Cardiac Light-Sheet Fluorescent Microscopy for Multi-Scale and Rapid Imaging of Architecture and Function
Light Sheet Fluorescence Microscopy (LSFM) enables multi-dimensional and multi-scale imaging via illuminating specimens with a separate thin sheet of laser. It allows rapid plane illumination for reduced photo-damage and superior axial resolution and contrast. We hereby demonstrate cardiac LSFM (c-L...
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Veröffentlicht in: | Scientific reports 2016-03, Vol.6 (1), p.22489-22489, Article 22489 |
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creator | Fei, Peng Lee, Juhyun Packard, René R. Sevag Sereti, Konstantina-Ioanna Xu, Hao Ma, Jianguo Ding, Yichen Kang, Hanul Chen, Harrison Sung, Kevin Kulkarni, Rajan Ardehali, Reza Kuo, C.-C. Jay Xu, Xiaolei Ho, Chih-Ming Hsiai, Tzung K. |
description | Light Sheet Fluorescence Microscopy (LSFM) enables multi-dimensional and multi-scale imaging via illuminating specimens with a separate thin sheet of laser. It allows rapid plane illumination for reduced photo-damage and superior axial resolution and contrast. We hereby demonstrate cardiac LSFM (c-LSFM) imaging to assess the functional architecture of zebrafish embryos with a retrospective cardiac synchronization algorithm for four-dimensional reconstruction (3-D space + time). By combining our approach with tissue clearing techniques, we reveal the entire cardiac structures and hypertrabeculation of adult zebrafish hearts in response to doxorubicin treatment. By integrating the resolution enhancement technique with c-LSFM to increase the resolving power under a large field-of-view, we demonstrate the use of low power objective to resolve the entire architecture of large-scale neonatal mouse hearts, revealing the helical orientation of individual myocardial fibers. Therefore, our c-LSFM imaging approach provides multi-scale visualization of architecture and function to drive cardiovascular research with translational implication in congenital heart diseases. |
doi_str_mv | 10.1038/srep22489 |
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Sevag ; Sereti, Konstantina-Ioanna ; Xu, Hao ; Ma, Jianguo ; Ding, Yichen ; Kang, Hanul ; Chen, Harrison ; Sung, Kevin ; Kulkarni, Rajan ; Ardehali, Reza ; Kuo, C.-C. Jay ; Xu, Xiaolei ; Ho, Chih-Ming ; Hsiai, Tzung K.</creator><creatorcontrib>Fei, Peng ; Lee, Juhyun ; Packard, René R. Sevag ; Sereti, Konstantina-Ioanna ; Xu, Hao ; Ma, Jianguo ; Ding, Yichen ; Kang, Hanul ; Chen, Harrison ; Sung, Kevin ; Kulkarni, Rajan ; Ardehali, Reza ; Kuo, C.-C. Jay ; Xu, Xiaolei ; Ho, Chih-Ming ; Hsiai, Tzung K.</creatorcontrib><description>Light Sheet Fluorescence Microscopy (LSFM) enables multi-dimensional and multi-scale imaging via illuminating specimens with a separate thin sheet of laser. It allows rapid plane illumination for reduced photo-damage and superior axial resolution and contrast. We hereby demonstrate cardiac LSFM (c-LSFM) imaging to assess the functional architecture of zebrafish embryos with a retrospective cardiac synchronization algorithm for four-dimensional reconstruction (3-D space + time). By combining our approach with tissue clearing techniques, we reveal the entire cardiac structures and hypertrabeculation of adult zebrafish hearts in response to doxorubicin treatment. By integrating the resolution enhancement technique with c-LSFM to increase the resolving power under a large field-of-view, we demonstrate the use of low power objective to resolve the entire architecture of large-scale neonatal mouse hearts, revealing the helical orientation of individual myocardial fibers. Therefore, our c-LSFM imaging approach provides multi-scale visualization of architecture and function to drive cardiovascular research with translational implication in congenital heart diseases.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep22489</identifier><identifier>PMID: 26935567</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>639/166/985 ; 639/624/1107/328/2237 ; Algorithms ; Animals ; Animals, Genetically Modified ; Cardiovascular diseases ; Coronary artery disease ; Doxorubicin ; Doxorubicin - pharmacology ; Embryos ; Fibers ; Fish ; Fluorescence microscopy ; Heart ; Heart diseases ; Humanities and Social Sciences ; Illumination ; Image Processing, Computer-Assisted - methods ; Medical imaging ; Mice ; Microscopy ; Microscopy, Fluorescence - methods ; multidisciplinary ; Myocardium - cytology ; Myocardium - metabolism ; Neonates ; Pharmaceuticals ; Science ; Synchronization ; Zebrafish - metabolism</subject><ispartof>Scientific reports, 2016-03, Vol.6 (1), p.22489-22489, Article 22489</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Mar 2016</rights><rights>Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-1b06bb8c8b68d0df079e5985d954382bfd51410073a226c00055e8590e8f26f33</citedby><cites>FETCH-LOGICAL-c438t-1b06bb8c8b68d0df079e5985d954382bfd51410073a226c00055e8590e8f26f33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776137/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776137/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26935567$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fei, Peng</creatorcontrib><creatorcontrib>Lee, Juhyun</creatorcontrib><creatorcontrib>Packard, René R. Sevag</creatorcontrib><creatorcontrib>Sereti, Konstantina-Ioanna</creatorcontrib><creatorcontrib>Xu, Hao</creatorcontrib><creatorcontrib>Ma, Jianguo</creatorcontrib><creatorcontrib>Ding, Yichen</creatorcontrib><creatorcontrib>Kang, Hanul</creatorcontrib><creatorcontrib>Chen, Harrison</creatorcontrib><creatorcontrib>Sung, Kevin</creatorcontrib><creatorcontrib>Kulkarni, Rajan</creatorcontrib><creatorcontrib>Ardehali, Reza</creatorcontrib><creatorcontrib>Kuo, C.-C. Jay</creatorcontrib><creatorcontrib>Xu, Xiaolei</creatorcontrib><creatorcontrib>Ho, Chih-Ming</creatorcontrib><creatorcontrib>Hsiai, Tzung K.</creatorcontrib><title>Cardiac Light-Sheet Fluorescent Microscopy for Multi-Scale and Rapid Imaging of Architecture and Function</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Light Sheet Fluorescence Microscopy (LSFM) enables multi-dimensional and multi-scale imaging via illuminating specimens with a separate thin sheet of laser. It allows rapid plane illumination for reduced photo-damage and superior axial resolution and contrast. We hereby demonstrate cardiac LSFM (c-LSFM) imaging to assess the functional architecture of zebrafish embryos with a retrospective cardiac synchronization algorithm for four-dimensional reconstruction (3-D space + time). By combining our approach with tissue clearing techniques, we reveal the entire cardiac structures and hypertrabeculation of adult zebrafish hearts in response to doxorubicin treatment. By integrating the resolution enhancement technique with c-LSFM to increase the resolving power under a large field-of-view, we demonstrate the use of low power objective to resolve the entire architecture of large-scale neonatal mouse hearts, revealing the helical orientation of individual myocardial fibers. Therefore, our c-LSFM imaging approach provides multi-scale visualization of architecture and function to drive cardiovascular research with translational implication in congenital heart diseases.</description><subject>639/166/985</subject><subject>639/624/1107/328/2237</subject><subject>Algorithms</subject><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Cardiovascular diseases</subject><subject>Coronary artery disease</subject><subject>Doxorubicin</subject><subject>Doxorubicin - pharmacology</subject><subject>Embryos</subject><subject>Fibers</subject><subject>Fish</subject><subject>Fluorescence microscopy</subject><subject>Heart</subject><subject>Heart diseases</subject><subject>Humanities and Social Sciences</subject><subject>Illumination</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Medical imaging</subject><subject>Mice</subject><subject>Microscopy</subject><subject>Microscopy, Fluorescence - methods</subject><subject>multidisciplinary</subject><subject>Myocardium - cytology</subject><subject>Myocardium - metabolism</subject><subject>Neonates</subject><subject>Pharmaceuticals</subject><subject>Science</subject><subject>Synchronization</subject><subject>Zebrafish - metabolism</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNplkV1rFDEYhYMottRe-Ack4I0WRvMx-boRyuLWwhbB6nXIZDKzKbPJmGSE_nuzbF1WzU0C5-HkPe8B4DVGHzCi8mNObiakleoZOCeoZQ2hhDw_eZ-By5wfUD2MqBarl-CMcEUZ4-Ic-JVJvTcWbvy4Lc391rkC19MSk8vWhQLvvE0x2zg_wiEmeLdMxTf31kwOmtDDb2b2PbzdmdGHEcYBXie79cXZsqQDsV6CLT6GV-DFYKbsLp_uC_Bj_fn76kuz-Xpzu7reNLalsjS4Q7zrpJUdlz3qBySUY0qyXrGqk27oGW4xQoIaQrjdp2JOMoWcHAgfKL0Anw6-89LtXL8Pkcyk5-R3Jj3qaLz-Wwl-q8f4S7dCcExFNXj3ZJDiz8Xlone-7mKaTHBxyRoLgSRnXKqKvv0HfYhLCjWexlJJgahSbaXeH6j9Jmtdw3EYjPS-Q33ssLJvTqc_kn8aq8DVAchVCqNLJ1_-5_YbdMulkg</recordid><startdate>20160303</startdate><enddate>20160303</enddate><creator>Fei, Peng</creator><creator>Lee, Juhyun</creator><creator>Packard, René R. 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Sevag</au><au>Sereti, Konstantina-Ioanna</au><au>Xu, Hao</au><au>Ma, Jianguo</au><au>Ding, Yichen</au><au>Kang, Hanul</au><au>Chen, Harrison</au><au>Sung, Kevin</au><au>Kulkarni, Rajan</au><au>Ardehali, Reza</au><au>Kuo, C.-C. Jay</au><au>Xu, Xiaolei</au><au>Ho, Chih-Ming</au><au>Hsiai, Tzung K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiac Light-Sheet Fluorescent Microscopy for Multi-Scale and Rapid Imaging of Architecture and Function</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2016-03-03</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><spage>22489</spage><epage>22489</epage><pages>22489-22489</pages><artnum>22489</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Light Sheet Fluorescence Microscopy (LSFM) enables multi-dimensional and multi-scale imaging via illuminating specimens with a separate thin sheet of laser. It allows rapid plane illumination for reduced photo-damage and superior axial resolution and contrast. We hereby demonstrate cardiac LSFM (c-LSFM) imaging to assess the functional architecture of zebrafish embryos with a retrospective cardiac synchronization algorithm for four-dimensional reconstruction (3-D space + time). By combining our approach with tissue clearing techniques, we reveal the entire cardiac structures and hypertrabeculation of adult zebrafish hearts in response to doxorubicin treatment. By integrating the resolution enhancement technique with c-LSFM to increase the resolving power under a large field-of-view, we demonstrate the use of low power objective to resolve the entire architecture of large-scale neonatal mouse hearts, revealing the helical orientation of individual myocardial fibers. Therefore, our c-LSFM imaging approach provides multi-scale visualization of architecture and function to drive cardiovascular research with translational implication in congenital heart diseases.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26935567</pmid><doi>10.1038/srep22489</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 639/166/985 639/624/1107/328/2237 Algorithms Animals Animals, Genetically Modified Cardiovascular diseases Coronary artery disease Doxorubicin Doxorubicin - pharmacology Embryos Fibers Fish Fluorescence microscopy Heart Heart diseases Humanities and Social Sciences Illumination Image Processing, Computer-Assisted - methods Medical imaging Mice Microscopy Microscopy, Fluorescence - methods multidisciplinary Myocardium - cytology Myocardium - metabolism Neonates Pharmaceuticals Science Synchronization Zebrafish - metabolism |
title | Cardiac Light-Sheet Fluorescent Microscopy for Multi-Scale and Rapid Imaging of Architecture and Function |
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