Journal
JOURNAL OF BIOMEDICAL OPTICS
Volume 16, Issue 3, Pages -Publisher
SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS
DOI: 10.1117/1.3560513
Keywords
ATP; apoptosis; mitochondrial dysfunction; NADH fluorescence lifetime; mitochondrial membrane potential; oxygen consumption
Funding
- Ministry of Education of Taiwan [NSC94-2321-B-010-004-YC, NSC98-2112-M-010-003]
- National Science Council of Taiwan [NSC97-2320-B-010-013-MY3]
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In vivo noninvasive detection of apoptosis represents a new tool that may yield a more definite diagnosis, a more accurate prognosis, and help improve therapies for human diseases. The intrinsic fluorescence of reduced nicotinamide adenine dinucleotide (NADH) may be a potential optical bionnarker for the apoptosis detection because NADH is involved in the respiration for the mitochondrial membrane potential (Delta Psi) formation and adenosine-5'-triphosphate (ATP) synthesis, and the depletion of Delta Psi and ATP level is the hallmark of apoptosis. We have previously observed the NADH fluorescence lifetime change is associated with staurosporine (STS)-induced mitochondria-mediated apoptosis. However, its relationship with mitochondrial functions such as Delta Psi, ATP, and oxygen consumption rate is not clear. In this study, we investigated this relationship. Our results indicate that the NADH fluorescence lifetime increased when Delta Psi and ATP levels were equal to or higher than their values of controls and decreased before the depletion of Delta Psi and ATP, and the oxygen consumption rate did not change. These findings suggest that the increased NADH fluorescence lifetime in STS-induced cell death occurred before the depletion of Delta Psi and ATP and activation of caspase 3, and was not simply caused by cellular metabolic change. Furthermore, the NADH fluorescence lifetime change is associated with the pace of apoptosis. (C) 2011 Society of Photo-Optical Instrumentation Engineers (SPIE). [DOI: 10.1117/1.3560513]
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