Serial block face scanning electron microscopy in cell biology: Applications and technology
•SBFSEM was introduced in 2004 and has become a major tool for three-dimensional electron microscopy.•SBFSEM has become widespread in connectomics, cellular and matrix biology.•Problems with the technique are being overcome by advances in technology.•Data analysis represents a bottleneck but advance...
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Veröffentlicht in: | Tissue & cell 2019-04, Vol.57, p.111-122 |
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description | •SBFSEM was introduced in 2004 and has become a major tool for three-dimensional electron microscopy.•SBFSEM has become widespread in connectomics, cellular and matrix biology.•Problems with the technique are being overcome by advances in technology.•Data analysis represents a bottleneck but advances in computation and crowd-sourcing are set to improve this.
Three-dimensional electron microscopy (3DEM) is an imaging field containing several powerful modalities such as serial section transmission electron microscopy and electron tomography. However, large-scale 3D studies of biological ultrastructure on a cellular scale have historically been hampered by the difficulty of available techniques. Serial block face scanning electron microscopy (SBFSEM) is a 3DEM technique, developed in 2004, which has greatly increased the reliability, availability and throughput of 3DEM. SBFSEM allows for 3D imaging at resolutions high enough to resolve membranes and small vesicles whilst having the capability to collect data with a large field of view. Since its introduction it has become a major tool for ultrastructural investigation and has been applied in the study of many biological fields, such as connectomics, cellular and matrix biology. In this review, we will discuss biological SBFSEM from a technical standpoint, with a focus on cellular applications and also subsequent image analysis techniques. |
doi_str_mv | 10.1016/j.tice.2018.08.011 |
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Three-dimensional electron microscopy (3DEM) is an imaging field containing several powerful modalities such as serial section transmission electron microscopy and electron tomography. However, large-scale 3D studies of biological ultrastructure on a cellular scale have historically been hampered by the difficulty of available techniques. Serial block face scanning electron microscopy (SBFSEM) is a 3DEM technique, developed in 2004, which has greatly increased the reliability, availability and throughput of 3DEM. SBFSEM allows for 3D imaging at resolutions high enough to resolve membranes and small vesicles whilst having the capability to collect data with a large field of view. Since its introduction it has become a major tool for ultrastructural investigation and has been applied in the study of many biological fields, such as connectomics, cellular and matrix biology. In this review, we will discuss biological SBFSEM from a technical standpoint, with a focus on cellular applications and also subsequent image analysis techniques.</description><identifier>ISSN: 0040-8166</identifier><identifier>EISSN: 1532-3072</identifier><identifier>DOI: 10.1016/j.tice.2018.08.011</identifier><identifier>PMID: 30220487</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Biology ; Electron microscopes ; Field of view ; Historical account ; Image analysis ; Image processing ; Medical imaging ; Membranes ; SBEM ; SBF-SEM ; SBFSEM ; Scanning electron microscopy ; Serial block face scanning electron microscopy ; Transmission electron microscopy ; Ultrastructure</subject><ispartof>Tissue & cell, 2019-04, Vol.57, p.111-122</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Apr 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-27b8e36351ecebc70ad7b37e9b853df79cb13673525d10e2290595bc009d33fc3</citedby><cites>FETCH-LOGICAL-c494t-27b8e36351ecebc70ad7b37e9b853df79cb13673525d10e2290595bc009d33fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tice.2018.08.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30220487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smith, David</creatorcontrib><creatorcontrib>Starborg, Tobias</creatorcontrib><title>Serial block face scanning electron microscopy in cell biology: Applications and technology</title><title>Tissue & cell</title><addtitle>Tissue Cell</addtitle><description>•SBFSEM was introduced in 2004 and has become a major tool for three-dimensional electron microscopy.•SBFSEM has become widespread in connectomics, cellular and matrix biology.•Problems with the technique are being overcome by advances in technology.•Data analysis represents a bottleneck but advances in computation and crowd-sourcing are set to improve this.
Three-dimensional electron microscopy (3DEM) is an imaging field containing several powerful modalities such as serial section transmission electron microscopy and electron tomography. However, large-scale 3D studies of biological ultrastructure on a cellular scale have historically been hampered by the difficulty of available techniques. Serial block face scanning electron microscopy (SBFSEM) is a 3DEM technique, developed in 2004, which has greatly increased the reliability, availability and throughput of 3DEM. SBFSEM allows for 3D imaging at resolutions high enough to resolve membranes and small vesicles whilst having the capability to collect data with a large field of view. Since its introduction it has become a major tool for ultrastructural investigation and has been applied in the study of many biological fields, such as connectomics, cellular and matrix biology. In this review, we will discuss biological SBFSEM from a technical standpoint, with a focus on cellular applications and also subsequent image analysis techniques.</description><subject>Biology</subject><subject>Electron microscopes</subject><subject>Field of view</subject><subject>Historical account</subject><subject>Image analysis</subject><subject>Image processing</subject><subject>Medical imaging</subject><subject>Membranes</subject><subject>SBEM</subject><subject>SBF-SEM</subject><subject>SBFSEM</subject><subject>Scanning electron microscopy</subject><subject>Serial block face scanning electron microscopy</subject><subject>Transmission electron microscopy</subject><subject>Ultrastructure</subject><issn>0040-8166</issn><issn>1532-3072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kE1v1DAQhq0KRLeFP9ADssSllyxjO4kTxKWq-iVV4gCcOFjOZFK8ZO1gZyvtv8fpthw4II00h3nm1czD2JmAtQBRf9ysZ4e0liCaNeQS4oitRKVkoUDLV2wFUELRiLo-ZicpbQBAl0K_YccKpISy0Sv24ytFZ0fejQF_8cEi8YTWe-cfOI2Ecwyebx3GkDBMe-48Rxoz78IYHvaf-MU0jQ7t7IJP3Pqez4Q__dPwLXs92DHRu-d-yr5fX327vC3uv9zcXV7cF1i25VxI3TWkalUJQupQg-11pzS1XVOpftAtdkLVWlWy6gWQlC1UbdUhQNsrNaA6ZeeH3CmG3ztKs9m6tFxpPYVdMlJAI-umVjKjH_5BN2EXfb7OSCkaBVmsyJQ8UMvbKdJgpui2Nu6NALOoNxuzqDeLegO5npbeP0fvui31f1deXGfg8wGg7OLRUTQJHXmk3sUs2vTB_S__D0_elEs</recordid><startdate>201904</startdate><enddate>201904</enddate><creator>Smith, David</creator><creator>Starborg, Tobias</creator><general>Elsevier Ltd</general><general>Elsevier Science Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201904</creationdate><title>Serial block face scanning electron microscopy in cell biology: Applications and technology</title><author>Smith, David ; Starborg, Tobias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-27b8e36351ecebc70ad7b37e9b853df79cb13673525d10e2290595bc009d33fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biology</topic><topic>Electron microscopes</topic><topic>Field of view</topic><topic>Historical account</topic><topic>Image analysis</topic><topic>Image processing</topic><topic>Medical imaging</topic><topic>Membranes</topic><topic>SBEM</topic><topic>SBF-SEM</topic><topic>SBFSEM</topic><topic>Scanning electron microscopy</topic><topic>Serial block face scanning electron microscopy</topic><topic>Transmission electron microscopy</topic><topic>Ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, David</creatorcontrib><creatorcontrib>Starborg, Tobias</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Tissue & cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, David</au><au>Starborg, Tobias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serial block face scanning electron microscopy in cell biology: Applications and technology</atitle><jtitle>Tissue & cell</jtitle><addtitle>Tissue Cell</addtitle><date>2019-04</date><risdate>2019</risdate><volume>57</volume><spage>111</spage><epage>122</epage><pages>111-122</pages><issn>0040-8166</issn><eissn>1532-3072</eissn><abstract>•SBFSEM was introduced in 2004 and has become a major tool for three-dimensional electron microscopy.•SBFSEM has become widespread in connectomics, cellular and matrix biology.•Problems with the technique are being overcome by advances in technology.•Data analysis represents a bottleneck but advances in computation and crowd-sourcing are set to improve this.
Three-dimensional electron microscopy (3DEM) is an imaging field containing several powerful modalities such as serial section transmission electron microscopy and electron tomography. However, large-scale 3D studies of biological ultrastructure on a cellular scale have historically been hampered by the difficulty of available techniques. Serial block face scanning electron microscopy (SBFSEM) is a 3DEM technique, developed in 2004, which has greatly increased the reliability, availability and throughput of 3DEM. SBFSEM allows for 3D imaging at resolutions high enough to resolve membranes and small vesicles whilst having the capability to collect data with a large field of view. Since its introduction it has become a major tool for ultrastructural investigation and has been applied in the study of many biological fields, such as connectomics, cellular and matrix biology. In this review, we will discuss biological SBFSEM from a technical standpoint, with a focus on cellular applications and also subsequent image analysis techniques.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>30220487</pmid><doi>10.1016/j.tice.2018.08.011</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biology Electron microscopes Field of view Historical account Image analysis Image processing Medical imaging Membranes SBEM SBF-SEM SBFSEM Scanning electron microscopy Serial block face scanning electron microscopy Transmission electron microscopy Ultrastructure |
title | Serial block face scanning electron microscopy in cell biology: Applications and technology |
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