New insights into the pathogenesis of cystic follicles in cattle: Microarray analysis of gene expression in granulosa cells

被引:37
作者
Grado-Ahuir, J. A. [1 ]
Aad, P. Y. [1 ]
Spicer, L. J. [1 ]
机构
[1] Oklahoma State Univ, Dept Anim Sci, Stillwater, OK 74078 USA
关键词
cattle; cystic follicle; gene expression; granulosa cell; microarray analysis; OVARIAN FOLLICULAR CYSTS; GROWTH-FACTOR-I; HUMAN CHORIONIC-GONADOTROPIN; MESSENGER-RIBONUCLEIC-ACID; FRIZZLED-RELATED PROTEIN-4; APOPTOSIS-ASSOCIATED GENE; FACTOR BINDING-PROTEINS; LARGE ANTRAL FOLLICLES; NECROSIS-FACTOR-ALPHA; BOVINE GRANULOSA;
D O I
10.2527/jas.2010-3463
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Ovarian follicular growth and development are regulated by extraovarian and intraovarian factors, which influence granulosa cell proliferation and differentiation. However, the molecular mechanisms that drive follicular growth are not completely understood. Ovarian follicular cysts are one of the most common causes of reproductive failure in dairy cattle. Nevertheless, the primary cause of cyst formation has not been clearly established. A gene expression comparison may aid in elucidating the causes of ovarian cyst disease. Our objective was to identify differentially expressed genes in ovarian granulosa cells between normal dominant and cystic follicles of cattle. Granulosa cells and follicular fluid were isolated from dominant and cystic follicles collected via either ultrasound-guided aspiration from dairy cows (n = 24) or slaughterhouse ovaries from beef cows (n = 23). Hormonal analysis for progesterone, estradiol, and androstenedione in follicular fluid was performed by RIA. Total RNA was extracted and hybridized to 6 Affymetrix GeneChip Bovine Genome Arrays (Affymetrix, Santa Clara, CA). Abundance of mRNA for differentially expressed selected genes was determined through quantitative realtime reverse-transcription PCR. Follicular cysts showed greater (P < 0.05) progesterone, lesser (P < 0.05) estradiol, and no differences (P > 0.10) in androstenedione concentrations compared with noncystic follicles. A total of 163 gene sequences were differentially expressed (P < 0.01), with 19 upregulated and 144 downregulated. From selected target genes, quantitative real-time reverse-transcription PCR confirmed angiogenin, PGE(2) receptor 4, and G-protein coupled receptor 34 genes as upregulated in cystic follicles, and Indian hedgehog protein precursor and secreted frizzled-related protein 4 genes as downregulated in cystic follicles. Further research is required to elucidate the role of these factors in follicular development and cyst formation.
引用
收藏
页码:1769 / 1786
页数:18
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