{"title":"高动态和敏感的NEMOer钙指标成像内质网钙信号的兴奋性细胞","authors":"Wenjia Gu, Jia-Hui Chen, Yiyin Zhang, Zhirong Wang, Jia Li, Sijia Wang, Hanhan Zhang, Amin Jiang, Ziyi Zhong, Jiaxuan Zhang, Ze Xu, Panpan Liu, Chao Xi, Tingting Hou, Donald L. Gill, Dong Li, Yu Mu, Shi-Qiang Wang, Ai-Hui Tang, Youjun Wang","doi":"10.1038/s41467-025-58705-6","DOIUrl":null,"url":null,"abstract":"<p>The Endoplasmic/sarcoplasmic reticulum (ER/SR) is central to calcium (Ca<sup>2+</sup>) signaling, yet current genetically encoded Ca<sup>2+</sup> indicators (GECIs) cannot detect elementary Ca<sup>2+</sup> release events from ER/SR, particularly in muscle cells. Here, we report NEMOer, a set of organellar GECIs, to efficiently capture ER Ca<sup>2+</sup> dynamics with increased sensitivity and responsiveness. NEMOer indicators exhibit dynamic ranges an order of magnitude larger than G-CEPIA1er, enabling 2.7-fold more sensitive detection of Ca<sup>2+</sup> transients in both non-excitable and excitable cells. The ratiometric version further allows super-resolution monitoring of local ER Ca<sup>2+</sup> homeostasis and dynamics. Notably, NEMOer-f enabled the inaugural detection of Ca<sup>2+</sup> blinks, elementary Ca<sup>2+</sup> releasing signals from the SR of cardiomyocytes, as well as in vivo spontaneous SR Ca<sup>2+</sup> releases in zebrafish. In summary, the highly dynamic NEMOer sensors expand the repertoire of organellar Ca<sup>2+</sup> sensors that allow real-time monitoring of intricate Ca<sup>2+</sup> dynamics and homeostasis in live cells with high spatiotemporal resolution.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"116 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Highly dynamic and sensitive NEMOer calcium indicators for imaging ER calcium signals in excitable cells\",\"authors\":\"Wenjia Gu, Jia-Hui Chen, Yiyin Zhang, Zhirong Wang, Jia Li, Sijia Wang, Hanhan Zhang, Amin Jiang, Ziyi Zhong, Jiaxuan Zhang, Ze Xu, Panpan Liu, Chao Xi, Tingting Hou, Donald L. Gill, Dong Li, Yu Mu, Shi-Qiang Wang, Ai-Hui Tang, Youjun Wang\",\"doi\":\"10.1038/s41467-025-58705-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The Endoplasmic/sarcoplasmic reticulum (ER/SR) is central to calcium (Ca<sup>2+</sup>) signaling, yet current genetically encoded Ca<sup>2+</sup> indicators (GECIs) cannot detect elementary Ca<sup>2+</sup> release events from ER/SR, particularly in muscle cells. Here, we report NEMOer, a set of organellar GECIs, to efficiently capture ER Ca<sup>2+</sup> dynamics with increased sensitivity and responsiveness. NEMOer indicators exhibit dynamic ranges an order of magnitude larger than G-CEPIA1er, enabling 2.7-fold more sensitive detection of Ca<sup>2+</sup> transients in both non-excitable and excitable cells. The ratiometric version further allows super-resolution monitoring of local ER Ca<sup>2+</sup> homeostasis and dynamics. Notably, NEMOer-f enabled the inaugural detection of Ca<sup>2+</sup> blinks, elementary Ca<sup>2+</sup> releasing signals from the SR of cardiomyocytes, as well as in vivo spontaneous SR Ca<sup>2+</sup> releases in zebrafish. In summary, the highly dynamic NEMOer sensors expand the repertoire of organellar Ca<sup>2+</sup> sensors that allow real-time monitoring of intricate Ca<sup>2+</sup> dynamics and homeostasis in live cells with high spatiotemporal resolution.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"116 1\",\"pages\":\"\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-025-58705-6\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-58705-6","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Highly dynamic and sensitive NEMOer calcium indicators for imaging ER calcium signals in excitable cells
The Endoplasmic/sarcoplasmic reticulum (ER/SR) is central to calcium (Ca2+) signaling, yet current genetically encoded Ca2+ indicators (GECIs) cannot detect elementary Ca2+ release events from ER/SR, particularly in muscle cells. Here, we report NEMOer, a set of organellar GECIs, to efficiently capture ER Ca2+ dynamics with increased sensitivity and responsiveness. NEMOer indicators exhibit dynamic ranges an order of magnitude larger than G-CEPIA1er, enabling 2.7-fold more sensitive detection of Ca2+ transients in both non-excitable and excitable cells. The ratiometric version further allows super-resolution monitoring of local ER Ca2+ homeostasis and dynamics. Notably, NEMOer-f enabled the inaugural detection of Ca2+ blinks, elementary Ca2+ releasing signals from the SR of cardiomyocytes, as well as in vivo spontaneous SR Ca2+ releases in zebrafish. In summary, the highly dynamic NEMOer sensors expand the repertoire of organellar Ca2+ sensors that allow real-time monitoring of intricate Ca2+ dynamics and homeostasis in live cells with high spatiotemporal resolution.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.