Author:
Findlay J. K.,Britt K.,Kerr J. B.,O'Donnell L.,Jones M. E.,Drummond A. E.,Simpson E. R.
Abstract
Oestrogens have been known for many years to have a direct influence on
folliculogenesis. Oestradiol-17β‚ (E2) and its analogues have both
proliferative and differentiative effects on somatic cells of follicles.
Nevertheless, definitive proof of an obligatory role for oestrogen in
folliculogenesis and elucidation of the mechanisms subserving its different
actions in follicular cells remains elusive. Several recent developments
permit a re-examination of the roles and actions of E2 in the follicle. They
are: (i) the discovery of a second form of the oestrogen
receptor, ERβ; (ii) the advent of genetically
modified mice with deletions in the ERα(αERKO) ERβ‚
BERKO) and the double ER deletions (αβERKO); and
(iii) a mouse model of oestrogen deficiency (ArKO) by
targeted disruption of the cyp
19gene encoding the aromatase enzyme. Recent information
derived from these models is reviewed to re-assess the roles and actions of
oestrogens in follicular dynamics and the phenotypic differentiation of
ovarian somatic cells in the ovary. The data demonstrate that oestrogen is
obligatory for normal folliculogenesis and that the phenotype of the ovarian
somatic cells depends on the steroid milieu. The ArKO mouse provides a model
to test the roles of the respective ERs in proliferation and differentiation
using specific agonists and antagonists, and to study regulation of the
differentiation of ovarian and testicular somatic cells.
Subject
Developmental Biology,Endocrinology,Genetics,Molecular Biology,Animal Science and Zoology,Reproductive Medicine,Biotechnology
Cited by
54 articles.
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