Atresia revisited: two basic patterns of atresia of bovine antral follicles

被引:93
作者
Irving-Rodgers, HF [1 ]
van Wezel, IL
Mussard, ML
Kinder, JE
Rodgers, RJ
机构
[1] Flinders Univ S Australia, Dept Med, Bedford Pk, SA 5042, Australia
[2] Univ Nebraska, Dept Anim Sci, Lincoln, NE 68583 USA
关键词
D O I
10.1530/rep.0.1220761
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Our observations of bovine follicles indicated that the original histological classifications of atresia were inaccurate. A detailed histological, ultrastructural and immunohistochemical study of antral follicles from bovine ovaries collected from an abattoir and from animals whose large follicles had been monitored by ultrasonography was conducted to investigate this further. Nidogen and CD68 were immunolocalized to observe the follicular basal lamina and macrophages, respectively. In randomly collected ovaries, approximately one quarter of all antral follicles were undergoing antral atresia, as designated in this study. Antral atresia was characterized by early destruction of the layers of the membrana granulosa closest to the antrum, whereas the most basal cells remained intact. Numerous pyknotic nuclei were observed in the most antral layers and in the antrum close to the membrana granulosa. This is the classic description of atretic follicles and was observed at all sizes of follicle development and almost universally in large follicles (> 5 mm in diameter), including dominant follicles. Basal atretic follicles, as designated in this study, were almost as prevalent as the antral atretic follicles, and were characterized by initial destruction of the most basal layer of granulosa cells, whereas the cells in the most antral layers remained associated with each other and were predominantly healthy. Pyknotic nuclei and the nuclei of dying basal cells budded into apoptotic bodies were observed rarely. The basal lamina of basal atretic follicles was often breached by macrophages, which were phagocytosing dying basal granulosa cells. The theca was characterized by an increased deposition of collagen, and the cells were orientated randomly, rather than lying parallel to the membrana granulosa as in healthy follicles. Basal atresia occurred in small (< 5 mm in diameter) follicles only. Importantly, these basal atretic follicles were originally identified incorrectly in the literature. Thus, on the basis of the results of this study and another on the expression of steroidogenic enzymes in atretic follicles, it is suggested that the standard biochemical methods for measuring steroid hormone concentrations in follicular fluids to assess atresia should be re-evaluated.
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页码:761 / 775
页数:15
相关论文
共 27 条
[1]  
[Anonymous], [No title captured]
[2]  
Asselin E, 2000, BIOL SIGNAL RECEPT, V9, P87
[3]   Analysis of atresia in bovine follicles using different methods: Flow cytometry, enzyme-linked immunosorbent assay, and classic histology [J].
Blondin, P ;
Dufour, M ;
Sirard, MA .
BIOLOGY OF REPRODUCTION, 1996, 54 (03) :631-637
[4]   DOES APOPTOSIS OCCUR DURING FOLLICULAR ATRESIA IN THE FOLLICULAR WALLS OF THE PORCINE OVARY [J].
DERECKA, K ;
KALAMARZ, H ;
ZIECIK, AJ .
REPRODUCTION IN DOMESTIC ANIMALS, 1995, 30 (01) :32-35
[5]   IDENTIFICATION AND INTERACTION REPERTOIRE OF LARGE FORMS OF THE BASEMENT-MEMBRANE PROTEIN NIDOGEN [J].
DZIADEK, M ;
PAULSSON, M ;
TIMPL, R .
EMBO JOURNAL, 1985, 4 (10) :2513-2518
[6]   OVARIAN FOLLICULAR-GROWTH AND DEVELOPMENT IN MAMMALS [J].
FORTUNE, JE .
BIOLOGY OF REPRODUCTION, 1994, 50 (02) :225-232
[7]   Selection of the dominant follicle in cattle [J].
Ginther, OJ ;
Wiltbank, MC ;
Fricke, PM ;
Gibbons, JR ;
Kot, K .
BIOLOGY OF REPRODUCTION, 1996, 55 (06) :1187-1194
[8]  
Greenwald G.S., 1988, P387
[9]   A COMPARISON OF HISTOLOGICAL AND NON-HISTOLOGICAL INDEXES OF ATRESIA AND FOLLICULAR FUNCTION [J].
GRIMES, RW ;
MATTON, P ;
IRELAND, JJ .
BIOLOGY OF REPRODUCTION, 1987, 37 (01) :82-88
[10]   The detection of CD2+, CD4+, CD8+, and WC1+T lymphocytes, B cells and macrophages in fixed and paraffin embedded bovine tissue using a range of antigen recovery and signal amplification techniques [J].
Gutierrez, M ;
Forster, FI ;
McConnell, SA ;
Cassidy, JP ;
Pollock, JM ;
Bryson, DG .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1999, 71 (3-4) :321-334