Continuous loss of oocytes throughout meiotic prophase in the normal mouse ovary

被引:104
|
作者
McClellan, KA
Gosden, R
Taketo, T
机构
[1] McGill Univ, Dept Biol, Montreal, PQ H3A 1B1, Canada
[2] McGill Univ, Dept Obs Gyn, Montreal, PQ H3A 1A1, Canada
[3] McGill Univ, Urol Res Lab, Dept Surg, Montreal, PQ H3A 1A1, Canada
关键词
mouse fetal ovary; germ cell; oocyte; GCNA-1; MVH; meiotic prophase;
D O I
10.1016/S0012-1606(03)00132-5
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The number of germ cells reaches the maximum just prior to entry into meiosis, yet decreases dramatically by a few days after birth in the female mouse, rat, and human. Previous studies have reported a major loss at the pachytene stage of meiotic prophase during fetal development, leading to the hypothesis that chromosomal pairing abnormalities may be a signal for oocyte death. However, the identification as well as the quantification of germ cells in these studies have been questioned. A recent study using Mouse Vasa Homologue (MVH) as a germ cell marker reached a contradictory conclusion claiming that oocyte loss occurs in the mouse only after birth. In the present study, we established a new method to quantify murine germ cells by using Germ Cell Nuclear Antigen-1 (GCNA-1) as a germ cell marker. Comparison of GCNA-1 and MVH immunolabeling revealed that the two markers identify the same population of germ cells. However, nuclear labeling of GCNA-1 was better suited for counting germ cells in histological sections as well as for double labeling with the antibody against synaptonemal complex (SC) proteins in chromosome spreading preparations. The latter experiment demonstrated that the majority of GCNA-1-labeled cells entered and progressed through meiotic prophase during fetal development. The number of GCNA-1-positive cells in the ovary was estimated by counting the labeled cells retained in chromosome spreading preparations and also in histological sections by using the ratio estimation method. Both methods demonstrated a continuous decline in the number of GCNA-1-labeled cells during fetal development when the oocytes progress through meiotic prophase. These observations suggest that multiple causes are responsible for oocyte elimination. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:334 / 348
页数:15
相关论文
共 50 条
  • [1] MEIOTIC PROGRESSION OF MOUSE OOCYTES THROUGHOUT FOLLICLE GROWTH AND OVULATION IN-VITRO
    HARTSHORNE, GM
    SARGENT, IL
    BARLOW, DH
    HUMAN REPRODUCTION, 1994, 9 (02) : 352 - 359
  • [2] Caspase 9 is constitutively activated in mouse oocytes and plays a key role in oocyte elimination during meiotic prophase progression
    Ene, Adriana C.
    Park, Stephanie
    Edelmann, Winfried
    Taketo, Teruko
    DEVELOPMENTAL BIOLOGY, 2013, 377 (01) : 213 - 223
  • [3] Regulation of the meiotic prophase I to metaphase I transition in mouse spermatocytes
    Fengyun Sun
    Mary Ann Handel
    Chromosoma, 2008, 117 : 471 - 485
  • [4] An RNAi screen to identify proteins required for cohesion rejuvenation during meiotic prophase in Drosophila oocytes
    Haseeb, Muhammad A.
    Bernys, Alana C.
    Dickert, Erin E.
    Bickel, Sharon E.
    G3-GENES GENOMES GENETICS, 2024, 14 (08):
  • [5] The regulation of maturation promoting factor during prophase I arrest and meiotic entry in mammalian oocytes
    Adhikari, Deepak
    Liu, Kui
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2014, 382 (01) : 480 - 487
  • [6] Molecular analysis of the effects of steroid hormones on mouse meiotic prophase I progression
    Burks, Deion M.
    McCoy, Margaret R.
    Dutta, Sudipta
    Mark-Kappeler, Connie J.
    Hoyer, Patricia B.
    Pepling, Melissa E.
    REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2019, 17 (01)
  • [7] Induction of meiotic maturation in mouse oocytes by adenosine analogs
    Downs, Stephen M.
    Chen, Jing
    MOLECULAR REPRODUCTION AND DEVELOPMENT, 2006, 73 (09) : 1159 - 1168
  • [8] Molecular analysis of the effects of steroid hormones on mouse meiotic prophase I progression
    Deion M. Burks
    Margaret R. McCoy
    Sudipta Dutta
    Connie J. Mark-Kappeler
    Patricia B. Hoyer
    Melissa E. Pepling
    Reproductive Biology and Endocrinology, 17
  • [9] α-endosulfine (ENSA) regulates exit from prophase I arrest in mouse oocytes
    Matthews, Lauren M.
    Evans, Janice P.
    CELL CYCLE, 2014, 13 (10) : 1639 - 1649
  • [10] Exposure of mouse oocytes to bisphenol A causes meiotic arrest but not aneuploidy
    Eichenlaub-Ritter, Ursula
    Vogt, Edgar
    Cukurcam, Suna
    Sun, Fengyun
    Pacchierotti, Francesca
    Parry, Jim
    MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2008, 651 (1-2) : 82 - 92