INIAV, Instituto Nacional de Investigação Agrária e Veterinária, Unidade de Biotecnologias e Recursos Genéticos - Santarém, Quinta da Fonte Boa, 2000-048 Vale de Santarém, Santarém, Portugal.
CIISA, Faculdade de Medicina Veterinária, Universidade de Lisboa, Av. da Universidade Técnica, 1300-477, Lisbon, Portugal.
Purinergic Signal. 2020 Mar;16(1):85-96. doi: 10.1007/s11302-020-09690-6. Epub 2020 Feb 10.
The improvement of cryopreserved oocyte survival is imperative for the preservation of female fertility. In this study, we investigate whether P2Y2 receptors (P2Y2R) can be directly implicated in calcium (Ca) homeostasis misbalances observed during the cryopreservation process of cumulus oocyte complexes (COC). Firstly, RNA was extracted from bovine immature and mature oocytes and cumulus cells and real-time PCR performed to identify P2Y2R transcripts (experiment 1). Changes in intracellular calcium concentration [Ca2+]i of mature COC and oocytes (experiment 2) were measured upon exposure to cryoprotectants (CPA), UTP (P2Y2R stimulator, 100 μM), and/or suramin (P2Y2R inhibitor, 100 and 300 μM). The functional role of P2Y2R was investigated by analyzing the effect on oocyte viability of its modulation prior and during oocyte exposure to CPA (experiment 3). Mature COC were randomly divided into groups, and exposed to CPA and different P2Y2 modulators. Oocytes' viability, cortical granules location, and competence for development were assessed. Results showed that P2Y2R mRNAs are expressed in both oocytes and cumulus cells. Stimulation with UTP and CPA led to [Ca2+]i increase, and this effect was totally or partially blocked by suramin (P2Y2R inhibitor). Oocyte exposure to CPA and UTP reduced embryo rates compared with control and suramin100μM (P ≤ 0.04). The observed enhanced premature zona hardening in oocytes exposed to CPA (P = 0.04) and UTP (P = 0.005) stimulus was inhibited by suramin 100 μM. In conclusion, inhibition of P2Y2R during cryoprotectant exposure reduces premature intracellular Ca release and significantly improves the developmental competence of exposed bovine oocytes.
提高冷冻保存卵母细胞的存活率对于保存女性生育能力至关重要。在这项研究中,我们研究了 P2Y2 受体 (P2Y2R) 是否可以直接涉及到卵丘卵母细胞复合物 (COC) 冷冻保存过程中观察到的钙 (Ca) 稳态失衡。首先,从牛未成熟和成熟卵母细胞和卵丘细胞中提取 RNA,并进行实时 PCR 以鉴定 P2Y2R 转录本(实验 1)。暴露于冷冻保护剂 (CPA)、UTP(P2Y2R 激动剂,100 μM)和/或苏拉明(P2Y2R 抑制剂,100 和 300 μM)后,测量成熟 COC 和卵母细胞的细胞内钙离子浓度 [Ca2+]i(实验 2)。通过分析其在卵母细胞暴露于 CPA 之前和期间对卵母细胞活力的影响,研究了 P2Y2R 的功能作用(实验 3)。将成熟的 COC 随机分为几组,暴露于 CPA 和不同的 P2Y2 调节剂中。评估卵母细胞的活力、皮质颗粒位置和发育能力。结果表明,P2Y2R mRNA 在卵母细胞和卵丘细胞中均有表达。UTP 和 CPA 的刺激导致 [Ca2+]i 增加,苏拉明(P2Y2R 抑制剂)完全或部分阻断了这种作用。与对照组和苏拉明 100μM 相比,卵母细胞暴露于 CPA 和 UTP 导致胚胎率降低(P≤0.04)。CPA(P=0.04)和 UTP(P=0.005)刺激下观察到的卵母细胞过早的透明带硬化增强被苏拉明 100μM 抑制。总之,在暴露于冷冻保护剂期间抑制 P2Y2R 可减少过早的细胞内 Ca 释放,并显著提高暴露的牛卵母细胞的发育能力。