Laboratory of Cell and Developmental Biology, Graduate School of Bioscience, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.
Laboratory of Cell and Developmental Biology, Graduate School of Bioscience, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama 226-8501, Japan; Research Center for Marine Biology, Graduate School of Life Sciences, Tohoku University, Asamushi, Aomori 039-3501, Japan.
Dev Biol. 2014 Aug 1;392(1):80-92. doi: 10.1016/j.ydbio.2014.04.020. Epub 2014 May 6.
Jellyfish eggs neither undergo apparent cortical reaction nor show any significant change in the membrane potential at fertilization, but nevertheless show monospermy. Utilizing the perfectly transparent eggs of the hydrozoan jellyfish Cytaeis uchidae, here we show that the polyspermy block is accomplished via a novel mechanism: a collaboration between Ca(2+) and mitogen-activated protein kinase (MAPK). In Cytaeis, adhesion of a sperm to the animal pole surface of an egg was immediately followed by sperm-egg fusion and initiation of an intracellular Ca(2+) rise from this site. The elevated Ca(2+) levels lasted for several minutes following the sperm-egg fusion. The Ca(2+) rise proved to be necessary and sufficient for a polyspermy block, as inhibiting a Ca(2+) rise with EGTA promoted polyspermy, and conversely, triggering a Ca(2+) rise by inositol 1,4,5-trisphosphate (IP3) or excess K(+) immediately abolished the egg's capacity for sperm-egg fusion. A Ca(2+) rise at fertilization or by artificial stimulations evoked dephosphorylation of MAPK in eggs. The eggs in which phosphorylated MAPK was maintained by injection of mRNA for MAPK kinase kinase (Mos), like intact eggs, exhibited a Ca(2+) rise at fertilization or by IP3 injection, and shut down the subsequent sperm-egg fusion. However, the Mos-expressing eggs became capable of accepting sperm following the arrest of Ca(2+) rise. In contrast, addition of inhibitors of MAPK kinase (MEK) to unfertilized eggs caused MAPK dephosphorylation without elevating Ca(2+) levels, and prevented sperm-egg fusion. Rephosphorylation of MAPK by injecting Mos mRNA after fertilization recovered sperm attraction, which is known to be another MAPK-dependent event, but did not permit subsequent sperm-egg fusion. Thus, it is possible that MAPK dephosphorylation irreversibly blocks sperm-egg fusion and reversibly suppresses sperm attraction. Collectively, our data suggest that both the fast and late mechanisms dependent on Ca(2+) and MAPK, respectively, ensure a polyspermy block in jellyfish eggs.
水母卵在受精时既没有明显的皮层反应,也没有膜电位的显著变化,但仍然表现出单精入卵。利用水螅水母 Cytaeis uchidae 的完全透明卵,我们在这里表明,多精入卵的阻断是通过一种新的机制实现的:钙离子和丝裂原活化蛋白激酶(MAPK)的协同作用。在 Cytaeis 中,精子与卵的动物极表面的黏附紧接着是精子-卵融合,并从此处开始细胞内钙离子的上升。钙离子的上升在精子-卵融合后持续了几分钟。钙离子的上升被证明是多精入卵阻断所必需和充分的,因为用 EGTA 抑制钙离子的上升促进了多精入卵,反之,用三磷酸肌醇(IP3)或过量钾离子触发钙离子的上升立即消除了卵的精子-卵融合能力。受精时或人工刺激引起的钙离子上升会导致卵中 MAPK 的去磷酸化。用 MAPK 激酶激酶(Mos)的 mRNA 注射使 MAPK 磷酸化得以维持的卵,就像完整的卵一样,在受精或 IP3 注射时会发生钙离子上升,并阻止随后的精子-卵融合。然而,Mos 表达的卵在钙离子上升停止后可以接受精子。相比之下,将 MAPK 激酶抑制剂(MEK)加入未受精的卵中会导致 MAPK 的去磷酸化而不会引起钙离子水平升高,并阻止精子-卵融合。受精后注射 Mos mRNA 使 MAPK 重新磷酸化恢复了精子吸引力,这是另一个依赖 MAPK 的事件,但不允许随后的精子-卵融合。因此,MAPK 的去磷酸化可能不可逆地阻断精子-卵融合,可逆地抑制精子吸引力。总之,我们的数据表明,分别依赖钙离子和 MAPK 的快速和晚期机制都确保了水母卵的多精入卵阻断。