Atsuko Kageyama, Narumi Ogonuki, Takuya Wakai, Takafumi Namiki, Yui Kawata, Manabu Ozawa, Yasuhiro Yamada, Toshiyuki Fukada, Atsuo Ogura, Rafael A. Fissore, Naomi Kashiwazaki, Junya Ito
{"title":"卵母细胞锌转运体Slc39a10/Zip10是小鼠受精过程中锌火花的调节器。","authors":"Atsuko Kageyama, Narumi Ogonuki, Takuya Wakai, Takafumi Namiki, Yui Kawata, Manabu Ozawa, Yasuhiro Yamada, Toshiyuki Fukada, Atsuo Ogura, Rafael A. Fissore, Naomi Kashiwazaki, Junya Ito","doi":"10.1101/2024.09.11.612381","DOIUrl":null,"url":null,"abstract":"In all vertebrates studied to date, a rise(s) in intracellular calcium is indispensable for successful fertilization and further embryonic development. Recent studies demonstrated that zinc is ejected to the extracellular milieu, the 'zinc spark', and follows the first few calcium rises of fertilization. However, the role of the zinc sparks in fertilization and development, and the supporting influx mechanism(s) are unknown. In this study in mouse oocytes, we investigated the role of zinc transporters <em>Zip6/Slc39a6</em> and <em>Zip10/Slc39a10</em>. Zip10 mRNA or ZIP10 was expressed throughout folliculogenesis in oocyte or the plasma membrane, respectively. ZIP6 was also expressed in nuclear localization in oocytes and granulosa cells throughout folliculogenesis. The number of ovulated oocytes was examined in oocyte-specific <em>Zip6</em> (<em>Zip6<sup>d/d</sup></em>: <em>Zip6<sup>flox/flox</sup> Gdf9<sup>Cre/+</sup></em>) and <em>Zip10</em> (<em>Zip10<sup>d/d</sup></em>: <em>Zip10<sup>flox/flox</sup> Gdf9<sup>Cre/+</sup></em>) knockout mice, and no change was observed for either strain. <em>Zip10<sup>d/d</sup></em> oocytes matured and formed normal metaphase II spindles, but had lower labile zinc levels as suggested by the zinc indicator, Fluozin-3 intensity. The levels of zinc fluorescence intensity in the <em>Zip6<sup>d/d</sup></em> group were not different from the <em>Zip6<sup>f/f</sup></em>. Fertilization-induced calcium oscillations were present in both <em>Zip6<sup>d/d</sup></em> and <em>Zip10<sup>d/d</sup></em> oocytes, but zinc sparks were observed in <em>Zip6<sup>d/d</sup></em> but not in <em>Zip10<sup>d/d</sup></em> oocytes. Despite other events of egg activation proceeding normally in <em>Zip10<sup>d/d</sup></em> oocytes, embryo development into blastocysts was compromised. We show here for the first time that the zinc transporter ZIP10 contributes to zinc homeostasis in oocytes and embryos, highlighting the pivotal role of this divalent cation in early development.","PeriodicalId":501269,"journal":{"name":"bioRxiv - Developmental Biology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The oocyte zinc transporter Slc39a10/Zip10 is a regulator of zinc sparks during fertilization in mice.\",\"authors\":\"Atsuko Kageyama, Narumi Ogonuki, Takuya Wakai, Takafumi Namiki, Yui Kawata, Manabu Ozawa, Yasuhiro Yamada, Toshiyuki Fukada, Atsuo Ogura, Rafael A. Fissore, Naomi Kashiwazaki, Junya Ito\",\"doi\":\"10.1101/2024.09.11.612381\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In all vertebrates studied to date, a rise(s) in intracellular calcium is indispensable for successful fertilization and further embryonic development. Recent studies demonstrated that zinc is ejected to the extracellular milieu, the 'zinc spark', and follows the first few calcium rises of fertilization. However, the role of the zinc sparks in fertilization and development, and the supporting influx mechanism(s) are unknown. In this study in mouse oocytes, we investigated the role of zinc transporters <em>Zip6/Slc39a6</em> and <em>Zip10/Slc39a10</em>. Zip10 mRNA or ZIP10 was expressed throughout folliculogenesis in oocyte or the plasma membrane, respectively. ZIP6 was also expressed in nuclear localization in oocytes and granulosa cells throughout folliculogenesis. The number of ovulated oocytes was examined in oocyte-specific <em>Zip6</em> (<em>Zip6<sup>d/d</sup></em>: <em>Zip6<sup>flox/flox</sup> Gdf9<sup>Cre/+</sup></em>) and <em>Zip10</em> (<em>Zip10<sup>d/d</sup></em>: <em>Zip10<sup>flox/flox</sup> Gdf9<sup>Cre/+</sup></em>) knockout mice, and no change was observed for either strain. <em>Zip10<sup>d/d</sup></em> oocytes matured and formed normal metaphase II spindles, but had lower labile zinc levels as suggested by the zinc indicator, Fluozin-3 intensity. The levels of zinc fluorescence intensity in the <em>Zip6<sup>d/d</sup></em> group were not different from the <em>Zip6<sup>f/f</sup></em>. Fertilization-induced calcium oscillations were present in both <em>Zip6<sup>d/d</sup></em> and <em>Zip10<sup>d/d</sup></em> oocytes, but zinc sparks were observed in <em>Zip6<sup>d/d</sup></em> but not in <em>Zip10<sup>d/d</sup></em> oocytes. Despite other events of egg activation proceeding normally in <em>Zip10<sup>d/d</sup></em> oocytes, embryo development into blastocysts was compromised. We show here for the first time that the zinc transporter ZIP10 contributes to zinc homeostasis in oocytes and embryos, highlighting the pivotal role of this divalent cation in early development.\",\"PeriodicalId\":501269,\"journal\":{\"name\":\"bioRxiv - Developmental Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"bioRxiv - Developmental Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.09.11.612381\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Developmental Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.09.11.612381","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The oocyte zinc transporter Slc39a10/Zip10 is a regulator of zinc sparks during fertilization in mice.
In all vertebrates studied to date, a rise(s) in intracellular calcium is indispensable for successful fertilization and further embryonic development. Recent studies demonstrated that zinc is ejected to the extracellular milieu, the 'zinc spark', and follows the first few calcium rises of fertilization. However, the role of the zinc sparks in fertilization and development, and the supporting influx mechanism(s) are unknown. In this study in mouse oocytes, we investigated the role of zinc transporters Zip6/Slc39a6 and Zip10/Slc39a10. Zip10 mRNA or ZIP10 was expressed throughout folliculogenesis in oocyte or the plasma membrane, respectively. ZIP6 was also expressed in nuclear localization in oocytes and granulosa cells throughout folliculogenesis. The number of ovulated oocytes was examined in oocyte-specific Zip6 (Zip6d/d: Zip6flox/flox Gdf9Cre/+) and Zip10 (Zip10d/d: Zip10flox/flox Gdf9Cre/+) knockout mice, and no change was observed for either strain. Zip10d/d oocytes matured and formed normal metaphase II spindles, but had lower labile zinc levels as suggested by the zinc indicator, Fluozin-3 intensity. The levels of zinc fluorescence intensity in the Zip6d/d group were not different from the Zip6f/f. Fertilization-induced calcium oscillations were present in both Zip6d/d and Zip10d/d oocytes, but zinc sparks were observed in Zip6d/d but not in Zip10d/d oocytes. Despite other events of egg activation proceeding normally in Zip10d/d oocytes, embryo development into blastocysts was compromised. We show here for the first time that the zinc transporter ZIP10 contributes to zinc homeostasis in oocytes and embryos, highlighting the pivotal role of this divalent cation in early development.