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A New Version of Comet Assay
DOI: 10.17691/stm2016.8.1.03 Received Jule 13, 2015
IA Chernigina, Head of Molecular Biology Laboratory, Department of Biology; T.G. Shcherbatyuk, DSc, Professor, Head of Biology Department
Nizhny Novgorod State Medical Academy, 10/1 Minin and Pozharsky Square, Nizhny Novgorod, 603005, Russian Federation
The aim of the investigation was to assess the availability of ozone to induce DNA damage in individual cells when analyzing them using the Comet assay.
Materials and Methods. Experimental studies were performed on whole blood leukocytes of white non-linear intact male rats (n=16) weighing 250±25 g. Two series of experiments were made to induce DNA damage in leukocytes. During the first series the samples were exposed to gamma-radiation, and during the second series the slides were treated with ozonized phosphate buffer saline. Further the cells were exposed to cytolysis followed by DNA denaturation, electrophoresis, neutralization, DNA being stained with a SYBR GREEN I. Comet visualization (fluorescent microscopy) and scoring were performed.
Results. The new version of the Comet assay was developed. Ozone concentration, 900 pg/L, in ozone-oxygen mixture, and the exposure time for 10 min on the cells on a microscope slides were found to be optimal for detection of Dna damage and its analysis. In addition, ozone application enables to minimize the drawbacks and limitations of gamma-radiation source.
Key words: Comet assay; DNA leukocyte damage; ozone; gamma-radiation.
The Comet assay enables to determine the level of DNA damage and repair in single, non-dividing nucleated cells. The technique was first developed by Ostling and Johansson, Swedish researchers, in 1984 [1, 2]. Currently, thousands of researches are devoted to the method applied in basic studies, and just dozens of them concern its usage in clinical medicine [1, 3-26] (Figure 1).
There are some reports informing an increased damage level of DNA in peripheral blood leukocytes is found in such diseases as coronary heart disease, diabetes mellitus (type 2), obesity and malignancies [22-26].
There are data reported on determining the basal level of DNA damage in peripheral blood lymphocytes in breast cancer and oropharyngeal cancer, and a variety of solid tumors after radiation, chemotherapy, chemoradiation and after surgical removal of the tumor by mastectomy and quadrantectomy [27-30]. The studies have demonstrated the high level of DNA damage, which the authors consider to be a serious risk factor of cancer recurrence.
Taube et al. [31] in their literature review concerned with the criteria of a new method used for cancer detection maintain that any new diagnostic technique must pass three main tests before it is approved for routine usage in clinical practice. Firstly, it must be well established and reproducible; secondly, the clinical applicability of a technique must be proved (i.e. with
For contacts: Tatiana G. Shcherbatyuk, e-mail: [email protected]
the use of this method a correct diagnosis is should be made resulting in patient’s health improvement); and, thirdly, the medical community must be convinced in the necessity for the technique use and the advantages it exhibits.
According to European scientists [32, 33], the Comet assay due to its availability can be used in clinical practice: 50-100 single nucleated cells are sufficient to analyze the DNA damage and repair. Moreover, and not least, the technique is actually an instant diagnostic test: the test results can be obtained within a few hours. However, despite the advantages, the Comet assay nowadays is still not used as a standard analytical approach in clinical laboratories. And one of the reasons is the presence of some technical difficulties, which prevent from well within-assay reproducibility [32, 33].
Currently, researchers induce DNA damage in individual cells on slides by X-ray and gamma-radiation [1, 4, 34-37]. To provide the approach, a number of technical requirements should be satisfied; the requirements limiting a wide applicability of the Comet assay in practical medicine [38].
In a special issue of Oxford journal “Mutagenesis” Andrew R. Collins, Professor of Norwegian University of Fundamental Medicine, calls for scientists to report the data on the development and updating the technique, and its application in relatively new or unstudied fields of researches [39].
20 СТМ J 2016 — vol. 8, No.1 I.A. Chernigina, T.G. Shcherbatyuk
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Figure 1. The main directions of the application of Comet assay in biomedical research
The abovementioned determines the relevance of the search of a new method modification to induce DNA damages in individual cells using the Comet assay.
The aim of the investigation was to assess the availability of ozone to induce DNA damage in individual cells to analyze them using the Comet assay.
Materials and Methods. Experimental studies were performed on whole blood leukocytes of 16 white nonlinear intact male rats weighing 250±25 g.
The work was performed in accordance with ethical principles established by European Convention for the Protection of Vertebrata used for Experimental and other Scientific Purposes (the Convention was passed in Strasburg, March, 18, 1986, adopted in Strasburg, June, 15, 2006) and approved by Ethics Committee of Nizhny Novgorod State Medical Academy.
The blood (20 ^l) was drawn via sublingual vein and mixed with 500 ^l of 0.5% low-melt-point agarose. Final leukocyte concentration in the solution was 500,000 cells/ ml. Such hemodilution is optimal for the comets under study to be equally spaced in field of vision on the slide. Further, the slides with individual cells in agarose gel we prepared. The slide was applied by the layer of 1% high-melting agarose, and dried at room temperature for better adhesion of the following layers applied [9, 40]. The suspension of cells mixed with 500 ^l of 0.5% low-melt-point agarose was applied onto solidified layer of 1% high-melting agarose (2 drops per the glass), and covered with cover slips, 24x24 mm in size. Thus, on each glass there were 2 slides with immobilized cells in
the agarose layer. Then, after the solidification of slides for 4-5 min at room temperature, the cover slips were removed for further manipulations with the cells in the agarose layer.
Two series of experiments were carried out according to the original scheme shown in Figure 2 for the induction of DNA damage in leukocytes on the slides.
The main procedures of slide treatment: lysis of cells in agarose gel composition (1 h), DNA denaturation, electrophoresis (pH>13), neutralization, and DNA staining with a SYBR GREEN I were carried out as described in the paper [4]. After staining the images of comets were photographed, mainly, in the central part of the slides, where the comets were arranged in the same plane.
The photographs were taken with a digital camera model DS series DS-Fi2 (Nikon Corporation, Japan) connected to a direct microscope Nikon Eclipse Ni-U (Nikon Corporation, Japan). The received images were processed with specialized software Comet.exe developed by Stepanov for recording and analyzing displays [41]. The 68 slides on 34 glasses were prepared in experiment totally. The 100 comets from glass have been analyzed, and average value for each experimental point was calculated. For DNA damage degree assessment we used the parameter of %TDNA, the percentage of DNA in the tail of the comet [1]. Unexposed cells served as control. The data were analyzed using software packages of Microsoft Excel 2010 and AtteStat.
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Preparation of slide
Exposure
Agarose layers:
1 — a dried layer;
2 — high-melting agarose;
3 — low-melt-point
agarose
Gamma-radiation 60Со Doses: 0.5, 1 and 3 Gy Dose rate: 1.47 Gy/min Device TERABALT 80/ACS
Microscope glass
Microscope glass
1 The concentration of ozone in the ozone-oxygen mixture leaving the ozonator for each exposure
200 |jg/L 400 |jg/L 900 |jg/L
The exposure time of OPBS to the cells in the slides —
5 and 10 min
Lysis
Alkaline
unwinding
The time of PBS bubbling with ozone — 5 min, 50 ml
Electrophoresis
Staining
Comet
visualization
Figure 2. The scheme of induction of DNA damage in leukocytes on the slides at one of the stages of the Comet assay. PBS: phosphate buffer saline; OPBS: ozonized PBS
Results and Discussion. The exposure of ionizing radiation to cells is known to be divided into direct and indirect. In the first instance, radiation interacts directly with the cell components particularly DNA and its damage disrupts the normal functioning of the cell or causes its death. In case of the indirect effect, the radiation interacts with water molecules, which constitute about 80% of the cell that leads to its radiation the radiolysis of water. This process results in the formation of free radicals particularly the highly reactive hydroxyl radical ОН that has some strong cytotoxic activity [42, 43].
Ozone reacts with the double bonds of the nitrogenous bases of nucleic acids, forming ozonides that ultimately lead to the formation of single- or doublestrand breaks in spirals [44, 45]. In water solution, the spontaneous decomposition of ozone and its reaction with the hydroxyl ions ОН- which is formed in the water due to the dissociation of some part of its molecules. Hydroxyl ion easily and quickly reacts with ozone following rather complex multi-step mechanism with the
formation of free radicals ОН and ОН/ [46]. ОН radicals in turn react with deoxyribose, being part of the nucleic acids, and this interaction underlies the mutagenic activity of hydroxyl radicals. Besides, hydroxyl radicals react with purine and pyrimidine bases of nucleic acids. It can lead to disruption of complementary bases in the DNA chain and ultimately cause cell mutation or death [44].
Thus, the mechanism of action of the ionizing radiation and ozone on cell DNA is similar: in both cases there is an oxidative stress providing some excessive production of the hydroxyl radical ОН\
The features in the morphology of comets are detected after the exposure causing DNA damage.
The nucleoids of unexposed cells have spherical form with a luminous “halo” around the core part. “Halo” is DNA loops attached to the proteins of nuclear matrix [47] (Figure 3). The comets obtained after exposure to ozone in the ozone-oxygen mixture at the concentration 900 pg/L for 5 min on the cells in the slides had short tail containing some different DNA fragments (Figure 4).
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Figure 3. The photomicrograph of the cell nucleoid without exposure (%TDNA=0.9); x200
Figure 4. The photomicrograph of the cell nucleoid after exposure with ozone 900 pg/L for 5 min (%TDNA=4.6); x200. The arrow indicates the comet head, and the tail length is marked by a curly bracket
Figure 5. The photomicrograph of the cell nucleoid after exposure with ozone 900 pg/L for 10 min (%TDNA=12.6); x200. The arrow indicates the comet head, and the tail length is marked by a curly bracket
Figure 6. The photomicrograph of the cell nucleoid after exposure with gamma-radiation at the dosage 3 Gy (%TDNA=12.4); x200
The cell nucleoids after exposure with ozone at the same concentration, 900 pg/L, but for 10 min, had the well-defined long tail (Figure 5). The Figures 3 and 4 are processed using the function Auto built in the microscope. It allows adjusting the brightness of the image to provide the best color reproduction object.
The comparison of photomicrographs of nucleoids of cells obtained after the effect (See Figure 5) and gamma-radiation at a dose of 3 Gy (Figure 6) showed Comet assay to have similar long and well-defined tails in both methods of induced DNA damage.
The analysis of the distribution of sample data according to Kolmogorov-Smirnov criterion showed the absence of differences of a normal distribution. Therefore, parametric Student t-test with Bonferonni correction for multiple comparisons were used later. The analysis of the results of the investigations didn’t reveal any significant differences of average values of the level induced DNA damage in whole blood leukocytes after exposure with ozone at various concentrations in ozone-oxygen mixture: 200, 400 and 900 pg/L for 5 min (Figure 7). However, the level of induced DNA damage in blood leukocytes after exposure with ozone at the concentration of 900 pg/L for 10 min was significantly higher than the DNA damage resulted from ozone exposure at all three concentrations for 5 min, and at the concentrations of 200 and 400 pg/L for 10 min.
The comparison of mean levels of induced DNA damage in whole blood leukocytes after exposure with ozone in ozone-oxygen mixture at the concentration of 900 pg/L for 10 min (%TDNA=12.4±1.3) and after the action of gamma-radiation 60Co at the dosage 3 Gy (%TDNA 12.5±0.4), were not detected significant differences (Figure 8).
Thus, the substitution of gamma-radiation for ozonation to detect DNA damage and repair helps to remove methodological difficulties restricting a wide use of the Comet assay in practical medicine.
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%TDNA 16.0-
14.0
12.0 10.0
8.0-1
6.0
4.0
2.0 0.0
3.6 3.5
3.7
Unexposed cells
4.3
5.6
5.5
Exposure for 5 min
2.6
3.1
12.4
Exposure for 10 min
□ Ozone concentration, 200 pg/L; и Ozone concentration, 400 pg/L; я Ozone concentration, 900 pg/L
Figure 7. The dependence of the average value of the level induced DNA damage in leukocytes of whole blood of rats on the exposure time with different concentrations of ozone in the ozone-oxygen mixture to the cells in the slides
%TDNA 14.0 "I
12.0
10.0
8.0
6.0
4.0
2.0 0.0
12.4
I '
3.7
------------------1-----" ----------
Unexposed cells Ozone,900pg/L for10min
I
12.5
Gamma-radiation, 3 Gy
Figure 8. The average value of the level induced DNA damage in leukocytes of whole blood cells after exposure with ozone at the concentrations of 900 pg/L for 10 min and gamma-radiation at the dosage of 3 Gy to the cells in the slides
Conclusion. A new version of the Comet assay technique has been developed. The effect of ozone on cells on slides, when ozone concentration in ozone-oxygen mixture is 900 pg/L and exposure time is 10 min, seems to be an optimal to apply the technique to detect and study DNA damage. The proposed approach enables us to avoid the drawbacks of traditional gamma-radiation usage.
Acknowledgements. The authors thank to the researchers of the Institute of Theoretical and Experimental Biophysics, Russian Academy of Science (Pushchino, Moscow region): Nikolay P. Sirota, the Senior Researcher, and Elena A. Kuznetsova, PhD, for helping in developing
the Comet assay, and important instructions; and Alexey A. Radaev, PhD, the Researcher of Lobachevsky State University of Nizhni Novgorod for consulting on the statistical processing of the results of research.
Study Funding and Conflicts of Interest. The study was not funded by any sources, and the authors have no conflicts of interest related to the present study.
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