非洲爪蟾(Xenopus laevis)的受精需要一种源自卵子的PLC来发出快速阻断多精的信号。

microPublication biology Pub Date : 2025-07-30 eCollection Date: 2025-01-01 DOI:10.17912/micropub.biology.001638
Kayla M Komondor, Katherine G Sharp, Anne E Carlson
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引用次数: 0

摘要

非洲爪蟾受精触发钙释放和膜去极化,激活多精快速阻滞。这种去极化需要磷脂酶C (PLC)的活性,但PLC的身份和来源尚不清楚。我们之前报道过,在哺乳动物和鸟类中编码精子来源的PLCζ的PLCZ1在Pipidae青蛙中被删除,这提示了另一种机制。在这里,我们使用不可逆的PLC抑制剂U73122来测试驱动快速块的PLC是来自卵子还是精子。抑制卵子中的PLC活性,而不抑制精子中的PLC活性,消除了受精引起的去极化,导致多精子。这些发现表明,X. laevis依赖于卵源性PLC来发出快速阻滞信号,揭示了受精触发的钙信号通路,这一机制与其他脊椎动物不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fertilization in the African clawed frog <i>, Xenopus laevis</i> , requires an egg-derived PLC to signal the fast block to polyspermy.

Fertilization in the African clawed frog , Xenopus laevis , requires an egg-derived PLC to signal the fast block to polyspermy.

Fertilization in Xenopus laevis triggers calcium release and membrane depolarization to activate the fast block to polyspermy. This depolarization requires phospholipase C (PLC) activity, but the identity and origin of the PLC remained unclear. We previously reported that PLCZ1 , which encodes the sperm-derived PLCζ used in mammals and birds, was deleted in Pipidae frogs, suggesting an alternative mechanism. Here, we used the irreversible PLC inhibitor U73122 to test whether the PLC driving the fast block originates from the egg or sperm. Inhibiting PLC activity in the egg, but not in the sperm, abolished the fertilization-evoked depolarization and led to polyspermy. These findings demonstrate that X. laevis relies on an egg-derived PLC to signal the fast block, revealing a fertilization-triggered calcium signaling pathway that is mechanistically distinct from other vertebrates.

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