Document Detail


Non-invasive dynamic near-infrared imaging and quantification of vascular leakage in vivo.
MedLine Citation:
PMID:  23325334     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Preclinical vascular research has been hindered by a lack of methods that can sensitively image and quantify vascular perfusion and leakage in vivo. In this study, we have developed dynamic near-infrared imaging methods to repeatedly visualize and quantify vascular leakage in mouse skin in vivo, and we have applied these methods to transgenic mice with overexpression of vascular endothelial growth factors VEGF-A or -C. Near-infrared dye conjugates were developed to identify a suitable vascular tracer that had a prolonged circulation lifetime and slow leakage into normal tissue after intravenous injection. Dynamic simultaneous imaging of ear skin and a large blood vessel in the leg enabled determination of the intravascular signal (blood volume fraction) from the tissue signal shortly after injection and quantifications of vascular leakage into the extravascular tissue over time. This method allowed for the sensitive detection of increased blood vascularity and leakage rates in K14-VEGF-A transgenic mice and also reliably measured inflammation-induced changes of vascularity and leakage over time in the same mice. Measurements after injection of recombinant VEGF-A surprisingly revealed increased blood vascular leakage and lymphatic clearance in K14-VEGF-C transgenic mice which have an expanded cutaneous lymphatic vessel network, potentially indicating unanticipated effects of lymphatic drainage on vascular leakage. Increased vascular leakage was also detected in subcutaneous tumors, confirming that the method can also be applied to deeper tissues. This new imaging method might facilitate longitudinal investigations of the in vivo effects of drug candidates, including angiogenesis inhibitors, in preclinical disease models.
Authors:
Steven T Proulx; Paola Luciani; Annamari Alitalo; Viviane Mumprecht; Ailsa J Christiansen; Reto Huggenberger; Jean-Christophe Leroux; Michael Detmar
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2013-01-17
Journal Detail:
Title:  Angiogenesis     Volume:  16     ISSN:  1573-7209     ISO Abbreviation:  Angiogenesis     Publication Date:  2013 Jul 
Date Detail:
Created Date:  2013-06-14     Completed Date:  2013-11-05     Revised Date:  2014-07-02    
Medline Journal Info:
Nlm Unique ID:  9814575     Medline TA:  Angiogenesis     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  525-40     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Analysis of Variance
Animals
Capillary Leak Syndrome / diagnosis*,  pathology*
Capillary Permeability / physiology
Cell Line, Tumor
Chromatography, High Pressure Liquid
Diagnostic Imaging / methods*
Dimethyl Sulfoxide
Female
Indoles / diagnostic use,  pharmacokinetics
Infrared Rays / diagnostic use*
Lymphatic Vessels / pathology
Mice
Mice, Inbred BALB C
Mice, Transgenic
Polyethylene Glycols
Skin / pathology*
Spectrophotometry, Ultraviolet
Vascular Endothelial Growth Factor A / genetics,  metabolism
Vascular Endothelial Growth Factor C / genetics,  metabolism
Grant Support
ID/Acronym/Agency:
CA69184/CA/NCI NIH HHS; R01 CA069184/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/IRDye800; 0/Indoles; 0/Polyethylene Glycols; 0/Vascular Endothelial Growth Factor A; 0/Vascular Endothelial Growth Factor C; 9004-74-4/monomethoxypolyethylene glycol; YOW8V9698H/Dimethyl Sulfoxide
Comments/Corrections

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


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