Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
2000-12-1
pubmed:abstractText
The functions of estrogen receptors (ERs) in mouse ovary and genital tracts were investigated by generating null mutants for ERalpha (ERalphaKO), ERbeta (ERbetaKO) and both ERs (ERalphabetaKO). All ERalphaKO females are sterile, whereas ERbetaKO females are either infertile or exhibit variable degrees of subfertility. Mast cells present in adult ERalphaKO and ERalphabetaKO ovaries could participate in the generation of hemorrhagic cysts. Folliculogenesis proceeds normally up to the large antral stage in both ERalphaKO and ERbetaKO adults, whereas large antral follicles of ERalpha+/-ERbetaKO and ERalphabetaKO adults are markedly deficient in granulosa cells. Similarly, prematurely developed follicles found in prepubertal ERalphaKO ovaries appear normal, but their ERalphabetaKO counterparts display only few granulosa cell layers. Upon superovulation treatment, all prepubertal ERalphaKO females form numerous preovulatory follicles of which the vast majority do not ovulate. The same treatment fails to elicit the formation of preovulatory follicles in half of the ERbetaKO mice and in all ERalpha+/-/ERbetaKO mice. These and other results reveal a functional redundancy between ERalpha and ERbeta for ovarian folliculogenesis, and strongly suggest that (1) ERbeta plays an important role in mediating the stimulatory effects of estrogens on granulosa cell proliferation, (2) ERalpha is not required for follicle growth under wild type conditions, while it is indispensable for ovulation, and (3) ERalpha is also necessary for interstitial glandular cell development. Our data also indicate that ERbeta exerts some function in ERalphaKO uterus and vagina. ERalphabetaKO granulosa cells localized within degenerating follicles transform into cells displaying junctions that are unique to testicular Sertoli cells. From the distribution pattern of anti-Müllerian hormone (AMH) in ERalphabetaKO ovaries, it is unlikely that an elevated AMH level is the cause of Sertoli cell differentiation. Our results also show that cell proliferation in the prostate and urinary bladder of old ERbetaKO and ERalphabetaKO males is apparently normal.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0950-1991
pubmed:author
pubmed:issnType
Print
pubmed:volume
127
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4277-91
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:10976058-Animals, pubmed-meshheading:10976058-Anti-Mullerian Hormone, pubmed-meshheading:10976058-Cysts, pubmed-meshheading:10976058-Estrogen Receptor alpha, pubmed-meshheading:10976058-Estrogen Receptor beta, pubmed-meshheading:10976058-Female, pubmed-meshheading:10976058-Fertility, pubmed-meshheading:10976058-Genitalia, Female, pubmed-meshheading:10976058-Genitalia, Male, pubmed-meshheading:10976058-Glycoproteins, pubmed-meshheading:10976058-Gonadotropins, pubmed-meshheading:10976058-Growth Inhibitors, pubmed-meshheading:10976058-Infertility, Female, pubmed-meshheading:10976058-Intercellular Junctions, pubmed-meshheading:10976058-Male, pubmed-meshheading:10976058-Mast Cells, pubmed-meshheading:10976058-Mice, pubmed-meshheading:10976058-Mice, Knockout, pubmed-meshheading:10976058-Ovarian Follicle, pubmed-meshheading:10976058-Ovary, pubmed-meshheading:10976058-Ovulation, pubmed-meshheading:10976058-Phenotype, pubmed-meshheading:10976058-Receptors, Estrogen, pubmed-meshheading:10976058-Sertoli Cells, pubmed-meshheading:10976058-Sexual Maturation, pubmed-meshheading:10976058-Testicular Hormones
pubmed:year
2000
pubmed:articleTitle
Effect of single and compound knockouts of estrogen receptors alpha (ERalpha) and beta (ERbeta) on mouse reproductive phenotypes.
pubmed:affiliation
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, Collège de France, BP 163, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't