He C L, Damiani P, Ducibella T, Takahashi M, Tanzawa K, Parys J B, Fissore R A
Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts 01003, USA.
Biol Reprod. 1999 Oct;61(4):935-43. doi: 10.1095/biolreprod61.4.935.
Mammalian fertilization is characterized by the presence of long-lasting intracellular calcium ([Ca2+]i) oscillations that are required to induce oocyte activation. One of the Ca2+ channels that may mediate this Ca2+ release is the inositol 1,4, 5-trisphosphate receptor (IP(3)R). Three isoforms of the receptor have been described, but their expression in oocytes and possible roles in mammalian fertilization are not well known. Using isoform-specific antibodies against IP(3)R types 1, 2, and 3 and Western analysis, we determined the isoforms that are expressed in bovine metaphase II oocytes and ovaries. In oocytes, all isoforms are expressed, but type 1 is present in overwhelmingly larger amounts and is likely responsible for the majority of Ca2+ release at fertilization. In ovarian microsomes, all three isoforms appear well expressed, suggesting the participation of all IP(3)R isoforms in ovarian Ca2+ signaling. We then investigated whether the reported cessation/reduction in amplitude of fertilization-associated [Ca2+]i oscillations, which is observed as pronuclear formation approaches, corresponded with down-regulation of the IP(3)R-1 isoform. Fertilization resulted in approximately 40% reduction in the amount of receptor by 16 h postinsemination. In addition, injection of adenophostin A, a potent IP(3)R agonist that elicits high-frequency [Ca2+]i oscillations in mammalian oocytes, induced similar reduction in receptor numbers. Together, these data show that 1) the three IP(3)R isoforms are expressed in bovine oocytes; 2) IP(3)R-1 is likely to mediate most of the Ca2+ release during fertilization; 3) its down-regulation may explain the decline in amplitude of sperm-induced [Ca2+]i rises as fertilization progresses toward pronuclear formation; and 4) agonists of the IP(3)R induce down-regulation of the type-1 receptor in oocytes similar to that evoked by fertilization.
哺乳动物受精的特征是存在持久的细胞内钙([Ca2+]i)振荡,这是诱导卵母细胞激活所必需的。可能介导这种钙释放的钙通道之一是肌醇1,4,5-三磷酸受体(IP(3)R)。已经描述了该受体的三种亚型,但其在卵母细胞中的表达以及在哺乳动物受精中的可能作用尚不清楚。使用针对1型、2型和3型IP(3)R的亚型特异性抗体以及蛋白质印迹分析,我们确定了在牛中期II卵母细胞和卵巢中表达的亚型。在卵母细胞中,所有亚型均有表达,但1型的含量极高,可能是受精时大部分钙释放的原因。在卵巢微粒体中,所有三种亚型似乎都表达良好,表明所有IP(3)R亚型都参与卵巢钙信号传导。然后,我们研究了随着原核形成临近,受精相关的[Ca2+]i振荡幅度的报道的停止/降低是否与IP(3)R-1亚型的下调相对应。受精导致授精后16小时受体数量减少约40%。此外,注射腺嘌呤磷酯A(一种在哺乳动物卵母细胞中引发高频[Ca2+]i振荡的强效IP(3)R激动剂)会导致受体数量出现类似的减少。总之,这些数据表明:1)三种IP(3)R亚型在牛卵母细胞中表达;2)IP(3)R-1可能在受精过程中介导大部分钙释放;3)其下调可能解释了随着受精向原核形成发展,精子诱导的[Ca2+]i升高幅度的下降;4)IP(3)R激动剂在卵母细胞中诱导1型受体下调,类似于受精所引发的下调。