Fiber‐based fluorescence lifetime imaging of recellularization processes on vascular tissue constructs

• Published in: Journal of biophotonics Vol. 11; no. 9; pp. e201700391 - n/a
• Main Authors: Alfonso‐Garcia, Alba, Shklover, Jeny, Sherlock, Benjamin E., Panitch, Alyssa, Griffiths, Leigh G., Marcu, Laura
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY‐VCH Verlag GmbH & Co. KGaA 01.09.2018; Wiley Subscription Services, Inc
• Subjects: Animals; Antigens; Biomaterials; Biomedical materials; Cattle; Cell culture; Endothelial cells; Endothelial Cells - cytology; Extracellular matrix; Extracellular Matrix - metabolism; fiber optics imaging; Fluorescence; fluorescence lifetime imaging; Humans; Imaging; Maturation; Mesenchyme; Nondestructive testing; Optical Fibers; Optical Imaging - instrumentation; Pericardium; Pericardium - cytology; Scaffolds; Stem cells; Tissue Engineering; Vascular tissue; fiber optics imaging; tissue engineering; fluorescence lifetime imaging
• ISSN: 1864-063X; 1864-0648; 1864-0648
• DOI: 10.1002/jbio.201700391

New techniques able to monitor the maturation of tissue engineered constructs over time are needed for a more efficient control of developmental parameters. Here, a label‐free fluorescence lifetime imaging (FLIm) approach implemented through a single fiber‐optic interface is reported for nondestructive in situ assessment of vascular biomaterials. Recellularization processes of antigen removed bovine pericardium scaffolds with endothelial cells and mesenchymal stem cells were evaluated on the serous and the fibrous sides of the scaffolds, 2 distinct extracellular matrix niches, over the course of a 7 day culture period. Results indicated that fluorescence lifetime successfully report cell presence resolved from extracellular matrix fluorescence. The recellularization process was more rapid on the serous side than on the fibrous side for both cell types, and endothelial cells expanded faster than mesenchymal stem cells on antigen‐removed bovine pericardium. Fiber‐based FLIm has the potential to become a nondestructive tool for the assessment of tissue maturation by allowing in situ imaging of intraluminal vascular biomaterials. Fluorescence lifetime imaging (FLIm) is a nondestructive technique useful to monitor maturation of vascular engineered constructs. When implemented through a fiber‐optic interface intravascular FLIm becomes possible. Here, antigen removed bovine pericardium, a biomaterial widely utilized clinically, is recellularized with endothelial and mesenchymal stem cells. Results indicate that fiber‐based FLIm successfully resolves cell autofluorescence from the scaffold, and it reports on the faster recellularization pace of endothelial cells.