Expression of estrogen and progesterone receptors in the bovine ovary during estrous cycle and pregnancy

被引:82
作者
Berisha, B [1 ]
Pfaffl, MW [1 ]
Schams, D [1 ]
机构
[1] Tech Univ Munich, Inst Physiol, D-85350 Freising Weihenstephan, Germany
关键词
bovine ovary; steroid; receptor; expression;
D O I
10.1385/ENDO:17:3:207
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The objective of the study was to demonstrate the mRNA expression of estrogen receptor alpha (ERalpha), ERP, and progesterone receptor (PR) by block reverse transcription-polymerase chain reaction (RT-PCR) and real-time RT-PCR (LightCycler) in bovine ovarian follicles and in corpus luteum during the estrous cycle and pregnancy. The mRNA expression of ERalpha and ERP mRNA in theca interna tissue (TI) (lower pg/mug RNA) increased continuously and significantly during final growth of follicles, with much higher levels for ERalpha. The mRNA expression of ERalpha and ERP in granulosa cells (GC) (fg/mug RNA) increased continuously during follicle growth but without any significant change. The expression of mRNA for PR in follicles (lower fg/mug RNA) increased continuously to maximum level in preovulatory follicles with a significant change only in TI. The highest mRNA expression for ERalpha (fg/mug RNA) was detected in corpus luteum (CL) during the early luteal phase, following by a significant decrease of expression during the mid, late, and regression phases. In contrast, ERP mRNA expression is relatively high during the early stage, decreased during the late early and mid luteal phase, and increased significantly again during the late luteal phase and after CL regression. During pregnancy (>3 mo), low levels of ERalpha and ERP mRNA expression (<25 fg/mug RNA) with no significant changes were measured. No significant change in PR mRNA expression (levels <13 fg/mug RNA) during the estrous cycle and pregnancy in bovine CL were found. The results suggest an autocrine/paracrine role of steroid receptors in the regulation of final follicle growth and corpus luteum formation and function.
引用
收藏
页码:207 / 214
页数:8
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