Three-dimensional investigation and scoring of extracellular matrix remodeling during lung fibrosis using multiphoton microscopy
The organization of collagen during fibrotic processes is poorly characterized because of the lack of appropriate methodologies. Here we show that multimodal multiphoton microscopy provides novel insights into lung fibrosis. We characterize normal and fibrotic pulmonary tissue in the bleomycin model...
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Veröffentlicht in: | Microscopy research and technique 2007-02, Vol.70 (2), p.162-170 |
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creator | Pena, Ana-Maria Fabre, Aurélie Débarre, Delphine Marchal-Somme, Joëlle Crestani, Bruno Martin, Jean-Louis Beaurepaire, Emmanuel Schanne-Klein, Marie-Claire |
description | The organization of collagen during fibrotic processes is poorly characterized because of the lack of appropriate methodologies. Here we show that multimodal multiphoton microscopy provides novel insights into lung fibrosis. We characterize normal and fibrotic pulmonary tissue in the bleomycin model, and show that second‐harmonic generation by fibrillar collagen reveals the micrometer‐scale three‐dimensional spatial distribution of the fibrosis. We find that combined two‐photon excited fluorescence and second‐harmonic imaging of unstained lung tissue allows separating the inflammatory and fibrotic steps in this pathology, underlining characteristic features of fibroblastic foci in human Idiopathic Pulmonary Fibrosis samples. Finally, we propose phenomenological scores of lung fibrosis and we show that they unambiguously sort out control and treated mice, with a better sensitivity and reproducibility in the subpleural region. These results should be readily generalized to other organs, as an accurate method to assess extracellular matrix remodeling during fibrosis. Microsc. Res. Tech., 2007. © 2006 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jemt.20400 |
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Here we show that multimodal multiphoton microscopy provides novel insights into lung fibrosis. We characterize normal and fibrotic pulmonary tissue in the bleomycin model, and show that second‐harmonic generation by fibrillar collagen reveals the micrometer‐scale three‐dimensional spatial distribution of the fibrosis. We find that combined two‐photon excited fluorescence and second‐harmonic imaging of unstained lung tissue allows separating the inflammatory and fibrotic steps in this pathology, underlining characteristic features of fibroblastic foci in human Idiopathic Pulmonary Fibrosis samples. Finally, we propose phenomenological scores of lung fibrosis and we show that they unambiguously sort out control and treated mice, with a better sensitivity and reproducibility in the subpleural region. These results should be readily generalized to other organs, as an accurate method to assess extracellular matrix remodeling during fibrosis. Microsc. Res. 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Res. Tech</addtitle><description>The organization of collagen during fibrotic processes is poorly characterized because of the lack of appropriate methodologies. Here we show that multimodal multiphoton microscopy provides novel insights into lung fibrosis. We characterize normal and fibrotic pulmonary tissue in the bleomycin model, and show that second‐harmonic generation by fibrillar collagen reveals the micrometer‐scale three‐dimensional spatial distribution of the fibrosis. We find that combined two‐photon excited fluorescence and second‐harmonic imaging of unstained lung tissue allows separating the inflammatory and fibrotic steps in this pathology, underlining characteristic features of fibroblastic foci in human Idiopathic Pulmonary Fibrosis samples. Finally, we propose phenomenological scores of lung fibrosis and we show that they unambiguously sort out control and treated mice, with a better sensitivity and reproducibility in the subpleural region. These results should be readily generalized to other organs, as an accurate method to assess extracellular matrix remodeling during fibrosis. Microsc. Res. Tech., 2007. © 2006 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Bleomycin</subject><subject>collagen</subject><subject>Collagen - ultrastructure</subject><subject>Extracellular Matrix - ultrastructure</subject><subject>Humans</subject><subject>Lung - pathology</subject><subject>lung morphology</subject><subject>Macrophages, Alveolar - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Fluorescence, Multiphoton - methods</subject><subject>Pleura - pathology</subject><subject>Pulmonary Fibrosis - chemically induced</subject><subject>Pulmonary Fibrosis - pathology</subject><subject>second harmonic generation</subject><subject>three dimensional imaging</subject><issn>1059-910X</issn><issn>1097-0029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v1DAQxS0EoqVw4QOgnJBAShk7f5wcq6psQQscWMTeLK896brY8WInZffGR8dplnLjYnuef_OkmUfISwrnFIC9u0U3nDMoAR6RUwotz5PaPp7eVZu3FNYn5FmMtwCUVrR8Sk4op5wzXp2S36ttQMy1cdhH43tpM9PfYRzMjRxSncleZ1H5YPqbzHcZ7ocgFVo7WhkyJ4dg9llA5zXaCdHjPWnHdHRmE3w0MRvjpLnRDma39UNydUalL-V3h-fkSSdtxBfH-4x8e3-1urzOl18WHy4vlrkqC4C8gFZ3NS0UNo3qal40UjJARFV3Wm60UkWtqwYTJ1PNSuTANlQxpqpOKV6ckTez71ZasQvGyXAQXhpxfbEUk5a2U5Ylr-9oYl_P7C74n2NahnAmTkPLHv0YBW1rBlC0CXw7g9M0MWD34ExBTNmIKRtxn02CXx1dx41D_Q89hpEAOgO_jMXDf6zEx6tPq7-m-dxj4oD7hx4Zfoi0JF6J758XgjUNX6zXX8Wi-APgpK0e</recordid><startdate>200702</startdate><enddate>200702</enddate><creator>Pena, Ana-Maria</creator><creator>Fabre, Aurélie</creator><creator>Débarre, Delphine</creator><creator>Marchal-Somme, Joëlle</creator><creator>Crestani, Bruno</creator><creator>Martin, Jean-Louis</creator><creator>Beaurepaire, Emmanuel</creator><creator>Schanne-Klein, Marie-Claire</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</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>1XC</scope><orcidid>https://orcid.org/0000-0002-0513-6172</orcidid><orcidid>https://orcid.org/0000-0002-2082-8214</orcidid><orcidid>https://orcid.org/0000-0003-3026-8932</orcidid></search><sort><creationdate>200702</creationdate><title>Three-dimensional investigation and scoring of extracellular matrix remodeling during lung fibrosis using multiphoton microscopy</title><author>Pena, Ana-Maria ; Fabre, Aurélie ; Débarre, Delphine ; Marchal-Somme, Joëlle ; Crestani, Bruno ; Martin, Jean-Louis ; Beaurepaire, Emmanuel ; Schanne-Klein, Marie-Claire</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4300-309df613ce88cf6738aa20eeec6fdabdcc36d58e309adab24e702b1c22c5fcc73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Bleomycin</topic><topic>collagen</topic><topic>Collagen - ultrastructure</topic><topic>Extracellular Matrix - ultrastructure</topic><topic>Humans</topic><topic>Lung - pathology</topic><topic>lung morphology</topic><topic>Macrophages, Alveolar - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microscopy, Fluorescence, Multiphoton - methods</topic><topic>Pleura - pathology</topic><topic>Pulmonary Fibrosis - chemically induced</topic><topic>Pulmonary Fibrosis - pathology</topic><topic>second harmonic generation</topic><topic>three dimensional imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pena, Ana-Maria</creatorcontrib><creatorcontrib>Fabre, Aurélie</creatorcontrib><creatorcontrib>Débarre, Delphine</creatorcontrib><creatorcontrib>Marchal-Somme, Joëlle</creatorcontrib><creatorcontrib>Crestani, Bruno</creatorcontrib><creatorcontrib>Martin, Jean-Louis</creatorcontrib><creatorcontrib>Beaurepaire, Emmanuel</creatorcontrib><creatorcontrib>Schanne-Klein, Marie-Claire</creatorcontrib><collection>Istex</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>Hyper Article en Ligne (HAL)</collection><jtitle>Microscopy research and technique</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pena, Ana-Maria</au><au>Fabre, Aurélie</au><au>Débarre, Delphine</au><au>Marchal-Somme, Joëlle</au><au>Crestani, Bruno</au><au>Martin, Jean-Louis</au><au>Beaurepaire, Emmanuel</au><au>Schanne-Klein, Marie-Claire</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Three-dimensional investigation and scoring of extracellular matrix remodeling during lung fibrosis using multiphoton microscopy</atitle><jtitle>Microscopy research and technique</jtitle><addtitle>Microsc. 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Finally, we propose phenomenological scores of lung fibrosis and we show that they unambiguously sort out control and treated mice, with a better sensitivity and reproducibility in the subpleural region. These results should be readily generalized to other organs, as an accurate method to assess extracellular matrix remodeling during fibrosis. Microsc. Res. Tech., 2007. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17177275</pmid><doi>10.1002/jemt.20400</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0513-6172</orcidid><orcidid>https://orcid.org/0000-0002-2082-8214</orcidid><orcidid>https://orcid.org/0000-0003-3026-8932</orcidid></addata></record> |
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subjects | Animals Bleomycin collagen Collagen - ultrastructure Extracellular Matrix - ultrastructure Humans Lung - pathology lung morphology Macrophages, Alveolar - pathology Male Mice Mice, Inbred C57BL Microscopy, Fluorescence, Multiphoton - methods Pleura - pathology Pulmonary Fibrosis - chemically induced Pulmonary Fibrosis - pathology second harmonic generation three dimensional imaging |
title | Three-dimensional investigation and scoring of extracellular matrix remodeling during lung fibrosis using multiphoton microscopy |
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