Literature DB >> 2744234

In vitro and in vivo studies reveal that hamster oocyte meiotic arrest is maintained only transiently by follicular fluid, but persistently by membrana/cumulus granulosa cell contact.

C Racowsky1, K V Baldwin.   

Abstract

Studies were carried out with the golden Syrian hamster to investigate the capacity of follicular fluid to maintain oocyte meiotic arrest and to determine the importance of cumulus-membrana granulosa cell contact in the regulation of meiotic status. The follicular fluid studies were conducted by cytological assessment of meiotic stage up to 6 hr after transferring cumulus-free oocytes into antra of explanted "host" follicles in vitro or into follicles of anesthetized animals prior to the gonadotropin surge at proestrus in vivo. The cumulus-membrana granulosa contact studies were undertaken with explanted follicles in which the oocyte-cumulus complex was dislodged from the underlying membrana granulosa, released into the antrum, and subsequently allowed to reestablish contact during 6 hr of incubation within the follicle. The extent of recontact of the dislodged complex with the underlying membrana granulosa was assessed visually at the end of incubation and was classified as close, moderate, or none. These various degrees of contact typically involved the following number of cumulus cells, as determined by serial sectioning of a representative sample of follicles after dislodgement and subsequent incubation: close, 32.7 +/- 1.78; moderate, 9.0 +/- 2.1; and no contact, 0. After 6 hr of incubation either in vitro or in vivo, few transferred oocytes remained at the germinal vesicle (GV) stage (18.8 +/- 8.7 and 17.3 +/- 4.0% GV, respectively). However, time course experiments revealed that meiotic resumption was significantly delayed in transferred oocytes compared with either liberated oocytes, spontaneously maturing oocytes, or follicle-enclosed oocytes induced to mature by luteinizing hormone in vitro (after 4 hr, transferred, 31.3 +/- 6.0% GV; liberated, 0% GV; follicle-enclosed, 0% GV; after 6 hr, 0% transferred oocytes exhibited a GV). In the dislodgement studies, after 6 hr of incubation, 26% of complexes reestablished close contact with the underlying membrana granulosa, 67% showed moderate contact, while 7% revealed no contact. There was a significant increase in the percentage GV stage oocytes as the extent of recontact increased (no contact, 21.9 +/- 3.6% GV; moderate contact, 56.6 +/- 6.8% GV; close contact, 87.5 +/- 14.4% GV). These data argue in favor of a stringent control of hamster oocyte meiotic status by the follicle cell/oocyte syncytium and against the possibility that follicular fluid is independently responsible for maintaining meiotic arrest.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1989        PMID: 2744234     DOI: 10.1016/0012-1606(89)90102-4

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  10 in total

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Review 2.  Hormonal control of mammalian oocyte meiosis at diplotene stage.

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Journal:  J Assist Reprod Genet       Date:  1998-03       Impact factor: 3.412

Review 4.  Regulation of Mammalian Oocyte Meiosis by Intercellular Communication Within the Ovarian Follicle.

Authors:  Laurinda A Jaffe; Jeremy R Egbert
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5.  Luteinizing hormone reduces the activity of the NPR2 guanylyl cyclase in mouse ovarian follicles, contributing to the cyclic GMP decrease that promotes resumption of meiosis in oocytes.

Authors:  Jerid W Robinson; Meijia Zhang; Leia C Shuhaibar; Rachael P Norris; Andreas Geerts; Frank Wunder; John J Eppig; Lincoln R Potter; Laurinda A Jaffe
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Review 6.  Regulation of germ cell development by intercellular signaling in the mammalian ovarian follicle.

Authors:  Hugh J Clarke
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7.  Luteinizing hormone causes MAP kinase-dependent phosphorylation and closure of connexin 43 gap junctions in mouse ovarian follicles: one of two paths to meiotic resumption.

Authors:  Rachael P Norris; Marina Freudzon; Lisa M Mehlmann; Ann E Cowan; Alexander M Simon; David L Paul; Paul D Lampe; Laurinda A Jaffe
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8.  Meiotic arrest in human oocytes is maintained by a Gs signaling pathway.

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9.  Regulation of meiotic prophase arrest in mouse oocytes by GPR3, a constitutive activator of the Gs G protein.

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Journal:  J Cell Biol       Date:  2005-10-24       Impact factor: 10.539

Review 10.  Selective Regulation of Oocyte Meiotic Events Enhances Progress in Fertility Preservation Methods.

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Journal:  Biochem Insights       Date:  2015-09-20
  10 in total

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