Detection of mitochondrial fission with orientation-dependent optical Fourier filters
We utilize a recently developed optical imaging method based on Fourier processing with Gabor-like filters to detect changes in light scattering resulting from alterations in mitochondrial structure in endothelial cells undergoing apoptosis. Imaging based on Gabor filters shows a significant decreas...
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Veröffentlicht in: | Cytometry. Part A 2011-02, Vol.79A (2), p.137-148 |
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creator | Pasternack, Robert M Zheng, Jing-Yi Boustany, Nada N |
description | We utilize a recently developed optical imaging method based on Fourier processing with Gabor-like filters to detect changes in light scattering resulting from alterations in mitochondrial structure in endothelial cells undergoing apoptosis. Imaging based on Gabor filters shows a significant decrease in the orientation of subcellular organelles at 60 to 100 minutes following apoptosis induction and concomitant with mitochondrial fragmentation observed by fluorescence. The optical scatter changes can be detected at low resolution at the whole cell level. At high resolution, we combine fluorescence imaging of the mitochondria with optical Fourier-based imaging to demonstrate that the dynamic decrease in organelle orientation measured by optical Gabor filtering is spatially associated with fluorescent mitochondria and remains largely absent from nonfluorescent subcellular regions. These results provide strong evidence that the optical Gabor responses track mitochondrial fission during apoptosis and can be used to provide label-free, rapid monitoring of this morphological process within single cells. © 2011 International Society for Advancement of Cytometry |
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Imaging based on Gabor filters shows a significant decrease in the orientation of subcellular organelles at 60 to 100 minutes following apoptosis induction and concomitant with mitochondrial fragmentation observed by fluorescence. The optical scatter changes can be detected at low resolution at the whole cell level. At high resolution, we combine fluorescence imaging of the mitochondria with optical Fourier-based imaging to demonstrate that the dynamic decrease in organelle orientation measured by optical Gabor filtering is spatially associated with fluorescent mitochondria and remains largely absent from nonfluorescent subcellular regions. 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Part A</title><addtitle>Cytometry A</addtitle><description>We utilize a recently developed optical imaging method based on Fourier processing with Gabor-like filters to detect changes in light scattering resulting from alterations in mitochondrial structure in endothelial cells undergoing apoptosis. Imaging based on Gabor filters shows a significant decrease in the orientation of subcellular organelles at 60 to 100 minutes following apoptosis induction and concomitant with mitochondrial fragmentation observed by fluorescence. The optical scatter changes can be detected at low resolution at the whole cell level. At high resolution, we combine fluorescence imaging of the mitochondria with optical Fourier-based imaging to demonstrate that the dynamic decrease in organelle orientation measured by optical Gabor filtering is spatially associated with fluorescent mitochondria and remains largely absent from nonfluorescent subcellular regions. These results provide strong evidence that the optical Gabor responses track mitochondrial fission during apoptosis and can be used to provide label-free, rapid monitoring of this morphological process within single cells. © 2011 International Society for Advancement of Cytometry</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - physiology</subject><subject>Cattle</subject><subject>Cells, Cultured</subject><subject>Cytometry</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - cytology</subject><subject>Endothelial Cells - ultrastructure</subject><subject>Filters</subject><subject>Filtration - instrumentation</subject><subject>Filtration - methods</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes - metabolism</subject><subject>Fourier Analysis</subject><subject>Image Interpretation, Computer-Assisted - instrumentation</subject><subject>Image Interpretation, Computer-Assisted - methods</subject><subject>imaging</subject><subject>Light scattering</subject><subject>microscopy</subject><subject>Mitochondria</subject><subject>Mitochondria - physiology</subject><subject>Mitochondria - ultrastructure</subject><subject>Optics and Photonics - instrumentation</subject><subject>Optics and Photonics - methods</subject><subject>Organelles</subject><subject>Organelles - physiology</subject><subject>Organelles - ultrastructure</subject><subject>Orientation - physiology</subject><subject>Scattering, Radiation</subject><subject>Staining and Labeling - methods</subject><subject>Subcellular Fractions - physiology</subject><issn>1552-4922</issn><issn>1552-4930</issn><issn>1552-4930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90DlPAzEQBWALgbg7atgOCjaMx3aWLVE4JSQKSEFlOT7AaLMOtqMo_x6HACWVx5pvXvEIOaIwoAB4oZc5DNQAKVC6QXapEFjzlsHm34y4Q_ZS-gBgAhhukx2kOBQAzS4ZX9tsdfahr4Krpj4H_R56E73qKudTWi0WPr9XIXrbZ7WStbEz25vyrcIse13obZiXfSwnXbYxHZAtp7pkD3_efTK-vXkZ3dePT3cPo6vHWnNsaT2cNAIRWnCcW0a1UcqARsPtBB0DDZo2gAxVwyatombIFQwV6paCcYI6tk9O17mzGD7nNmU59UnbrlO9DfMkL3nDGW8EK_LsX1naa9oGQGCh52uqY0gpWidn0U9VXBYkV5XLVeVSye_KCz_-SZ5Pptb84d-OC2BrsPCdXf4bJkevL0-_sSfrK6fK-i36JMfPCJQBbRm9FIJ9AciWlvc</recordid><startdate>201102</startdate><enddate>201102</enddate><creator>Pasternack, Robert M</creator><creator>Zheng, Jing-Yi</creator><creator>Boustany, Nada N</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201102</creationdate><title>Detection of mitochondrial fission with orientation-dependent optical Fourier filters</title><author>Pasternack, Robert M ; Zheng, Jing-Yi ; Boustany, Nada N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4291-6b7522090f44e31cdaad0c2d4eb2f30c0c170232a73b9a1d64a06a2c910df51f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - physiology</topic><topic>Cattle</topic><topic>Cells, Cultured</topic><topic>Cytometry</topic><topic>Endothelial cells</topic><topic>Endothelial Cells - cytology</topic><topic>Endothelial Cells - ultrastructure</topic><topic>Filters</topic><topic>Filtration - instrumentation</topic><topic>Filtration - methods</topic><topic>Fluorescence</topic><topic>Fluorescent Dyes - metabolism</topic><topic>Fourier Analysis</topic><topic>Image Interpretation, Computer-Assisted - instrumentation</topic><topic>Image Interpretation, Computer-Assisted - methods</topic><topic>imaging</topic><topic>Light scattering</topic><topic>microscopy</topic><topic>Mitochondria</topic><topic>Mitochondria - physiology</topic><topic>Mitochondria - ultrastructure</topic><topic>Optics and Photonics - instrumentation</topic><topic>Optics and Photonics - methods</topic><topic>Organelles</topic><topic>Organelles - physiology</topic><topic>Organelles - ultrastructure</topic><topic>Orientation - physiology</topic><topic>Scattering, Radiation</topic><topic>Staining and Labeling - methods</topic><topic>Subcellular Fractions - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pasternack, Robert M</creatorcontrib><creatorcontrib>Zheng, Jing-Yi</creatorcontrib><creatorcontrib>Boustany, Nada N</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cytometry. 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Imaging based on Gabor filters shows a significant decrease in the orientation of subcellular organelles at 60 to 100 minutes following apoptosis induction and concomitant with mitochondrial fragmentation observed by fluorescence. The optical scatter changes can be detected at low resolution at the whole cell level. At high resolution, we combine fluorescence imaging of the mitochondria with optical Fourier-based imaging to demonstrate that the dynamic decrease in organelle orientation measured by optical Gabor filtering is spatially associated with fluorescent mitochondria and remains largely absent from nonfluorescent subcellular regions. 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subjects | Animals Apoptosis Apoptosis - physiology Cattle Cells, Cultured Cytometry Endothelial cells Endothelial Cells - cytology Endothelial Cells - ultrastructure Filters Filtration - instrumentation Filtration - methods Fluorescence Fluorescent Dyes - metabolism Fourier Analysis Image Interpretation, Computer-Assisted - instrumentation Image Interpretation, Computer-Assisted - methods imaging Light scattering microscopy Mitochondria Mitochondria - physiology Mitochondria - ultrastructure Optics and Photonics - instrumentation Optics and Photonics - methods Organelles Organelles - physiology Organelles - ultrastructure Orientation - physiology Scattering, Radiation Staining and Labeling - methods Subcellular Fractions - physiology |
title | Detection of mitochondrial fission with orientation-dependent optical Fourier filters |
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