Kon Shinnosuke, Takaku Akio, Toyama Fubito, Takayama-Watanabe Eriko, Watanabe Akihiko
Faculty of Science, Yamagata University, 1-4-12 Kojirakawa, Yamagata, Japan.
Int J Dev Biol. 2019;63(11-12):589-595. doi: 10.1387/ijdb.190092aw.
The acrosome reaction is induced in the sperm of Cynops pyrrhogaster immediately in response to a ligand protein called acrosome reaction-inducing substance (ARIS) in the egg jelly at fertilization, whereas a spontaneous acrosome reaction occurs time-dependently in correlation with the decline of sperm quality for fertilization. The ARIS-induced acrosome reaction was recently found to be mediated by TRPV4 in association with the NMDA type glutamate receptor, although the intracellular mediators for the acrosome reaction are largely unclear. In the present study, spontaneous acrosome reaction was significantly inhibited by Ni, RN1734, and diltiazem, which blocks Cav3.2, TRPV4 or TRPM8, and the cyclic nucleotide-gated channel, respectively. In contrast, expression of Ca-activated transmembrane and soluble adenylyl cyclases was detected in the sperm of C. pyrrhogaster by reverse transcription-polymerase chain reaction. Activator of transmembrane or soluble adenylyl cyclases (forskolin or HCO ) independently promoted spontaneous acrosome reaction, while an inhibitor of each enzyme (MD12330A or KH7) inhibited it only in the sperm with high potential for spontaneous acrosome reaction. An inhibitor of protein kinase A (H89) inhibited spontaneous acrosome reaction in a manner independent of sperm potential for spontaneous acrosome reaction. Surprisingly, KH7 significantly inhibited ARIS-induced acrosome reaction, but its effect was seen in a small percentage of sperm. H89 had no effect on ARIS-induced acrosome reaction. These results suggest that C. pyrrhogaster sperm possess multiple intracellular pathways for acrosome reaction, involving Ca permeable channels, adenylyl cyclases and PKA, and that two pathways having distinct dependencies on adenylyl cyclases may contribute to ARIS-induced acrosome reaction at fertilization.
在受精时,日本林蛙精子会立即响应卵胶中一种名为顶体反应诱导物质(ARIS)的配体蛋白而引发顶体反应,而自发顶体反应则与受精精子质量的下降呈时间依赖性相关。最近发现,ARIS诱导的顶体反应是由TRPV4与NMDA型谷氨酸受体共同介导的,尽管顶体反应的细胞内介质在很大程度上尚不清楚。在本研究中,镍、RN1734和地尔硫䓬分别阻断Cav3.2、TRPV4或TRPM8以及环核苷酸门控通道,可显著抑制自发顶体反应。相比之下,通过逆转录聚合酶链反应在日本林蛙精子中检测到了钙激活的跨膜和可溶性腺苷酸环化酶的表达。跨膜或可溶性腺苷酸环化酶的激活剂(福斯可林或HCO)分别促进自发顶体反应,而每种酶的抑制剂(MD12330A或KH7)仅在具有高自发顶体反应潜力的精子中抑制该反应。蛋白激酶A抑制剂(H89)以与精子自发顶体反应潜力无关的方式抑制自发顶体反应。令人惊讶的是,KH7显著抑制ARIS诱导的顶体反应,但其作用仅在一小部分精子中可见。H89对ARIS诱导的顶体反应没有影响。这些结果表明,日本林蛙精子具有多种顶体反应的细胞内途径,涉及钙通透通道、腺苷酸环化酶和蛋白激酶A,并且两条对腺苷酸环化酶具有不同依赖性的途径可能有助于受精时ARIS诱导的顶体反应。