Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (11)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Navarro-Antolin, J.
Right arrow Articles by Lamas, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Navarro-Antolin, J.
Right arrow Articles by Lamas, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nephrol Dial Transplant (2001) 16: 6-9
© 2001 European Renal Association-European Dialysis and Transplant Association

Nitrosative stress by cyclosporin A in the endothelium: studies with the NO-sensitive probe diaminofluorescein-2/diacetate using flow cytometry

Javier Navarro-Antolin and Santiago Lamas1,

Centro de Investigaciones Biológicas (CIB), Consejo Superior de Investigaciones Científicas (CSIC) and 1 Instituto Reina Sofía de Investigaciones Nefrológicas (IRSIN), Madrid, Spain

Background. We have reported previously that exposure of endothelial cells to cyclosporin A (CsA) may result in the regulation of specific genes, such as the endothelial nitric oxide synthase. In the context of endothelial toxicity, whether this represents an adaptive response to injury at the physiological level or contributes further to the generation of nitrosative stress remains to be investigated. The precise reactive species potentially produced by CsA and their capacity to modify proteins functionally are not well known.

Methods. We assessed the possibility of detecting intracellular nitric oxide (NO) by flow cytometry with the cell-permeable probe diaminofluorescein-2 diacetate (DAF-2/DA).

Results. CsA increased the intracellular 2 h accumulation of DAF-2T, the oxidized form of DAF-2/DA, in an L-NAME-sensitive process. When CsA was re-added for 2 h to bovine aortic endothelial cells previously pre-incubated with CsA for 16 h, an additional increase in the accumulation of DAF-2T was achieved.

Conclusions. In this work, we provide data showing that intracellular NO can be detected by flow cytometry with DAF-2/DA and suggesting two potential mechanisms (transcriptional and post-translational) for the intracellular accumulation of NO in vascular endothelial cells exposed to the immunosuppressant CsA.

Keywords: cyclosporin A; DAF-2/DA; endothelium; flow cytometry; nitric oxide; nitrosative stress

Correspondence and offprint requests to: Santiago Lamas, Centro de Investigaciones Biológicas, c/Velázquez 144, 28006 Madrid, Spain.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
HypertensionHome page
M. Vetter, Z.-J. Chen, G.-D. Chang, D. Che, S. Liu, and C.-H. Chang
Cyclosporin A Disrupts Bradykinin Signaling Through Superoxide
Hypertension, May 1, 2003; 41(5): 1136 - 1142.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
F.-X. Yi, A. Y. Zhang, W. B. Campbell, A.-P. Zou, C. van Breemen, and P.-L. Li
Simultaneous in situ monitoring of intracellular Ca2+ and NO in endothelium of coronary arteries
Am J Physiol Heart Circ Physiol, December 1, 2002; 283(6): H2725 - H2732.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.