Effects of angiotensin II on the acrosome reaction in equine spermatozoa.

K Sabeur, A T Vo, B A Ball
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Abstract

Angiotensin II is a hormone with a wide array of physiological effects that exerts its effect via interaction with two major subtypes of receptor. The results of this study show that angiotensin II (from 1 to 100 nmol l(-1)) initiates acrosomal exocytosis in equine spermatozoa that have undergone capacitation in vitro in a TALP-TEST (Tyrode's albumin lactate pyruvate; 188.7 mmol TES l(-1), 84.8 mmol Tris l(-1)) buffer with cAMP. The acrosome reaction and sperm viability were assessed with fluorescein isothiocyanate-Pisum sativum agglutinin (FITC-PSA) and Hoechst 33258, respectively. The initiation of the acrosome reaction by angiotensin II was strongly inhibited by losartan, a specific angiotensin II type 1 receptor antagonist. Although angiotensin II as well as progesterone both initiated the acrosome reaction in equine spermatozoa, there was no synergistic effect when both agonists were added simultaneously. Initiation of acrosomal exocytosis by angiotensin II was accompanied by a rapid and transient calcium influx that was assessed in capacitated spermatozoa loaded with Fura-2AM. In addition, the angiotensin II-mediated calcium influx was inhibited when spermatozoa were preincubated with losartan. Western blotting with an antibody against angiotensin II type 1 receptor detected a major sperm protein of 60 kDa. Indirect immunofluorescence of non-capacitated spermatozoa with the angiotensin II type 1 receptor antibody revealed labelling in the midpiece and tail. In capacitated spermatozoa, the angiotensin II type 1 receptor was localized mainly over the anterior region of the sperm head, the equatorial segment and occasionally on the postacrosomal region in addition to the sperm tail. In conclusion, this study demonstrated the ability of angiotensin II to stimulate the acrosome reaction in capacitated equine spermatozoa. This effect is mediated via the angiotensin II type 1 receptor and is accompanied by an increase in intracellular calcium.

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血管紧张素II对马精子顶体反应的影响。
血管紧张素II是一种具有广泛生理作用的激素,通过与两种主要受体亚型的相互作用来发挥其作用。本研究结果表明,血管紧张素II(从1到100 nmol l(-1))在体外TALP-TEST (Tyrode's白蛋白乳酸丙酮酸;188.7 mmol TES l(-1), 84.8 mmol Tris l(-1)) cAMP缓冲液。用异硫氰酸荧光素凝集素(FITC-PSA)和Hoechst 33258分别评价顶体反应和精子活力。血管紧张素II的顶体反应被氯沙坦(一种特异性血管紧张素II 1型受体拮抗剂)强烈抑制。虽然血管紧张素II和黄体酮都能引起马精子顶体反应,但同时加入这两种激动剂时没有协同作用。在装载Fura-2AM的有能力精子中,血管紧张素II引发顶体胞外分泌伴随着快速和短暂的钙内流。此外,当精子与氯沙坦预孵育时,血管紧张素ii介导的钙内流被抑制。抗血管紧张素II型1受体抗体的Western blotting检测到60 kDa的主要精子蛋白。血管紧张素II型1受体抗体的间接免疫荧光显示在中间和尾部有标记。在能态精子中,血管紧张素II型1受体主要位于精子头部前部和赤道段,除了精子尾部外,偶尔也位于顶体后区域。总之,本研究证明了血管紧张素II能够刺激马精子顶体反应。这种作用是通过血管紧张素II型1受体介导的,并伴随着细胞内钙的增加。
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