CHANGES IN GAP JUNCTION CONNEXIN-43 MESSENGER-RIBONUCLEIC-ACID LEVELSASSOCIATED WITH RAT OVARIAN FOLLICULAR DEVELOPMENT AS DEMONSTRATED BYINSITU HYBRIDIZATION

Citation
Jr. Schreiber et al., CHANGES IN GAP JUNCTION CONNEXIN-43 MESSENGER-RIBONUCLEIC-ACID LEVELSASSOCIATED WITH RAT OVARIAN FOLLICULAR DEVELOPMENT AS DEMONSTRATED BYINSITU HYBRIDIZATION, American journal of obstetrics and gynecology, 168(4), 1993, pp. 1094-1104
Citations number
22
Categorie Soggetti
Obsetric & Gynecology
ISSN journal
00029378
Volume
168
Issue
4
Year of publication
1993
Pages
1094 - 1104
Database
ISI
SICI code
0002-9378(1993)168:4<1094:CIGJCM>2.0.ZU;2-O
Abstract
OBJECTIVE: The purpose was to evaluate the changes in gap junction con nexin-43 messenger ribonucleic acid levels associated with rat ovarian follicular development. Gap junctions connect the plasma membranes of adjacent cells through cell-to-cell channels, allowing synchronizatio n of cellular events, including ovarian follicular development. Ovaria n gap junctions consist of the protein connexin-43. STUDY DESIGN: We u sed the hypophysectomized immature rat treated with estrogen or gonado tropins as a model to study the ovarian regulation of connexin-43 mess enger ribonucleic acid. In situ hybridization with radiolabeled ribopr obes was used to localize and quantitate connexin-43 messenger ribonuc leic acid. RESULTS: We demonstrated that connexin-43 messenger ribonuc leic acid was localized to follicular granulosa cells. Estrogen signif icantly up-regulated connexin-43 messenger ribonucleic acid (91%), whe reas gonadotropins that stimulate ovulation and corpus luteum formatio n completely down-regulated the connexin-43 gene. These results correl ate closely with previous immunohistochemical studies of connexin-43 p rotein. CONCLUSION: The positive correlation between follicular develo pment and granulosa cell content of connexin-43 messenger ribonucleic acid is caused by transcriptional activation of the gap junction conne xin-43 gene, posttranscriptional stability of connexin-43 messenger ri bonucleic acid, or both. Future studies will determine the molecular m echanisms of hormonal regulation of the connexin-43 gene.