Abstract
The authors have developed a live-cell multimodality microscope combining epifluorescence with digital holographic microscopy; it has been implemented with a decoupling procedure allowing to separately measure from the quantitative phase important cell parameters including absolute volume, shape and integral intracellular refractive index. In combination with the numerous different specific fluorescent cellular probes, this multimodality microscopy can address important issues in cell biology. This is demonstrated by the study of intracellular calcium homeostasis associated with the change in cell volume, which play a critical role in the excitotoxicity-induced neuronal death. Comparison between quantitative phase (left) and fluorescence signal (right) on neuronal cellular bodies.
Original language | English (US) |
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Pages (from-to) | 432-436 |
Number of pages | 5 |
Journal | Journal of Biophotonics |
Volume | 3 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2010 |
Externally published | Yes |
Keywords
- Fluorescence microscopy
- Interference microscopy
- Optics and photonics
- cell biology
ASJC Scopus subject areas
- General Chemistry
- General Materials Science
- General Biochemistry, Genetics and Molecular Biology
- General Engineering
- General Physics and Astronomy