Chongqing Key Laboratory of Human Embryo Engineering, Center for Reproductive Medicine, Women and Children's Hospital of Chongqing Medical University, Chongqing 400012, China.
Chongqing Clinical Research Center for Reproductive Medicine, Center for Reproductive Medicine, Chongqing Health Center for Women and Children, Chongqing 400012, China.
Asian J Androl. 2024 Jul 1;26(4):389-395. doi: 10.4103/aja202376. Epub 2024 Mar 5.
Failure of oocyte activation, including polyspermy and defects in pronuclear (PN) formation, triggers early embryonic developmental arrest. Many studies have shown that phospholipase C zeta 1 ( PLCZ1 ) mutations cause failure of PN formation following intracytoplasmic sperm injection (ICSI); however, whether PLCZ1 mutation is associated with polyspermy during in vitro fertilization (IVF) remains unknown. Whole-exome sequencing (WES) was performed to identify candidate mutations in couples with primary infertility. Sanger sequencing was used to validate the mutations. Multiple PLCZ1 -mutated sperm were injected into human and mouse oocytes to explore whether PN formation was induced. Assisted oocyte activation (AOA) after ICSI was performed to overcome the failure of oocyte activation. We identified three PLCZ1 mutations in three patients who experienced polyspermy during IVF cycles, including a novel missense mutation c.1154C>T, p.R385Q. PN formation failure was observed during the ICSI cycle. However, injection of multiple PLCZ1- mutated sperm induced PN formation, suggesting that the Ca 2+ oscillations induced by the sperm exceeded the necessary threshold for PN formation. AOA after ICSI enabled normal fertilization, and all patients achieved successful pregnancies. These findings expand the mutational spectrum of PLCZ1 and suggest an important role for PLCZ1 in terms of blocking polyspermy. Furthermore, this study may benefit genetic diagnoses in cases of abnormal fertilization and provide potential appropriate therapeutic measures for these patients with sperm-derived polyspermy.
卵母细胞激活失败,包括多精受精和原核(PN)形成缺陷,会引发早期胚胎发育停滞。许多研究表明,磷脂酶 C ζ 1(PLCZ1)突变会导致卵母细胞胞质内单精子注射(ICSI)后 PN 形成失败;然而,PLCZ1 突变是否与体外受精(IVF)中的多精受精有关尚不清楚。进行全外显子组测序(WES)以鉴定原发性不孕夫妇中的候选突变。Sanger 测序用于验证突变。将多个 PLCZ1 突变精子注入人卵和小鼠卵中,以探讨是否诱导 PN 形成。对 ICSI 后进行辅助卵母细胞激活(AOA)以克服卵母细胞激活失败。我们在三名在 IVF 周期中经历多精受精的患者中发现了三个 PLCZ1 突变,包括一个新的错义突变 c.1154C>T,p.R385Q。在 ICSI 周期中观察到 PN 形成失败。然而,注射多个 PLCZ1 突变精子诱导了 PN 形成,这表明精子诱导的 Ca 2+ 振荡超过了 PN 形成所必需的阈值。ICSI 后的 AOA 实现了正常受精,所有患者均成功妊娠。这些发现扩展了 PLCZ1 的突变谱,并表明 PLCZ1 在阻止多精受精方面具有重要作用。此外,这项研究可能有益于异常受精病例的遗传诊断,并为这些精子源性多精受精患者提供潜在的适当治疗措施。