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Updated: Jun 5, 2026

Production and Multi-Parameter Live Cell Fluorescence Lifetime Imaging Microscopy (FLIM) of Multicellular Spheroids
Published on: August 9, 2024
Multiphoton fluorescence lifetime imaging of 3D-stem cell spheroids during differentiation
Karsten König1, Aisada Uchugonova, Erwin Gorjup
1Saarland University, Department of Biophotonics and Laser Technology, Faculty of Mechatronics and Physics, 66123 Saarbrücken, Germany. k.koenig@blt.uni-saarland.de
Abstract:
Long-term high-resolution multiphoton imaging of nonlabeled human salivary gland stem cell spheroids has been performed with submicron spatial resolution, 10.5-nm spectral resolution, and picosecond temporal resolution. In particular, the two-photon-excited coenzyme NAD(P)H and flavins have been detected by time-correlated single photon counting (TCSPC). Stem cells increased their autofluorescence lifetimes and decreased their total fluorescence intensity during the adipogenic-differentiation process. In addition, the onset of the biosynthesis of lipid vacuoles was monitored over a period of several weeks in stem-cell spheroids. Time-resolved multiphoton autofluorescence imaging microscopes may become a promising tool for marker-free stem-cell characterization and cell sorting.
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