首页> 外文期刊>The Journal of Reproduction and Development >Relative Changes in mRNA Expression of Angiopoietins and Receptors Tie in Bovine Corpus Luteum during Estrous Cycle and Prostaglandin F_(2α)-induced Luteolysis: A Possible Mechanism for the Initiation of Luteal Regression
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Relative Changes in mRNA Expression of Angiopoietins and Receptors Tie in Bovine Corpus Luteum during Estrous Cycle and Prostaglandin F_(2α)-induced Luteolysis: A Possible Mechanism for the Initiation of Luteal Regression

机译:牛黄体发情周期和前列腺素F_(2α)诱导的黄体溶解过程中血管生成素及其受体领带的mRNA表达的相对变化:黄体退化的一种可能机制

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Local angiogenesis and angiolysis in the corpus luteum (CL) relate to the luteal function, Recent studies indicate that angiopoietins (ANPT) and their receptors Tie regulate remodeling of microvasculature. We therefore examined 1) the relative changesin the expression of mRNA for ANPT-1, ANPT-2, Tiel and Tie2 in bovine CL by semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) during the estrous cycle and prostaglandin F_(2α) (PGF_(2α))-induced luteolysis, and 2) the effect of ANPT-2 on progesterone (P4) release from CL at the late stage of the estrous cycle by an in vitro microdialysis system (MDS). The CLs were classified into 4 stages (early: Day 2-5, n=7, mid: Day 8-12, n=15, late: Day 15-17, n=9, regressing: Day >18, n=19). The levels of ANPT-1 mRNA in early and regressing CL were lower than those in mid and late CL, whereas ANPT-2 mRNA expression did not change during the estrous cycle. The Tie2 mRNA expression decreased as the CL aged. During PGF_(2α)-induced luteolysis, ANPT-2 mRNA expression was acutely and temporally increased at 2 h after PGF_(2α) injection. The expression of ANPT-1 mRNA was decreased from 4 h after PGF_(2α) injection and kept low levels. In the experiment with the in vitro MDS, an infusion of ANPT-2 (100 ng/ml) acutely inhibited P4 release from late CL Overall, results suggest that decrease of ANPT-1 mRNA is a basic mechanism of vascular remodeling in CL. In addition, ANPT-2 might play a role in regulation of P4 secretion in CL during luteolysis.
机译:黄体(CL)中的局部血管生成和血管溶解与黄体功能有关。最近的研究表明,血管生成素(ANPT)及其受体Tie调节微血管的重塑。因此,我们检查了1)在发情周期和前列腺素F_期间,通过半定量逆转录聚合酶链反应(RT-PCR)对牛CL中ANPT-1,ANTT-2,Tiel和Tie2 mRNA表达的相对变化。 2α)(PGF_(2α))诱导的黄体溶解,以及2)在体外动透系统(MDS)的发情周期后期,ANTP-2对黄体酮从CL释放的影响。 CL分为4个阶段(早期:第2-5天,n = 7,中期:第8-12天,n = 15,晚期:第15-17天,n = 9,回归:第18天以上,n = 19 )。早期和复发性CL的ANPT-1 mRNA水平低于中晚期CL,而在动情周期中ANPT-2 mRNA的表达没有变化。随着年龄的增长,Tie2 mRNA的表达下降。在PGF_(2α)引起的黄体溶解过程中,注射PGF_(2α)后2 h ANPT-2 mRNA的表达迅速而短暂地增加。 PGF_(2α)注射后4 h ANPT-1 mRNA表达下降,并保持较低水平。在体外MDS实验中,输注ANPT-2(100 ng / ml)急性抑制了CL晚期的P4释放。结果表明,ANPT-1 mRNA的降低是CL中血管重塑的基本机制。此外,ANTPT-2可能在黄体溶解过程中调节CL中P4的分泌。

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