Pons-Rejraji H, Artonne C, Sion B, Brugnon F, Canis M, Janny L, Grizard G
Laboratoire de Biologie du Développement et de la Reproduction, Clermont Université, Université d'Auvergne, Fertilité humaine environnement séminal péritonéal et spermatozoïdes, Clermont-Ferrand, France.
Int J Androl. 2011 Dec;34(6 Pt 1):568-80. doi: 10.1111/j.1365-2605.2010.01116.x. Epub 2010 Oct 1.
Seminal fluid inhibits sperm capacitation mainly because of its high cholesterol content. Prostasomes are the main source of cholesterol in seminal fluid. They are known to have numerous protective properties and are able to transfer proteins and lipids to spermatozoa, but their impact on capacitation and acrosome reaction (AR) is not yet well understood. The aim of this study was to determine the effects of prostasomes on human sperm capacitation and AR. After 80% Percoll selection, freshly ejaculated human spermatozoa were incubated for 3 h under capacitating conditions with prostasomes, phosphodiesterase inhibitor 3-iso-butyl-methylxantine (IBMX), or a combination of prostasomes and IBMX. Physiological concentration of prostasomes significantly decreased tyrosine phosphorylation levels of human sperm capacitation markers P110 and P80 (p < 0.01), and the proportions of capacitated (p < 0.05) and acrosome-reacted spermatozoa (p < 0.05). Prostasomes significantly increased the proportion of spermatozoa that did not incorporate propidium iodide and significantly attenuated the effect of IBMX on P110 tyrosine phosphorylation. Prostasomes had no effect on the pH(i) increase associated with capacitation. They significantly increased intracellular cAMP concentration (cAMP) and, when prostasomes and IBMX were present together, cAMP was further increased. To our knowledge, this is the first study to show clearly that prostasomes inhibit capacitation and spontaneous AR.
精液主要因其高胆固醇含量而抑制精子获能。前列腺小体是精液中胆固醇的主要来源。已知它们具有多种保护特性,并且能够将蛋白质和脂质转移到精子上,但其对获能和顶体反应(AR)的影响尚未得到充分了解。本研究的目的是确定前列腺小体对人类精子获能和AR的影响。经过80% Percoll筛选后,将新鲜射出的人类精子在获能条件下与前列腺小体、磷酸二酯酶抑制剂3-异丁基-甲基黄嘌呤(IBMX)或前列腺小体与IBMX的组合一起孵育3小时。生理浓度的前列腺小体显著降低了人类精子获能标志物P110和P80的酪氨酸磷酸化水平(p < 0.01),以及获能精子(p < 0.05)和顶体反应精子的比例(p < 0.05)。前列腺小体显著增加了未掺入碘化丙啶的精子比例,并显著减弱了IBMX对P110酪氨酸磷酸化的作用。前列腺小体对与获能相关的细胞内pH(i)升高没有影响。它们显著增加了细胞内cAMP浓度([cAMP](i)),并且当同时存在前列腺小体和IBMX时,[cAMP](i)进一步升高。据我们所知,这是第一项清楚表明前列腺小体抑制获能和自发AR的研究。