Back to Search
Start Over
Mechanisms and kinetic profiles of superoxide-stimulated nitrosative processes in cells using a diaminofluorescein probe.
- Source :
-
Free Radical Biology & Medicine . Dec2014, Vol. 77, p270-280. 11p. - Publication Year :
- 2014
-
Abstract
- In this study, we examined the mechanisms and kinetic profiles of intracellular nitrosative processes using diaminofluorescein (DAF-2) as a target in RAW 264.7 cells. The intracellular formation of the fluorescent, nitrosated product diaminofluorescein triazol (DAFT) from both endogenous and exogenous nitric oxide (NO ) was prevented by deoxygenation and by cell membrane-permeable superoxide (O 2 − ) scavengers but not by extracellular bovine Cu,Zn-SOD. In addition, the DAFT formation rate decreased in the presence of cell membrane-permeable Mn porphyrins that are known to scavenge peroxynitrite (ONOO − ) but was enhanced by HCO 3 − /CO 2 . Together, these results indicate that nitrosative processes in RAW 264.7 cells depend on endogenous intracellular O 2 − and are stimulated by ONOO − /CO 2 -derived radical oxidants. The N 2 O 3 scavenger sodium azide (NaN 3 ) only partially attenuated the DAFT formation rate and only with high NO (>120 nM), suggesting that DAFT formation occurs by nitrosation (azide-susceptible DAFT formation) and predominantly by oxidative nitrosylation (azide-resistant DAFT formation). Interestingly, the DAFT formation rate increased linearly with NO concentrations of up to 120–140 nM but thereafter underwent a sharp transition and became insensitive to NO . This behavior indicates the sudden exhaustion of an endogenous cell substrate that reacts rapidly with NO and induces nitrosative processes, consistent with the involvement of intracellular O 2 − . On the other hand, intracellular DAFT formation stimulated by a fixed flux of xanthine oxidase-derived extracellular O 2 − that also occurs by nitrosation and oxidative nitrosylation increased, peaked, and then decreased with increasing NO , as previously observed. Thus, our findings complementarily show that intra- and extracellular O 2 − -dependent nitrosative processes occurring by the same chemical mechanisms do not necessarily depend on NO concentration and exhibit different unusual kinetic profiles with NO dynamics, depending on the biological compartment in which NO and O 2 − interact. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 08915849
- Volume :
- 77
- Database :
- Academic Search Index
- Journal :
- Free Radical Biology & Medicine
- Publication Type :
- Academic Journal
- Accession number :
- 99829311
- Full Text :
- https://doi.org/10.1016/j.freeradbiomed.2014.09.012