to the periphery, activation of (polar body)
constriction, and establishment of oocyte polarity. The presence of a
cortical “organizing pole” is hypothesized.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><pmid>15817144</pmid><doi>10.1017/S1431927605050154</doi><tpages>8</tpages></addata></record> |
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source | Cambridge Journals Online |
subjects | 1-Methyl-3-isobutylxanthine Actin Cytoskeleton - physiology Actin Cytoskeleton - ultrastructure Animals BIOLOGICAL APPLICATIONS Cells Cells, Cultured Meiosis Mice Mice, Inbred ICR Microscopy Oocytes - cytology Oocytes - ultrastructure Plasma Proteins Staining and Labeling Studies |
title | The Role of Microfilaments in Early Meiotic Maturation of Mouse Oocytes |
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