Stockpiling of transitional and classic primary follicles in ovaries of women with polycystic ovary syndrome

被引:191
作者
Maciel, GAR
Baracat, EC
Benda, JA
Markham, SM
Hensinger, K
Chang, RJ
Erickson, GF [1 ]
机构
[1] Univ Calif San Diego, Dept Reprod Med, La Jolla, CA 92093 USA
[2] Univ Fed Sao Paulo, BR-01311940 Sao Paulo, Brazil
[3] Univ Iowa, Carver Coll Med, Iowa City, IA 52242 USA
关键词
D O I
10.1210/jc.2004-0643
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recently, we proposed an oocyte-growth differentiation factor-9 hypothesis that predicts alterations in the initial stages of folliculogenesis in polycystic ovary syndrome (PCOS) ovaries. Here, we test this hypothesis by scoring the composition of follicles in normal and PCOS ovaries. Follicles were classified as primordial, transitional primary, classic primary, secondary, and Graafian. A total of 2274 follicles were scored. The total number of growing follicles was significantly greater in PCOS ovaries than normal, but the number of nongrowing primordial follicles did not differ. Consequently, the increase in growing follicles in PCOS cannot be explained by increased primordial follicle recruitment. Differential counts showed that the number of growing follicles at each stage of development was significantly greater: PCOS had 2.7-fold more primary, 1.8-fold more secondary, and 2-fold more Graafian follicles than normal. The greatest effect was on the classic primary follicles where the number was almost 5-fold greater in PCOS ovaries. The absence of apoptosis in normal and PCOS preantral follicles argues that the increase in growing follicles in PCOS cannot be explained by changes in atresia. We conclude, therefore, that primary follicle growth is abnormally slow in PCOS and the dynamics are reflected in a stockpiling of classic primary follicles.
引用
收藏
页码:5321 / 5327
页数:7
相关论文
共 66 条
[1]   Human growth differentiation factor 9 (GDF-9) and its novel homolog GDF-9B are expressed in oocytes during early folliculogenesis [J].
Aaltonen, J ;
Laitinen, MP ;
Vuojolainen, K ;
Jaatinen, R ;
Horelli-Kuitunen, N ;
Seppä, L ;
Louhio, H ;
Tuuri, T ;
Sjöberg, J ;
Bützow, R ;
Hovatta, O ;
Dale, L ;
Ritvos, O .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (08) :2744-2750
[2]  
[Anonymous], 1992, POLYCYSTIC OVARY SYN
[3]   Characterization of oocyte and follicle development in growth differentiation factor-9-deficient mice [J].
Carabatsos, MJ ;
Elvin, J ;
Matzuk, MM ;
Albertini, DF .
DEVELOPMENTAL BIOLOGY, 1998, 204 (02) :373-384
[4]   EVIDENCE FOR THE PRESENCE OF A MAJOR GENE INFLUENCING OVULATION RATE ON THE X-CHROMOSOME OF SHEEP [J].
DAVIS, GH ;
MCEWAN, JC ;
FENNESSY, PF ;
DODDS, KG ;
FARQUHAR, PA .
BIOLOGY OF REPRODUCTION, 1991, 44 (04) :620-624
[5]  
Dong LW, 1996, J MOL RECOGNIT, V9, P383, DOI 10.1002/(SICI)1099-1352(199634/12)9:5/6<383::AID-JMR269>3.0.CO
[6]  
2-Z
[7]   Insulin resistance and the polycystic ovary syndrome: Mechanism and implications for pathogenesis [J].
Dunaif, A .
ENDOCRINE REVIEWS, 1997, 18 (06) :774-800
[8]   Paracrine actions of growth differentiation factor-9 in the mammalian ovary [J].
Elvin, JA ;
Clark, AT ;
Wang, P ;
Wolfman, NM ;
Matzuk, MM .
MOLECULAR ENDOCRINOLOGY, 1999, 13 (06) :1035-1048
[9]   Molecular characterization of the follicle defects in the growth differentiation factor 9-deficient ovary [J].
Elvin, JA ;
Yan, CN ;
Wang, P ;
Nishimori, K ;
Matzuk, MM .
MOLECULAR ENDOCRINOLOGY, 1999, 13 (06) :1018-1034
[10]  
Erickson GE, 1993, OVARY, P561