Fluorescence quenching of free and bound NADH in HeLa cells determined by hyperspectral imaging and unmixing of cell autofluorescence

• Published in: Biomedical optics express Vol. 8; no. 3; pp. 1488 - 1498
• Main Authors: Rehman, Aziz Ul, Anwer, Ayad G, Gosnell, Martin E, Mahbub, Saabah B, Liu, Guozhen, Goldys, Ewa M
• Format: Journal Article
• Language: English
• Published: United States Optical Society of America 01.03.2017
• Subjects: (110.4234) Multispectral and hyperspectral imaging; (100.2960) Image analysis; (170.2520) Fluorescence microscopy
• ISSN: 2156-7085; 2156-7085
• DOI: 10.1364/BOE.8.001488

Carbonyl cyanide-p-trifluoro methoxyphenylhydrazone (FCCP) is a well-known mitochondrial uncoupling agent. We examined FCCP-induced fluorescence quenching of reduced nicotinamide adenine dinucleotide / nicotinamide adenine dinucleotide phosphate (NAD(P)H) in solution and in cultured HeLa cells in a wide range of FCCP concentrations from 50 to 1000µM. A non-invasive label-free method of hyperspectral imaging of cell autofluorescence combined with unsupervised unmixing was used to separately isolate the emissions of free and bound NAD(P)H from cell autofluorescence. Hyperspectral image analysis of FCCP-treated HeLa cells confirms that this agent selectively quenches fluorescence of free and bound NAD(P)H in a broad range of concentrations. This is confirmed by the measurements of average NAD/NADH and NADP/NADPH content in cells. FCCP quenching of free NAD(P)H in cells and in solution is found to be similar, but quenching of bound NAD(P)H in cells is attenuated compared to solution quenching possibly due to a contribution from the metabolic and/or antioxidant response in cells. Chemical quenching of NAD(P)H fluorescence by FCCP validates the results of unsupervised unmixing of cell autofluorescence.