TY - JOUR
T1 - Fiber-based fluorescence lifetime imaging of recellularization processes on vascular tissue constructs
AU - Alfonso-Garcia, Alba
AU - Shklover, Jeny
AU - Sherlock, Benjamin E.
AU - Panitch, Alyssa
AU - Griffiths, Leigh G.
AU - Marcu, Laura
N1 - Funding Information:
The authors would like to acknowledge the funding from the California Institute for Regenerative Medicine (CIRM) (RT3-07879) and the National Institutes of Health (NIH) (5R01HL121068-03). The authors would like to thank Dr. James Mcmasters who assisted with cell culture preparations.
Publisher Copyright:
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/9
Y1 - 2018/9
N2 - 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.
AB - 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.
KW - fiber optics imaging
KW - fluorescence lifetime imaging
KW - tissue engineering
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U2 - 10.1002/jbio.201700391
DO - 10.1002/jbio.201700391
M3 - Article
C2 - 29781171
AN - SCOPUS:85052747414
SN - 1864-063X
VL - 11
JO - Journal of Biophotonics
JF - Journal of Biophotonics
IS - 9
M1 - e201700391
ER -