Literature DB >> 2291919

Changes in the distribution of mouse oocyte cortical granules and ability to undergo the cortical reaction during gonadotropin-stimulated meiotic maturation and aging in vivo.

T Ducibella1, P Duffy, R Reindollar, B Su.   

Abstract

Mouse oocyte cortical granule (CG) activation and distribution were investigated during in vivo meiotic maturation to determine the onset of competence to undergo the cortical reaction, which is considered responsible for the block to polyspermy. In the present study, the resumption of oocyte maturation was stimulated by hCG administration. Competence to undergo the cortical reaction (assessed with calcium ionophore A23187) was undetectable (0% loss) in germinal vesicle-stage oocytes 0.5 h after hCG administration. When germinal vesicle breakdown and metaphase I had taken place (3 and 7 h post hCG, respectively), approximately 30% CG loss was observed. Maximal (A23187-inducible) levels of CG loss, 67% and 72%, were present at 10 and 13 h, respectively, during metaphase II. Cortical granule distribution changed dramatically during metaphase I, polar body formation, metaphase II, and post-ovulatory aging in vivo. A stable metaphase II distribution was present from 13 to 18 h. After 24 and 32 h, 28% and 83% of the eggs, respectively, exhibited major alterations in the cortical distribution of CGs, some of which did not appear to be susceptible to release by A23187. These data support the hypothesis that just before ovulation the egg cortex completes the development of its normal structure and physiological competence, which are maintained for only a brief period of time afterward. The implications are discussed for normal fertilization and polyspermy in mammals, including humans.

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Year:  1990        PMID: 2291919     DOI: 10.1095/biolreprod43.5.870

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  19 in total

1.  Ultrastructural markers of quality are impaired in human metaphase II aged oocytes: a comparison between reproductive and in vitro aging.

Authors:  S Bianchi; G Macchiarelli; G Micara; A Linari; C Boninsegna; C Aragona; G Rossi; S Cecconi; S A Nottola
Journal:  J Assist Reprod Genet       Date:  2015-08-15       Impact factor: 3.412

2.  Prophase I mouse oocytes are deficient in the ability to respond to fertilization by decreasing membrane receptivity to sperm and establishing a membrane block to polyspermy.

Authors:  Cassie A Kryzak; Maia M Moraine; Diane D Kyle; Hyo J Lee; Caelin Cubeñas-Potts; Douglas N Robinson; Janice P Evans
Journal:  Biol Reprod       Date:  2013-08-29       Impact factor: 4.285

3.  Meiotic and developmental competence in mice are compromised following follicle development in vitro using an alginate-based culture system.

Authors:  Monica A Mainigi; Teri Ord; Richard M Schultz
Journal:  Biol Reprod       Date:  2011-04-13       Impact factor: 4.285

4.  Postovulatory aging causes the deterioration of porcine oocytes via induction of oxidative stress.

Authors:  Yilong Miao; Changyin Zhou; Zhaokang Cui; Mianqun Zhang; Xiayan ShiYang; Yajuan Lu; Bo Xiong
Journal:  FASEB J       Date:  2018-01-03       Impact factor: 5.191

5.  Differential expression and functions of cortical myosin IIA and IIB isotypes during meiotic maturation, fertilization, and mitosis in mouse oocytes and embryos.

Authors:  C Simerly; G Nowak; P de Lanerolle; G Schatten
Journal:  Mol Biol Cell       Date:  1998-09       Impact factor: 4.138

6.  Twin pregnancy obtained with frozen-thawed embryos after in vitro maturation in a patient with polycystic ovarian syndrome.

Authors:  P-A Godin; O Gaspard; F Thonon; C Jouan; F Wijzen; M Dubois; J-M Foidart
Journal:  J Assist Reprod Genet       Date:  2003-08       Impact factor: 3.412

7.  Post-ovulatory aging of oocytes disrupts kinase signaling pathways and lysosome biogenesis.

Authors:  Lynda K McGinnis; Steven Pelech; William H Kinsey
Journal:  Mol Reprod Dev       Date:  2014-09-19       Impact factor: 2.609

Review 8.  The biology and dynamics of mammalian cortical granules.

Authors:  Min Liu
Journal:  Reprod Biol Endocrinol       Date:  2011-11-17       Impact factor: 5.211

9.  Biochemical heterogeneity, migration, and pre-fertilization release of mouse oocyte cortical granules.

Authors:  Min Liu; DeAndrea Sims; Patricia Calarco; Prue Talbot
Journal:  Reprod Biol Endocrinol       Date:  2003-11-07       Impact factor: 5.211

10.  SIRT1, 2, 3 protect mouse oocytes from postovulatory aging.

Authors:  Teng Zhang; Yang Zhou; Li Li; Hong-Hui Wang; Xue-Shan Ma; Wei-Ping Qian; Wei Shen; Heide Schatten; Qing-Yuan Sun
Journal:  Aging (Albany NY)       Date:  2016-04       Impact factor: 5.682

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