Title | Assessment of cardiovascular fibrosis using novel fluorescent probes. |
Publication Type | Journal Article |
Year of Publication | 2011 |
Authors | Chen J, Lee SKoo, Abd-Elgaliel WR, Liang L, Galende E-Y, Hajjar RJ, Tung C-H |
Journal | PLoS One |
Volume | 6 |
Issue | 4 |
Pagination | e19097 |
Date Published | 2011 Apr 20 |
ISSN | 1932-6203 |
Keywords | Animals, Cardiovascular Diseases, Fibrosis, Fluorescent Dyes, Male, Rats, Rats, Sprague-Dawley, Staining and Labeling |
Abstract | Cardiovascular fibrosis resulted from pressure overload or ischemia could alter myocardial stiffness and lead to ventricular dysfunction. Fluorescently labeled collagen-binding protein CNA 35, derived from the surface component of Staphylococcus aureus, and a novel synthetic biphenylalanine containing peptide are applied to stain fibrosis associated collagen and myocytes, respectively. Detailed pathological characteristics of cardiovascular fibrosis could be identified clearly in 2 hours. This staining pair requires only simple staining and brief washing, generating less than 10 ml of waste. The image information collected by this novel fluorescent staining pair is compatible with it collected by the traditional Masson's Trichrome and Picrosirius Red staining which are widely used to stain cardiovascular fibrosis and isolated cells. |
DOI | 10.1371/journal.pone.0019097 |
Alternate Journal | PLoS One |
PubMed ID | 21533060 |
PubMed Central ID | PMC3080412 |
Grant List | R01 CA135312 / CA / NCI NIH HHS / United States CA135312 / CA / NCI NIH HHS / United States R01HL093183 / HL / NHLBI NIH HHS / United States R01 HL088434 / HL / NHLBI NIH HHS / United States R01HL088434 / HL / NHLBI NIH HHS / United States P20HL100396 / HL / NHLBI NIH HHS / United States P20 HL100396 / HL / NHLBI NIH HHS / United States R01 HL093183 / HL / NHLBI NIH HHS / United States |
Related Institute:
Molecular Imaging Innovations Institute (MI3)