Multi-color electron microscopy by element-guided identification of cells, organelles and molecules
Cellular complexity is unraveled at nanometer resolution using electron microscopy (EM), but interpretation of macromolecular functionality is hampered by the difficulty in interpreting grey-scale images and the unidentified molecular content. We perform large-scale EM on mammalian tissue complement...
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Published in | Scientific reports Vol. 7; no. 1; p. 45970 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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07.04.2017
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Abstract | Cellular complexity is unraveled at nanometer resolution using electron microscopy (EM), but interpretation of macromolecular functionality is hampered by the difficulty in interpreting grey-scale images and the unidentified molecular content. We perform large-scale EM on mammalian tissue complemented with energy-dispersive X-ray analysis (EDX) to allow EM-data analysis based on elemental composition. Endogenous elements, labels (gold and cadmium-based nanoparticles) as well as stains are analyzed at ultrastructural resolution. This provides a wide palette of colors to paint the traditional grey-scale EM images for composition-based interpretation. Our proof-of-principle application of EM-EDX reveals that endocrine and exocrine vesicles exist in single cells in Islets of Langerhans. This highlights how elemental mapping reveals unbiased biomedical relevant information. Broad application of EM-EDX will further allow experimental analysis on large-scale tissue using endogenous elements, multiple stains, and multiple markers and thus brings nanometer-scale ‘color-EM’ as a promising tool to unravel molecular (de)regulation in biomedicine. |
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AbstractList | Cellular complexity is unraveled at nanometer resolution using electron microscopy (EM), but interpretation of macromolecular functionality is hampered by the difficulty in interpreting grey-scale images and the unidentified molecular content. We perform large-scale EM on mammalian tissue complemented with energy-dispersive X-ray analysis (EDX) to allow EM-data analysis based on elemental composition. Endogenous elements, labels (gold and cadmium-based nanoparticles) as well as stains are analyzed at ultrastructural resolution. This provides a wide palette of colors to paint the traditional grey-scale EM images for composition-based interpretation. Our proof-of-principle application of EM-EDX reveals that endocrine and exocrine vesicles exist in single cells in Islets of Langerhans. This highlights how elemental mapping reveals unbiased biomedical relevant information. Broad application of EM-EDX will further allow experimental analysis on large-scale tissue using endogenous elements, multiple stains, and multiple markers and thus brings nanometer-scale 'color-EM' as a promising tool to unravel molecular (de)regulation in biomedicine. Abstract Cellular complexity is unraveled at nanometer resolution using electron microscopy (EM), but interpretation of macromolecular functionality is hampered by the difficulty in interpreting grey-scale images and the unidentified molecular content. We perform large-scale EM on mammalian tissue complemented with energy-dispersive X-ray analysis (EDX) to allow EM-data analysis based on elemental composition. Endogenous elements, labels (gold and cadmium-based nanoparticles) as well as stains are analyzed at ultrastructural resolution. This provides a wide palette of colors to paint the traditional grey-scale EM images for composition-based interpretation. Our proof-of-principle application of EM-EDX reveals that endocrine and exocrine vesicles exist in single cells in Islets of Langerhans. This highlights how elemental mapping reveals unbiased biomedical relevant information. Broad application of EM-EDX will further allow experimental analysis on large-scale tissue using endogenous elements, multiple stains, and multiple markers and thus brings nanometer-scale ‘color-EM’ as a promising tool to unravel molecular (de)regulation in biomedicine. |
ArticleNumber | 45970 |
Author | de Boer, Pascal Kuipers, Jeroen Giepmans, Ben N. G. Scotuzzi, Marijke Wensveen, Dasha I. Hagen, Kees (C.) W. Hoogenboom, Jacob P. |
Author_xml | – sequence: 1 givenname: Marijke surname: Scotuzzi fullname: Scotuzzi, Marijke organization: Dept. Imaging Physics, Delft University of Technology – sequence: 2 givenname: Jeroen surname: Kuipers fullname: Kuipers, Jeroen organization: Dept. Cell Biology, University Medical Centre Groningen, University of Groningen – sequence: 3 givenname: Dasha I. surname: Wensveen fullname: Wensveen, Dasha I. organization: Dept. Imaging Physics, Delft University of Technology – sequence: 4 givenname: Pascal surname: de Boer fullname: de Boer, Pascal organization: Dept. Cell Biology, University Medical Centre Groningen, University of Groningen – sequence: 5 givenname: Kees (C.) W. surname: Hagen fullname: Hagen, Kees (C.) W. organization: Dept. Imaging Physics, Delft University of Technology – sequence: 6 givenname: Jacob P. surname: Hoogenboom fullname: Hoogenboom, Jacob P. email: j.p.hoogenboom@tudelft.nl organization: Dept. Imaging Physics, Delft University of Technology – sequence: 7 givenname: Ben N. G. surname: Giepmans fullname: Giepmans, Ben N. G. email: b.n.g.giepmans@umcg.nl organization: Dept. Cell Biology, University Medical Centre Groningen, University of Groningen |
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Title | Multi-color electron microscopy by element-guided identification of cells, organelles and molecules |
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