Estrogen is not directly required for oocyte developmental competence

被引:30
作者
Huynh, K
Jones, G
Thouas, G
Britt, KL
Simpson, ER
Jones, MEE
机构
[1] PHIMR, Clayton, Vic 3168, Australia
[2] Monash Univ, Dept Anat, Clayton, Vic 3800, Australia
[3] Monash Univ, Inst Reprod & Dev, Clayton, Vic 3800, Australia
关键词
cumulus cells; estradiol; gamete biology; in vitro fertilization; oocyte development;
D O I
10.1095/biolreprod.103.022111
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oocyte maturation and ovulation require a coordinated interaction between gonadotrophs, steroid hormones, and growth factors. The extent to which estrogen is required in this process, however, remains unclear. To better understand the role of estrogen in maintaining developmental competence of mammalian oocytes, we studied the Aromatase knockout (ArKO) mouse, which has been genetically engineered to be incapable of synthesizing endogenous estrogen. Previous studies have established that ArKO female mice are anovulatory with ovaries that progressively degenerate, developing hemorrhagic cystic follicles. In young ArKO females, however, apparently healthy follicles and oocytes have been observed. We investigated if these oocytes could be induced to ovulate, then mature, fertilize, and develop in vitro. Following a standard superovulation protocol, ArKO oocytes did not ovulate. When recovered manually from the ovary, however, ArKO oocytes successfully progressed through in vitro maturation, fertilization, and development to the blastocyst stage at the same rate as wild-type and heterozygote littermates. Therefore, it appears that estrogen is not required for the production and growth of oocytes capable of maturation and complete preimplantation development but is required for continued follicle growth and feedback regulation of ovulation.
引用
收藏
页码:1263 / 1269
页数:7
相关论文
共 44 条
[1]   ENDOCRINOLOGY OF THE OVARY [J].
ADASHI, EY .
HUMAN REPRODUCTION, 1994, 9 (05) :815-827
[2]  
ANDERIESZ C, 1995, HUM REPROD, V10, P2377
[3]   LOCALIZATION OF LEUKOCYTE SUBSETS IN THE RAT OVARY DURING THE PERIOVULATORY PERIOD [J].
BRANNSTROM, M ;
MAYRHOFER, G ;
ROBERTSON, SA .
BIOLOGY OF REPRODUCTION, 1993, 48 (02) :277-286
[4]   An age-related ovarian phenotype in mice with targeted disruption of the Cyp 19 (aromatase) gene [J].
Britt, KL ;
Drummond, AE ;
Cox, VA ;
Dyson, M ;
Wreford, NG ;
Jones, MEE ;
Simpson, ER ;
Findlay, JK .
ENDOCRINOLOGY, 2000, 141 (07) :2614-2623
[5]   Postnatal sex reversal of the ovaries in mice lacking estrogen receptors α and β [J].
Couse, JF ;
Hewitt, SC ;
Bunch, DO ;
Sar, M ;
Walker, VR ;
Davis, BJ ;
Korach, KS .
SCIENCE, 1999, 286 (5448) :2328-2331
[6]   Characterization of the hypothalamic-pituitary-gonadal axis in estrogen receptor (ER) null mice reveals hypergonadism and endocrine sex reversal in females lacking ERα but not ERβ [J].
Couse, JF ;
Yates, MM ;
Walker, VR ;
Korach, KS .
MOLECULAR ENDOCRINOLOGY, 2003, 17 (06) :1039-1053
[7]   Prevention of the polycystic ovarian phenotype and characterization of ovulatory capacity in the estrogen receptor-α knockout mouse [J].
Couse, JF ;
Bunch, DO ;
Lindzey, J ;
Schomberg, DW ;
Korach, KS .
ENDOCRINOLOGY, 1999, 140 (12) :5855-5865
[8]   Estrogen receptor null mice: What have we learned and where will they lead us? [J].
Couse, JF ;
Korach, KS .
ENDOCRINE REVIEWS, 1999, 20 (03) :358-417
[9]  
Curtis-Hewitt S, 2003, REPRODUCTION, V125, P143
[10]   The role of estrogen in folliculogenesis [J].
Drummond, AE ;
Findlay, JK .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1999, 151 (1-2) :57-64