Tian Li , Xiangna Yang , Haotian Sun , Hao Jing , Sinuo Bao , Yanfeng Hu , Wei Shi , Honglei Jia , Jisheng Li
{"title":"竞争离子摄取和转录调控:盐盐介导的盐对镉脱毒的协调双重机制","authors":"Tian Li , Xiangna Yang , Haotian Sun , Hao Jing , Sinuo Bao , Yanfeng Hu , Wei Shi , Honglei Jia , Jisheng Li","doi":"10.1016/j.plaphy.2025.109939","DOIUrl":null,"url":null,"abstract":"<div><div>Cadmium (Cd), a highly toxic heavy metal, severely inhibits plant growth. Salt alleviates Cd stress in halophytes, however, the molecular mechanisms governing salt-mediated regulation of Cd toxicity remain poorly understood. This study elucidates the protective mechanism of NaCl in Cd-stressed <em>Suaeda salsa</em> seedlings. Cd exposure suppressed seedling growth and induced membrane lipid peroxidation. Conversely, NaCl application not only maintained normal growth but also effectively ameliorated Cd-induced phytotoxicity, potentially through osmotic adjustment mechanisms. Notably, using ion flux analysis, we found that NaCl attenuated Cd<sup>2+</sup> influx into root epidermal cells, thereby enhancing Cd resistance. Pharmacological inhibition studies confirmed that Na <sup>+</sup> competitively inhibits Cd<sup>2+</sup> uptake through shared channels/transporters. Furthermore, RT-qPCR gene expression profiling revealed that NaCl coordinately activated both ionic compartmentalization and efflux systems through upregulating plasma membrane-localized <em>SsSOS1</em> and tonoplast-associated <em>SsNHX1</em> for Na <sup>+</sup> extrusion and vacuolar sequestration, enhancing Cd<sup>2+</sup> compartmentalization via <em>SsCAX</em> and <em>SsVHA-B</em> mediated transport and maintaining cellular homeostasis through <em>SsHKT1</em> and <em>SsPIP</em>-mediated regulation of water and K<sup>+</sup> balance, or indirectly inhibit Cd<sup>2+</sup> influx. It reveals that salt weakens Cd<sup>2+</sup> influx and enhances Cd tolerance by activating a coordinated gene regulatory network in <em>Suaeda salsa</em>. This finding offers valuable insights into phytoremediation strategies for enhancing crop resilience in Cd-contaminated saline soils.</div></div>","PeriodicalId":20234,"journal":{"name":"Plant Physiology and Biochemistry","volume":"224 ","pages":"Article 109939"},"PeriodicalIF":6.1000,"publicationDate":"2025-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Competitive ion uptake and transcriptional regulation as a coordinated dual mechanism of NaCl-mediated cadmium detoxification in Suaeda salsa\",\"authors\":\"Tian Li , Xiangna Yang , Haotian Sun , Hao Jing , Sinuo Bao , Yanfeng Hu , Wei Shi , Honglei Jia , Jisheng Li\",\"doi\":\"10.1016/j.plaphy.2025.109939\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cadmium (Cd), a highly toxic heavy metal, severely inhibits plant growth. Salt alleviates Cd stress in halophytes, however, the molecular mechanisms governing salt-mediated regulation of Cd toxicity remain poorly understood. This study elucidates the protective mechanism of NaCl in Cd-stressed <em>Suaeda salsa</em> seedlings. Cd exposure suppressed seedling growth and induced membrane lipid peroxidation. Conversely, NaCl application not only maintained normal growth but also effectively ameliorated Cd-induced phytotoxicity, potentially through osmotic adjustment mechanisms. Notably, using ion flux analysis, we found that NaCl attenuated Cd<sup>2+</sup> influx into root epidermal cells, thereby enhancing Cd resistance. Pharmacological inhibition studies confirmed that Na <sup>+</sup> competitively inhibits Cd<sup>2+</sup> uptake through shared channels/transporters. Furthermore, RT-qPCR gene expression profiling revealed that NaCl coordinately activated both ionic compartmentalization and efflux systems through upregulating plasma membrane-localized <em>SsSOS1</em> and tonoplast-associated <em>SsNHX1</em> for Na <sup>+</sup> extrusion and vacuolar sequestration, enhancing Cd<sup>2+</sup> compartmentalization via <em>SsCAX</em> and <em>SsVHA-B</em> mediated transport and maintaining cellular homeostasis through <em>SsHKT1</em> and <em>SsPIP</em>-mediated regulation of water and K<sup>+</sup> balance, or indirectly inhibit Cd<sup>2+</sup> influx. It reveals that salt weakens Cd<sup>2+</sup> influx and enhances Cd tolerance by activating a coordinated gene regulatory network in <em>Suaeda salsa</em>. This finding offers valuable insights into phytoremediation strategies for enhancing crop resilience in Cd-contaminated saline soils.</div></div>\",\"PeriodicalId\":20234,\"journal\":{\"name\":\"Plant Physiology and Biochemistry\",\"volume\":\"224 \",\"pages\":\"Article 109939\"},\"PeriodicalIF\":6.1000,\"publicationDate\":\"2025-04-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Physiology and Biochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S098194282500467X\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology and Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S098194282500467X","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Competitive ion uptake and transcriptional regulation as a coordinated dual mechanism of NaCl-mediated cadmium detoxification in Suaeda salsa
Cadmium (Cd), a highly toxic heavy metal, severely inhibits plant growth. Salt alleviates Cd stress in halophytes, however, the molecular mechanisms governing salt-mediated regulation of Cd toxicity remain poorly understood. This study elucidates the protective mechanism of NaCl in Cd-stressed Suaeda salsa seedlings. Cd exposure suppressed seedling growth and induced membrane lipid peroxidation. Conversely, NaCl application not only maintained normal growth but also effectively ameliorated Cd-induced phytotoxicity, potentially through osmotic adjustment mechanisms. Notably, using ion flux analysis, we found that NaCl attenuated Cd2+ influx into root epidermal cells, thereby enhancing Cd resistance. Pharmacological inhibition studies confirmed that Na + competitively inhibits Cd2+ uptake through shared channels/transporters. Furthermore, RT-qPCR gene expression profiling revealed that NaCl coordinately activated both ionic compartmentalization and efflux systems through upregulating plasma membrane-localized SsSOS1 and tonoplast-associated SsNHX1 for Na + extrusion and vacuolar sequestration, enhancing Cd2+ compartmentalization via SsCAX and SsVHA-B mediated transport and maintaining cellular homeostasis through SsHKT1 and SsPIP-mediated regulation of water and K+ balance, or indirectly inhibit Cd2+ influx. It reveals that salt weakens Cd2+ influx and enhances Cd tolerance by activating a coordinated gene regulatory network in Suaeda salsa. This finding offers valuable insights into phytoremediation strategies for enhancing crop resilience in Cd-contaminated saline soils.
期刊介绍:
Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement.
Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB.
Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.