{"title":"冷冻扫描电镜在血液学研究中的应用。","authors":"Irina Davidovich, Carina Levin, Yeshayahu Talmon","doi":"10.1111/jmi.13424","DOIUrl":null,"url":null,"abstract":"<p><p>Cryogenic scanning electron microscopy (cryo-SEM) is a powerful imaging technique used in cellular biology, providing high-resolution micrographs that show the complexity and dynamics of biological systems. The use of high-pressure freezing (HPF) for specimen fixation preserves cellular structures in their native, hydrated state, avoiding the artefacts introduced by conventional chemical fixation, while modern microscopes provide high-resolution imaging at low electron acceleration voltage, giving fine structural details. That makes cryo-SEM a unique tool for understanding cellular complexity. However, operating the SEM at cryogenic conditions requires careful optimisation of working parameters to avoid artefacts. In our work, we explore the potential of cryo-SEM for haematology and general cell studies. We discuss the impact of a combination of different signals and work distance on specimen appearance and present examples of studies on healthy human blood cells under physiological conditions. Our findings illustrate the breadth of information that can be obtained from these data, highlighting the technique's capacity to enhance our understanding of cellular biology.</p>","PeriodicalId":16484,"journal":{"name":"Journal of microscopy","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cryo-SEM in haematological research.\",\"authors\":\"Irina Davidovich, Carina Levin, Yeshayahu Talmon\",\"doi\":\"10.1111/jmi.13424\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cryogenic scanning electron microscopy (cryo-SEM) is a powerful imaging technique used in cellular biology, providing high-resolution micrographs that show the complexity and dynamics of biological systems. The use of high-pressure freezing (HPF) for specimen fixation preserves cellular structures in their native, hydrated state, avoiding the artefacts introduced by conventional chemical fixation, while modern microscopes provide high-resolution imaging at low electron acceleration voltage, giving fine structural details. That makes cryo-SEM a unique tool for understanding cellular complexity. However, operating the SEM at cryogenic conditions requires careful optimisation of working parameters to avoid artefacts. In our work, we explore the potential of cryo-SEM for haematology and general cell studies. We discuss the impact of a combination of different signals and work distance on specimen appearance and present examples of studies on healthy human blood cells under physiological conditions. Our findings illustrate the breadth of information that can be obtained from these data, highlighting the technique's capacity to enhance our understanding of cellular biology.</p>\",\"PeriodicalId\":16484,\"journal\":{\"name\":\"Journal of microscopy\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2025-05-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of microscopy\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1111/jmi.13424\",\"RegionNum\":4,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROSCOPY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of microscopy","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1111/jmi.13424","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROSCOPY","Score":null,"Total":0}
Cryogenic scanning electron microscopy (cryo-SEM) is a powerful imaging technique used in cellular biology, providing high-resolution micrographs that show the complexity and dynamics of biological systems. The use of high-pressure freezing (HPF) for specimen fixation preserves cellular structures in their native, hydrated state, avoiding the artefacts introduced by conventional chemical fixation, while modern microscopes provide high-resolution imaging at low electron acceleration voltage, giving fine structural details. That makes cryo-SEM a unique tool for understanding cellular complexity. However, operating the SEM at cryogenic conditions requires careful optimisation of working parameters to avoid artefacts. In our work, we explore the potential of cryo-SEM for haematology and general cell studies. We discuss the impact of a combination of different signals and work distance on specimen appearance and present examples of studies on healthy human blood cells under physiological conditions. Our findings illustrate the breadth of information that can be obtained from these data, highlighting the technique's capacity to enhance our understanding of cellular biology.
期刊介绍:
The Journal of Microscopy is the oldest journal dedicated to the science of microscopy and the only peer-reviewed publication of the Royal Microscopical Society. It publishes papers that report on the very latest developments in microscopy such as advances in microscopy techniques or novel areas of application. The Journal does not seek to publish routine applications of microscopy or specimen preparation even though the submission may otherwise have a high scientific merit.
The scope covers research in the physical and biological sciences and covers imaging methods using light, electrons, X-rays and other radiations as well as atomic force and near field techniques. Interdisciplinary research is welcome. Papers pertaining to microscopy are also welcomed on optical theory, spectroscopy, novel specimen preparation and manipulation methods and image recording, processing and analysis including dynamic analysis of living specimens.
Publication types include full papers, hot topic fast tracked communications and review articles. Authors considering submitting a review article should contact the editorial office first.