{"title":"纤维有机电化学晶体管揭示H2O2在植物体内相互增强和依赖蒸腾的传播及其变异潜力。","authors":"Hanqi Wen, Lingxuan Kong, Xinlu Zhu, Yansong Miao, Xing Sheng, Xiaodong Chen, Yuxin Liu, Peng Chen","doi":"10.1016/j.xinn.2025.100800","DOIUrl":null,"url":null,"abstract":"<p><p>Plants use hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) and variation potential (VP) waves as well as chemical transport by transpiration-driven xylem flow to facilitate cell signaling, cell-to-cell communication, and adaptation to environmental stresses. The underlying mechanisms and complex interplay among H<sub>2</sub>O<sub>2</sub>, VP, and transpiration are not clearly understood because of the lack of bioengineering tools for continuous <i>in planta</i> monitoring of the dynamic biological processes. Here, we tackle the challenge by developing microfiber-shaped organic electrochemical transistors (fOECTs) that can be threaded into the plants. The sensorized microfiber revealed that both H<sub>2</sub>O<sub>2</sub> and VP waves propagate faster toward the leaves than toward the roots because of the directional long-distance transport of H<sub>2</sub>O<sub>2</sub> in the xylem. In addition, the revealed interplays among VP, H<sub>2</sub>O<sub>2</sub>, and xylem flow strongly suggest a transpiration- and intensity-dependent H<sub>2</sub>O<sub>2</sub>-VP mutual-reinforcing propagation mechanism. The microfiber electronics offer a versatile platform for the <i>in situ</i> study of dynamic physiological processes in plants with high temporospatial resolution.</p>","PeriodicalId":36121,"journal":{"name":"The Innovation","volume":"6 5","pages":"100800"},"PeriodicalIF":33.2000,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12105492/pdf/","citationCount":"0","resultStr":"{\"title\":\"Mutually reinforcing and transpiration-dependent propagation of H<sub>2</sub>O<sub>2</sub> and variation potential in plants revealed by fiber organic electrochemical transistors.\",\"authors\":\"Hanqi Wen, Lingxuan Kong, Xinlu Zhu, Yansong Miao, Xing Sheng, Xiaodong Chen, Yuxin Liu, Peng Chen\",\"doi\":\"10.1016/j.xinn.2025.100800\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Plants use hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) and variation potential (VP) waves as well as chemical transport by transpiration-driven xylem flow to facilitate cell signaling, cell-to-cell communication, and adaptation to environmental stresses. The underlying mechanisms and complex interplay among H<sub>2</sub>O<sub>2</sub>, VP, and transpiration are not clearly understood because of the lack of bioengineering tools for continuous <i>in planta</i> monitoring of the dynamic biological processes. Here, we tackle the challenge by developing microfiber-shaped organic electrochemical transistors (fOECTs) that can be threaded into the plants. The sensorized microfiber revealed that both H<sub>2</sub>O<sub>2</sub> and VP waves propagate faster toward the leaves than toward the roots because of the directional long-distance transport of H<sub>2</sub>O<sub>2</sub> in the xylem. In addition, the revealed interplays among VP, H<sub>2</sub>O<sub>2</sub>, and xylem flow strongly suggest a transpiration- and intensity-dependent H<sub>2</sub>O<sub>2</sub>-VP mutual-reinforcing propagation mechanism. The microfiber electronics offer a versatile platform for the <i>in situ</i> study of dynamic physiological processes in plants with high temporospatial resolution.</p>\",\"PeriodicalId\":36121,\"journal\":{\"name\":\"The Innovation\",\"volume\":\"6 5\",\"pages\":\"100800\"},\"PeriodicalIF\":33.2000,\"publicationDate\":\"2025-01-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12105492/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Innovation\",\"FirstCategoryId\":\"95\",\"ListUrlMain\":\"https://doi.org/10.1016/j.xinn.2025.100800\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/5 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Innovation","FirstCategoryId":"95","ListUrlMain":"https://doi.org/10.1016/j.xinn.2025.100800","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/5 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Mutually reinforcing and transpiration-dependent propagation of H2O2 and variation potential in plants revealed by fiber organic electrochemical transistors.
Plants use hydrogen peroxide (H2O2) and variation potential (VP) waves as well as chemical transport by transpiration-driven xylem flow to facilitate cell signaling, cell-to-cell communication, and adaptation to environmental stresses. The underlying mechanisms and complex interplay among H2O2, VP, and transpiration are not clearly understood because of the lack of bioengineering tools for continuous in planta monitoring of the dynamic biological processes. Here, we tackle the challenge by developing microfiber-shaped organic electrochemical transistors (fOECTs) that can be threaded into the plants. The sensorized microfiber revealed that both H2O2 and VP waves propagate faster toward the leaves than toward the roots because of the directional long-distance transport of H2O2 in the xylem. In addition, the revealed interplays among VP, H2O2, and xylem flow strongly suggest a transpiration- and intensity-dependent H2O2-VP mutual-reinforcing propagation mechanism. The microfiber electronics offer a versatile platform for the in situ study of dynamic physiological processes in plants with high temporospatial resolution.
期刊介绍:
The Innovation is an interdisciplinary journal that aims to promote scientific application. It publishes cutting-edge research and high-quality reviews in various scientific disciplines, including physics, chemistry, materials, nanotechnology, biology, translational medicine, geoscience, and engineering. The journal adheres to the peer review and publishing standards of Cell Press journals.
The Innovation is committed to serving scientists and the public. It aims to publish significant advances promptly and provides a transparent exchange platform. The journal also strives to efficiently promote the translation from scientific discovery to technological achievements and rapidly disseminate scientific findings worldwide.
Indexed in the following databases, The Innovation has visibility in Scopus, Directory of Open Access Journals (DOAJ), Web of Science, Emerging Sources Citation Index (ESCI), PubMed Central, Compendex (previously Ei index), INSPEC, and CABI A&I.