Special Section on Pioneers in Biomedical Optics: Prof. Tayyaba Hasan

On the use of fluorescence probes for detecting reactive oxygen and nitrogen species associated with photodynamic therapy

[+] Author Affiliations
Michael Price

Wayne State University School of Medicine, Cancer Biology Program, Detroit, Michigan, 48201

David Kessel

Wayne State University School of Medicine, Cancer Biology Program and Department of Pharmacology, Detroit, Michigan, 48201

J. Biomed. Opt. 15(5), 051605 (September 02, 2010). doi:10.1117/1.3484258
History: Received January 17, 2010; Revised May 13, 2010; Accepted May 26, 2010; Published September 02, 2010; Online September 02, 2010
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* Address all correspondence to David Kessel, Wayne State University, Department of Pharmacology, 540 East Canfield, Detroit, Michigan, 48201, United States of America. Tel:313 577 1766, E-Mail: hkessel@med.wayne.edu

Fluorescent probes are frequently employed for the detection of different reactive oxygen and nitrogen species formed during the irradiation of photosensitized cells and tissues. Investigators often interpret the results in terms of information provided with the different probes without examining specificity or determinants of fluorogenic reactions. We examine five fluorescent probes in a cell-free system: reduced 2,7-dichlorofluorescein, dihydroethidine, dihydro-rhodamine, 3-(p aminophenyl) fluorescein (APF), and 4,5-diaminofluorescein. Of these, only APF demonstrates a high degree of specificity for a single reactive species. There is a substantial influence of peroxidase activity on all fluorogenic interactions. The fluorescence of the photosensitizing agent also must be taken into account in evaluating results.

Figures in this Article

The literature contains numerous reports on the use of fluorescent probes for detection of reactive oxygen (ROS) and nitrogen (RNS) species. Invitrogen/Molecular Probes provides a collection of such probes for which the only indication of specificity is provided by the reproduction of a table derived from Ref. 1. This compares the fluorescence of two new fluorescein analogs, APF and 3-(p-hydroxyphenyl) fluorescein (HPF), with the fluorescence of DCF in a cell-free system containing different reagents.

In the present study, we examined fluorogenic reactions associated with the exposure of five fluorogenic probes to reactive oxygen and nitrogen species, also in a cell-free system, following procedures reported in Ref. 1. The species examined were O2 [100μMKO2 in anhydrous DMSO], H2O2(100μM), and OH [formed from 20μMFe(NH4)SO4+100μMH2O2]. Fluorogenic effects of reactive nitrogen species were estimated using diethylamine nitric oxide [DEANO, 100μM]. In aqueous media, NO is released from this compound at pH 7. NO is then spontaneously oxidized to the nitrosonium cation.

Tests were carried out using 5μM concentrations of each probe in 3ml of HEPES buffer pH 7. Fluorescence was measured 30min after addition of the reagents specified above. Fluorescence excitation was provided by a 100-W quartz-halogen lamp with the wavelength selected by a monochromator. The fluorescence signal was monitored using an Instaspec IV (Oriel Corp, Stratford, Connecticut) CCD system. Excitation wavelengths were 485nm [4,5-diamino-fluorescein (DAF)], 500nm [2,7-dichlorofluorescein (DCF) and dihydroethidine (DHE)], and 490nm [dihydrorhodamine (DHR) and 3 (p-aminophenyl) fluorescein (APF)]. The fluorescence intensity at the emission optimum was recorded. All probes were obtained from Invitrogen/Molecular Probes, Eugene, Oregon, except for DEANO (Cayman Chemical Co., Ann Arbor, Michigan). Horseradish peroxide (HRP, 50μgml) was present where specified. In studies involving DHE, DNA (50μgml) was added since the long-wavelength fluorescence signal depends on binding of the oxidation product(s) to DNA.

Results are summarized in Table 1. The fluorogenic response by DCF was elicited by OHH2O2>O2, with enhanced promotion when peroxidase was present. DHE and DHR also responded to these ROS, but no substantial degree of selectivity for any ROS was observed. It has been reported that DHE can be selective for O2 detection if fluorescence (in the presence of DNA) is monitored2 at 570nm, but this probe cannot be used for an unambiguous detection of superoxide without an HPLC analysis of products.3 The presence of HRP also led to a strong promotion of probe fluorescence. HRP can promote probe oxidation by a variety of mechanisms including by direct interactions and via conversion of H2O2 to O2 and OH.45 While APF was selective for OH, especially in the presence of HPR, we have reported6 that this probe can also detect O21 to a greater extent than was suggested by Ref. 1. DAF was converted to a fluorescent product NO>OHH2O2 and O2; there was also an increase in fluorescence when HRP was present. It has been reported1 that APF can readily detect peroxinitrite ion (ONOO). The lack of response of APF to NO shown in Table 1 indicates that this species is not being produced during release of NO from the diethylamine derivative.

Table Grahic Jump Location
Probe:ROS interactions.
Table Footer NoteFluorogenic interactions between selected fluorescence probes (5μM) and reactive oxygen or nitrogen species generated as defined in the text. Numbers represent the mean fluorescence emission intensity on excitation at 490to510nm. In four replicate determinations, the variation was less than ±3% of the values shown.

While the studies reported in the table do not provide unambiguous information on fluorescence yields, i.e., fluorescence per mole of ROS or RNS, they do provide a comparison of the relative sensitivity of each probe to a given species, along with information on effects of peroxidases. In an attempt to improve specificity, Xu et al. 7 has described a naphthofluorescein derivative that emits fluorescence at 670nm on exposure to O2. It might be preferable to prepare this agent starting with 2,7-difluorofluorescein, since naphthofluoresceins are nonpolar and are difficult to work within aqueous environments. Moreover, fluorescence emission from naphthofluorescein is highly pH dependent, with a pKa of 7.5. This will complicate fluorescence measurements, especially if the probe accumulates in subcellular regions of low pH.

Maeda et al. 8 described another potentially useful probe for O2 with only a minor response to OH. This reagent is based on a nitrobenzenesulfonyl ester structure that can be cleaved by—SH reagents. This is noted in the report, but in a critical test, only a 50μM concentration was used; this is perhaps 1% of the expected intracellular GSH concentration.

These examples illustrate the problems associated with attempts to translate results obtained in cell-free systems into corresponding procedures in cell culture. Other commonly encountered problems may relate to ability of fluorescent probes to penetrate the plasma membrane, spontaneous oxidations, pH of subcellular compartments, and the presence of fluorogenic enzymes, e.g., peroxidases. We propose that if a fluorogenic ROS or RNS probe cannot clearly delineate among different reactive species in a cell-free system, using such a probe to draw conclusions concerning the appearance of such species in culture system may be unrealistic.

As a further example of difficulties in interpretation of data obtained with fluorescent probes, we reported that the Bc1-2 antagonist HA14-1 promoted the apoptotic response to photodynamic therapy9 (PDT). When a report10 appeared indicating that HA14-1 could cause the spontaneous production of ROS, we considered that the latter effect might explain, at least in part, the synergistic effect. The ability of HA14-1 to evoke formation of ROS was based on studies10 involving DCF. The fluorescence observed when HA14-1 was added to cell cultures was actually derived from a fluorogenic reaction between HA14-1 and serum albumin that mimicked11 the excitation and emission properties of DCF.

An additional consideration in the use of fluorescent probes in the context of PDT is illustrated by Fig. 1. Murine leukemia P388 cells were incubated in medium containing 2μM benzoporphyrin derivative (Verteporfin, BPD) for 60min, with a 5μM concentration of the RNS probe DAF added during the final 30min. The cells were then resuspended in fresh medium and irradiated at 690nm(90mJcm2), conditions we have found capable of killing 50% of the cell population. Fluorescence microscopy was used to assess the resulting fluorogenic interactions using 450-to490-nm excitation and monitoring fluorescence at 500 to 550 or at 500to700nm. Experimental conditions included probe alone [Figs. 1], probe+photosensitizer in the dark [Figs. 1], and after irradiation [Figs. 1].

Graphic Jump LocationF1 :

Phase contrast and fluorescence images of murine leukemia P388 cells incubated with BPD+DAF and irradiated as described in the text: (a) to (c) control cells containing only DAF, (d) to (f) cells containing DAF and BPD but not irradiated, and (g) to (i) irradiated cells loaded with DAF+BPD. Note (a), (d), and (g) are phase contrast images; (b), (e), and (h) are fluorescence images acquired at 500to700nm for 100ms; and (c), (f), and (i) are fluorescence at 500to550nm acquired for 2000ms.

Images obtained with broadband (500-to700-nm) acquisition indicated a substantial fluorogenic response when BPD was present, but this occurred whether or not the photosensitized cells were irradiated [compare Figs. 1]. The fluorescence signal appeared to derive from mitochondria, the site where BPD is localized.12 These results illustrate the fact that photosensitizing agents also fluoresce, so that care must be taken to exclude such fluorescence from the probe detection parameters. Fluorescence images obtained with narrow-band fluorescence acquisition [Figs. 1] revealed that there was no significant fluorogenic response by DAF, hence no significant formation of RNS on irradiation. The relative intensities of the fluorescence can be estimated by the time needed for image acquisition: 100ms for Figs. 1 and 2000ms for Figs. 1.

Based on studies in a cell-free system, together with additional experiments that will be reported elsewhere, we conclude that DHR can be used to distinguish H2O2 from O2, but that peroxidase activity or presence of OH can complicate interpretation of results. A prior report had arrived at a similar conclusion.13 DHE is indeed more responsive to O2 than to H2O2, but can be oxidized3 by other ROS.

Acknowledgments

This study was supported by grant CA 23378 from the NCI, NIH. Mr. Price is partially supported by GM058905-11. We thank Ann Marie Santiago for excellent technical assistance.

Setsukinai  K., , Urano  Y., , Kakinuma  K., , Majima  H. J., , and Nagano  T., “ Development of novel fluorescence probes that can reliably detect reactive oxygen species and distinguish specific species. ,” J. Biol. Chem..  0021-9258 278, , 3170–3175  ((2003)).
Zhao  H., , Kalivendi  S., , Zhang  H., , Joseph  J., , Nithipatikom  K., , Vásquez-Vivar  J., , and Kalyanaraman  B., “ Superoxide reacts with hydroethidine but forms a fluorescent product that is distinctly different from ethidium: potential implications in intracellular fluorescence detection of superoxide. ,” Free Radic Biol. Med..  0891-5849 34, , 1359–1368  ((2003)).
Zielonka  J., and Kalyanaraman  B., “ Hydroethidine- and MitoSOX-derived red fluorescence is not a reliable indicator of intracellular superoxide formation: another inconvenient truth. ,” Free Radic Biol. Med..  0891-5849 48, , 983–1001  ((2010)).
Kohler  H., and Jenzer  H., “ Interaction of lactoperoxidase with hydrogen peroxide. Formation of enzyme intermediates and generation of free radicals. ,” Free Radic Biol. Med..  0891-5849 6, , 323–339  ((1989)).
Gorris  H. H., and Walt  D. R., “ Mechanistic aspects of horseradish peroxidase elucidated through single-molecule studies. ,” J. Am. Chem. Soc..  0002-7863 131, , 6277–6782  ((2009)).
Price  M., , Reiners  J. J.  Jr., , Santiago  A. M., , and Kessel  D., “ Monitoring singlet oxygen and hydroxyl radical formation with fluorescent probes during photodynamic therapy. ,” Photochem. Photobiol..  0031-8655 85, , 1177–1181  ((2009)).
Xu  K., , Liu  X., , and Tang  B., “ Phosphinate-based red fluorescent probe for imaging the superoxide radical anion generated by RAW264.7 macrophages. ,” ChemBioChem.  1439-4227 8, , 453–458  ((2007)).
Maeda  H., , Yamamoto  K., , Kohno  I., , Hafsi  L., , Itoh  N., , Nakagawa  S., , Kanagawa  N., , Suzuki  K., , and Uno  T., “ Design of a practical fluorescent probe superoxide based on protection-deprotection chemistry of fluoresceine with benzenesulfonyl protecting groups. ,” Chemistry (Weinheim, Ger.).  0947-6539 13, , 1946–1954  ((2007)).
Kessel  D., “ Promotion of PDT efficacy by a Bcl-2 antagonist. ,” Photochem. Photobiol..  0031-8655 84, , 809–814  ((2008)).
Doshi  J. M., , Tian  D., , and Xing  C., “ Ethyl-2-amino-6-bromo-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate (HA 14-1), a prototype small-molecule antagonist against antiapoptotic Bcl-2 proteins, decomposes to generate reactive oxygen species that induce apoptosis. ,” Mol. Pharmaceut.. 4, , 919–928  ((2007)).
Kessel  D., , Price  M., , and Reiners  J. J.  Jr., “ The Bcl-2 antagonist HA14-1 forms a fluorescent albumin complex that can be mistaken for several oxidized ROS probes. ,” Photochem. Photobiol..  0031-8655 84, , 1272–1276  ((2008)).
Peng  T. I., , Chang  C. J., , Guo  M. J., , Wang  Y. H., , Yu  J. S., , Wu  H. Y., , and Jou  M. J., “ Mitochondrion-targeted photosensitizer enhances the photodynamic effect-induced mitochondrial dysfunction and apoptosis. ,” Ann. N.Y. Acad. Sci..  0077-8923 1042, , 419–428  ((2005)).
Henderson  L. M., and Chappell  J. B., “ Dihydrorhodamine 123: a fluorescent probe for superoxide generation?. ” Eur. J. Biochem..  0014-2956 217, , 973–980  ((1993)).
© 2010 Society of Photo-Optical Instrumentation Engineers

Citation

Michael Price and David Kessel
"On the use of fluorescence probes for detecting reactive oxygen and nitrogen species associated with photodynamic therapy", J. Biomed. Opt. 15(5), 051605 (September 02, 2010). ; http://dx.doi.org/10.1117/1.3484258


Figures

Graphic Jump LocationF1 :

Phase contrast and fluorescence images of murine leukemia P388 cells incubated with BPD+DAF and irradiated as described in the text: (a) to (c) control cells containing only DAF, (d) to (f) cells containing DAF and BPD but not irradiated, and (g) to (i) irradiated cells loaded with DAF+BPD. Note (a), (d), and (g) are phase contrast images; (b), (e), and (h) are fluorescence images acquired at 500to700nm for 100ms; and (c), (f), and (i) are fluorescence at 500to550nm acquired for 2000ms.

Tables

Table Grahic Jump Location
Probe:ROS interactions.
Table Footer NoteFluorogenic interactions between selected fluorescence probes (5μM) and reactive oxygen or nitrogen species generated as defined in the text. Numbers represent the mean fluorescence emission intensity on excitation at 490to510nm. In four replicate determinations, the variation was less than ±3% of the values shown.

References

Setsukinai  K., , Urano  Y., , Kakinuma  K., , Majima  H. J., , and Nagano  T., “ Development of novel fluorescence probes that can reliably detect reactive oxygen species and distinguish specific species. ,” J. Biol. Chem..  0021-9258 278, , 3170–3175  ((2003)).
Zhao  H., , Kalivendi  S., , Zhang  H., , Joseph  J., , Nithipatikom  K., , Vásquez-Vivar  J., , and Kalyanaraman  B., “ Superoxide reacts with hydroethidine but forms a fluorescent product that is distinctly different from ethidium: potential implications in intracellular fluorescence detection of superoxide. ,” Free Radic Biol. Med..  0891-5849 34, , 1359–1368  ((2003)).
Zielonka  J., and Kalyanaraman  B., “ Hydroethidine- and MitoSOX-derived red fluorescence is not a reliable indicator of intracellular superoxide formation: another inconvenient truth. ,” Free Radic Biol. Med..  0891-5849 48, , 983–1001  ((2010)).
Kohler  H., and Jenzer  H., “ Interaction of lactoperoxidase with hydrogen peroxide. Formation of enzyme intermediates and generation of free radicals. ,” Free Radic Biol. Med..  0891-5849 6, , 323–339  ((1989)).
Gorris  H. H., and Walt  D. R., “ Mechanistic aspects of horseradish peroxidase elucidated through single-molecule studies. ,” J. Am. Chem. Soc..  0002-7863 131, , 6277–6782  ((2009)).
Price  M., , Reiners  J. J.  Jr., , Santiago  A. M., , and Kessel  D., “ Monitoring singlet oxygen and hydroxyl radical formation with fluorescent probes during photodynamic therapy. ,” Photochem. Photobiol..  0031-8655 85, , 1177–1181  ((2009)).
Xu  K., , Liu  X., , and Tang  B., “ Phosphinate-based red fluorescent probe for imaging the superoxide radical anion generated by RAW264.7 macrophages. ,” ChemBioChem.  1439-4227 8, , 453–458  ((2007)).
Maeda  H., , Yamamoto  K., , Kohno  I., , Hafsi  L., , Itoh  N., , Nakagawa  S., , Kanagawa  N., , Suzuki  K., , and Uno  T., “ Design of a practical fluorescent probe superoxide based on protection-deprotection chemistry of fluoresceine with benzenesulfonyl protecting groups. ,” Chemistry (Weinheim, Ger.).  0947-6539 13, , 1946–1954  ((2007)).
Kessel  D., “ Promotion of PDT efficacy by a Bcl-2 antagonist. ,” Photochem. Photobiol..  0031-8655 84, , 809–814  ((2008)).
Doshi  J. M., , Tian  D., , and Xing  C., “ Ethyl-2-amino-6-bromo-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate (HA 14-1), a prototype small-molecule antagonist against antiapoptotic Bcl-2 proteins, decomposes to generate reactive oxygen species that induce apoptosis. ,” Mol. Pharmaceut.. 4, , 919–928  ((2007)).
Kessel  D., , Price  M., , and Reiners  J. J.  Jr., “ The Bcl-2 antagonist HA14-1 forms a fluorescent albumin complex that can be mistaken for several oxidized ROS probes. ,” Photochem. Photobiol..  0031-8655 84, , 1272–1276  ((2008)).
Peng  T. I., , Chang  C. J., , Guo  M. J., , Wang  Y. H., , Yu  J. S., , Wu  H. Y., , and Jou  M. J., “ Mitochondrion-targeted photosensitizer enhances the photodynamic effect-induced mitochondrial dysfunction and apoptosis. ,” Ann. N.Y. Acad. Sci..  0077-8923 1042, , 419–428  ((2005)).
Henderson  L. M., and Chappell  J. B., “ Dihydrorhodamine 123: a fluorescent probe for superoxide generation?. ” Eur. J. Biochem..  0014-2956 217, , 973–980  ((1993)).

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