Non-linear imaging and characterization of atherosclerotic arterial tissue using combined SHG and FLIM microscopy
Authors: Cicchi R., Baria E., Matthäus C., Lange M., Lattermann A., Brehm BR., Popp J., Pavone FS.
Autors Affiliation: National Institute of Optics, National Research Council (INO-CNR), Largo E. Fermi 6, 50125, Florence, Italy;
European Laboratory for Non-Linear Spectroscopy (LENS), Via Nello Carrara 1, 50019, Sesto Fiorentino, Italy;
Leibniz Institute of Photonic Technology (IPHT-Jena), Albert Einstein Straße 9, 07745, Jena, Germany;
Institute of Biomedical Engineering and Nanotechnology, Ezermalas 6k, Riga, Latvia;
Institute of Pathology, Department of Neuropathology, Jena University Hospital, Friedrich Schiller University, Erlanger Allee 101, 07740 Jena, Germany;
Herz-Neuro-Zentrum Bodensee, Weinberg Strasse 1, 8280 Kreuzlingen, Switzerland,
Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich Schiller University Jena, Helmholtzweg 4, 07743 Jena, Germany;
Department of Physics, University of Florence, Via Giovanni Sansone 1, 50019, Sesto Fiorentino, Italy;
International Center of Computational Neurophotonics (ICON), Via Nello Carrara 1, 50019, Florence, Italy
Abstract: Atherosclerosis is one of the leading causes of death in the Western World and its characterization is extremely interesting from the diagnostic point of view. Here, we employed combined SHG-FLIM microscopy to characterize arterial tissue with atherosclerosis. The shorter mean fluorescence lifetime measured within plaque depositions (1260 80 ps) with respect to normal arterial wall (1480 +/- 100ps) allowed discriminating collagen from lipids. SHG measurements and image analysis demonstrated that the normal arterial wall has a more anisotropic Aspect Ratio (0.37 +/- 0.02) with respect to plaque depositions (0.61 +/- 0.02) and that the correlation length can be used for discriminating collagen fibre bundles (2.0 +/- 0.6 mu m) from cholesterol depositions (4.1 +/- 0.6 mu m). The presented method has the potential to find place in a clinical setting as well as to be applied in vivo in the near future.
Journal/Review: JOURNAL OF BIOPHOTONICS
Volume: 8 (4) Pages from: 347 to: 356
More Information: The research leading to these results has received funding from the European Union Seventh Framework Programme (FP7/2007-2013) under grant agreement number 284464, from the Italian Ministry for Education, University and Research in the framework of the Flagship Project NANOMAX, from Fondazione Pisa, from Italian Ministry of Health (GR2011-02349626), from Tuscany Region (EU-FP7-BiophotonicsPlus \”LITE\”) and from Ente Cassa di Risparmio di Firenze. Authors are grateful for support by the European network of excellence Photonics4Life (P4L).DOI: 10.1002/jbio.201400142Citations: 14data from “WEB OF SCIENCE” (of Thomson Reuters) are update at: 2019-08-18References taken from IsiWeb of Knowledge: (subscribers only)Connecting to view paper tab on IsiWeb: Click hereConnecting to view citations from IsiWeb: Click here