Document Detail


Visualization of pulmonary inflammation using noninvasive fluorescence molecular imaging.
MedLine Citation:
PMID:  18202169     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The ability to visualize molecular processes and cellular regulators of complex pulmonary diseases such as asthma, chronic obstructive pulmonary disease (COPD), or adult respiratory distress syndrome (ARDS), would aid in the diagnosis, differentiation, therapy assessment and in small animal-based drug-discovery processes. Herein we report the application of normalized transillumination and fluorescence molecular tomography (FMT) for the noninvasive quantitative imaging of the mouse lung in vivo. We demonstrate the ability to visualize and quantitate pulmonary response in a murine model of LPS-induced airway inflammation. Twenty-four hours prior to imaging, BALB/c female mice were injected via tail vein with 2 nmol of a cathepsin-sensitive activatable fluorescent probe (excitation: 750 nm; emission: 780 nm) and 2 nmol of accompanying intravascular agent (excitation: 674 nm; emission: 694 nm). Six hours later, the mice were anesthetized with isoflurane and administered intranasal LPS in sterile 0.9% saline in 25 microl aliquots (one per nostril). Fluorescence molecular imaging revealed the in vivo profile of cysteine protease activation and vascular distribution within the lung typifying the inflammatory response to LPS insult. Results were correlated with standard in vitro laboratory tests (Western blot, bronchoalveolar lavage or BAL analysis, immunohistochemistry) and revealed good correlation with the underlying activity. We demonstrated the capacity of fluorescence tomography to noninvasively and longitudinally characterize physiological, cellular, and subcellular processes associated with inflammatory disease burden in the lung. The data presented herein serve to further evince fluorescence molecular imaging as a technology highly appropriate for the biomedical laboratory.
Authors:
Jodi Haller; Damon Hyde; Nikolaos Deliolanis; Ruben de Kleine; Mark Niedre; Vasilis Ntziachristos
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2008-01-17
Journal Detail:
Title:  Journal of applied physiology (Bethesda, Md. : 1985)     Volume:  104     ISSN:  8750-7587     ISO Abbreviation:  J. Appl. Physiol.     Publication Date:  2008 Mar 
Date Detail:
Created Date:  2008-03-10     Completed Date:  2008-05-23     Revised Date:  2013-09-26    
Medline Journal Info:
Nlm Unique ID:  8502536     Medline TA:  J Appl Physiol (1985)     Country:  United States    
Other Details:
Languages:  eng     Pagination:  795-802     Citation Subset:  IM    
Affiliation:
Center for Molecular Imaging Research Laboratory For Bio-optics and Molecular Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Disease Models, Animal
Female
Fluorescence*
Fluorescent Dyes / administration & dosage
Imaging, Three-Dimensional
Injections, Intravenous
Lipopolysaccharides
Lung / pathology*
Mice
Mice, Inbred BALB C
Pneumonia, Bacterial / chemically induced,  pathology*
Signal Processing, Computer-Assisted
Tomography, Optical / methods*
Grant Support
ID/Acronym/Agency:
R01-EB-00750/EB/NIBIB NIH HHS; R33-CA-91807/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Fluorescent Dyes; 0/Lipopolysaccharides; 0/lipopolysaccharide, E coli O55-B5

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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