Birefringence microscopy platform for assessing airway smooth muscle structure and function in vivo
The inability to visualize airway smooth muscle (ASM) cells in vivo is a major obstacle in understanding their role in normal physiology and diseases. At present, there is no imaging modality available to assess ASM in vivo. Confocal endomicroscopy lacks the penetration depth and field of view, and...
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Published in | Science translational medicine Vol. 8; no. 359; p. 359ra131 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
05.10.2016
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Subjects | |
Online Access | Get full text |
ISSN | 1946-6242 1946-6234 1946-6242 |
DOI | 10.1126/scitranslmed.aag1424 |
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Abstract | The inability to visualize airway smooth muscle (ASM) cells in vivo is a major obstacle in understanding their role in normal physiology and diseases. At present, there is no imaging modality available to assess ASM in vivo. Confocal endomicroscopy lacks the penetration depth and field of view, and conventional optical coherence tomography (OCT) does not have sufficient contrast to differentiate ASM from surrounding tissues. We have developed a birefringence microscopy platform that leverages the micro-organization of tissue to add further dimension to traditional OCT. We have used this technology to validate ASM measurements in ex vivo swine and canine studies, visualize and characterize volumetric representations of ASM in vivo, and quantify and predict ASM contractile force as a function of optical retardation. We provide in vivo images and volumetric assessments of ASM in living humans and document structural disease variations in subjects with mild asthma. The opportunity to link inflammatory responses to ASM responses and to link ASM responses to clinical responses and outcomes could lead to an increased understanding of diseases of the airway and, ultimately, to improved patient outcomes. |
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AbstractList | The inability to visualize airway smooth muscle (ASM) cells in vivo is a major obstacle in understanding their role in normal physiology and diseases. At present, there is no imaging modality available to assess ASM in vivo. Confocal endomicroscopy lacks the penetration depth and field of view, and conventional optical coherence tomography (OCT) does not have sufficient contrast to differentiate ASM from surrounding tissues. We have developed a birefringence microscopy platform that leverages the micro-organization of tissue to add further dimension to traditional OCT. We have used this technology to validate ASM measurements in ex vivo swine and canine studies, visualize and characterize volumetric representations of ASM in vivo, and quantify and predict ASM contractile force as a function of optical retardation. We provide in vivo images and volumetric assessments of ASM in living humans and document structural disease variations in subjects with mild asthma. The opportunity to link inflammatory responses to ASM responses and to link ASM responses to clinical responses and outcomes could lead to an increased understanding of diseases of the airway and, ultimately, to improved patient outcomes. |
Author | Suter, Melissa J Griffith, Jason W Hamilos, Daniel L Adams, David C Cho, Josalyn L Holz, Jasmin A Wang, Yan Hariri, Lida P Szabari, Margit V Scott Harris, R Miller, Alyssa J Luster, Andrew D Villiger, Martin Medoff, Benjamin D Bouma, Brett E |
Author_xml | – sequence: 1 givenname: David C surname: Adams fullname: Adams, David C organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 2 givenname: Lida P surname: Hariri fullname: Hariri, Lida P organization: Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 3 givenname: Alyssa J surname: Miller fullname: Miller, Alyssa J organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 4 givenname: Yan surname: Wang fullname: Wang, Yan organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 5 givenname: Josalyn L surname: Cho fullname: Cho, Josalyn L organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 6 givenname: Martin surname: Villiger fullname: Villiger, Martin organization: Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 7 givenname: Jasmin A surname: Holz fullname: Holz, Jasmin A organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 8 givenname: Margit V surname: Szabari fullname: Szabari, Margit V organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 9 givenname: Daniel L surname: Hamilos fullname: Hamilos, Daniel L organization: Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 10 givenname: R surname: Scott Harris fullname: Scott Harris, R organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 11 givenname: Jason W surname: Griffith fullname: Griffith, Jason W organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 12 givenname: Brett E surname: Bouma fullname: Bouma, Brett E organization: Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 13 givenname: Andrew D surname: Luster fullname: Luster, Andrew D organization: Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 14 givenname: Benjamin D surname: Medoff fullname: Medoff, Benjamin D organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA – sequence: 15 givenname: Melissa J surname: Suter fullname: Suter, Melissa J email: msuter@mgh.harvard.edu organization: Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. msuter@mgh.harvard.edu |
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Snippet | The inability to visualize airway smooth muscle (ASM) cells in vivo is a major obstacle in understanding their role in normal physiology and diseases. At... |
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SubjectTerms | Animals Asthma - physiopathology Birefringence Cartilage - anatomy & histology Case-Control Studies Dogs Humans Imaging, Three-Dimensional Microscopy - methods Muscle Contraction Muscle Relaxation Muscle, Smooth - anatomy & histology Muscle, Smooth - physiology Respiratory System - anatomy & histology Sus scrofa Tomography, Optical Coherence |
Title | Birefringence microscopy platform for assessing airway smooth muscle structure and function in vivo |
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