Involvement of the cytoskeleton in the movement of cortical granules during oocyte maturation, and cortical granule anchoring in mouse eggs

被引:80
作者
Connors, SA
Kanatsu-Shinohara, M
Schultz, RM
Kopf, GS
机构
[1] Univ Penn, Ctr Res Reprod & Womens Hlth, Dept Obstet & Gynecol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
关键词
mouse; oocyte; egg; cortical granule; exocytosis; microfilaments; microtubules; cortical granule-free domain;
D O I
10.1006/dbio.1998.8945
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Exocytosis of cortical granules in mouse eggs is required to produce the zona pellucida block to polyspermy. In this study, we examined the role of microfilaments and microtubules in the regulation of cortical granule movement toward the cortex during oocyte maturation and anchoring of cortical granules in the cortex. Fluorescently labeled cortical granules, microfilaments, and microtubules were visualized using laser-scanning confocal microscopy. It was observed that cortical granules migrate to the periphery of the oocyte during oocyte maturation. This movement is blocked by the treatment of oocytes with cytochalasin D, an inhibitor of microfilament polymerization, but not with nocodazole or colchicine, inhibitors of microtubule polymerization. Cortical granules, once anchored at the cortex, remained in the cortex following treatment of metaphase II-arrested eggs with each of these inhibitors; i.e., there was neither inward movement nor precocious exocytosis. Finally, the single cortical granule-free domain that normally becomes localized over the metaphase II spindle was not observed when the chromosomes become scattered following microtubule disruption with nocodazole or colchicine. In these instances a cortical granule-free domain was observed over each individual chromosome, suggesting that the chromosome or chromosome-associated material, and not the spindle, dictates the localization of the cortical granule-free domain. (C) 1998 Academic Press.
引用
收藏
页码:103 / 115
页数:13
相关论文
共 36 条
[1]   MATURE DOMESTIC CAT OOCYTE DOES NOT EXPRESS A CORTICAL GRANULE-FREE DOMAIN [J].
BYERS, AP ;
BARONE, MA ;
DONOGHUE, AM ;
WILDT, DE .
BIOLOGY OF REPRODUCTION, 1992, 47 (05) :709-715
[2]   DEPHOSPHORYLATED SYNAPSIN-I ANCHORS SYNAPTIC VESICLES TO ACTIN CYTOSKELETON - AN ANALYSIS BY VIDEOMICROSCOPY [J].
CECCALDI, PE ;
GROHOVAZ, F ;
BENFENATI, F ;
CHIEREGATTI, E ;
GREENGARD, P ;
VALTORTA, F .
JOURNAL OF CELL BIOLOGY, 1995, 128 (05) :905-912
[3]  
CHATOT CL, 1989, J REPROD FERTIL, V86, P679, DOI 10.1530/jrf.0.0860679
[4]  
Conner S, 1997, MOL REPROD DEV, V48, P106
[5]   CHANGES IN THE DISTRIBUTION OF MOUSE OOCYTE CORTICAL GRANULES AND ABILITY TO UNDERGO THE CORTICAL REACTION DURING GONADOTROPIN-STIMULATED MEIOTIC MATURATION AND AGING INVIVO [J].
DUCIBELLA, T ;
DUFFY, P ;
REINDOLLAR, R ;
SU, B .
BIOLOGY OF REPRODUCTION, 1990, 43 (05) :870-876
[6]   THE DEVELOPMENT OF MOUSE OOCYTE CORTICAL REACTION COMPETENCE IS ACCOMPANIED BY MAJOR CHANGES IN CORTICAL VESICLES AND NOT CORTICAL GRANULE DEPTH [J].
DUCIBELLA, T ;
RANGARAJAN, S ;
ANDERSON, E .
DEVELOPMENTAL BIOLOGY, 1988, 130 (02) :789-792
[7]   QUANTIFICATION AND LOCALIZATION OF CORTICAL GRANULES DURING OOGENESIS IN THE MOUSE [J].
DUCIBELLA, T ;
DUFFY, P ;
BUETOW, J .
BIOLOGY OF REPRODUCTION, 1994, 50 (03) :467-473
[8]   PRECOCIOUS LOSS OF CORTICAL GRANULES DURING MOUSE OOCYTE MEIOTIC MATURATION AND CORRELATION WITH AN EGG-INDUCED MODIFICATION OF THE ZONA PELLUCIDA [J].
DUCIBELLA, T ;
KURASAWA, S ;
RANGARAJAN, S ;
KOPF, GS ;
SCHULTZ, RM .
DEVELOPMENTAL BIOLOGY, 1990, 137 (01) :46-55
[9]   QUANTITATIVE STUDIES OF CHANGES IN CORTICAL GRANULE NUMBER AND DISTRIBUTION IN THE MOUSE OOCYTE DURING MEIOTIC MATURATION [J].
DUCIBELLA, T ;
ANDERSON, E ;
ALBERTINI, DF ;
AALBERG, J ;
RANGARAJAN, S .
DEVELOPMENTAL BIOLOGY, 1988, 130 (01) :184-197
[10]   COMPETENCE TO UNDERGO NORMAL, FERTILIZATION-INDUCED CORTICAL ACTIVATION DEVELOPS AFTER METAPHASE-I OF MEIOSIS IN MOUSE OOCYTES [J].
DUCIBELLA, T ;
BUETOW, J .
DEVELOPMENTAL BIOLOGY, 1994, 165 (01) :95-104