Ankush Prasad
Pavel Pospíšil
Mika Tada- 1Department of Biophysics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Olomouc, Czechia
- 2Center for General Education, Tohoku Institute of Technology, Sendai, Japan
- 3Biomedical Engineering Research Laboratory, Tohoku Institute of Technology, Sendai, Japan
Editorial on the Research Topic
Reactive Oxygen Species (ROS) Detection Methods in Biological System
Metabolic processes such as respiration and oxidative stress are associated with the formation of reactive oxygen species (ROS). Any kind of fluctuation in environmental stress factors either biotic or abiotic is known to be linked with an increased level of ROS among which superoxide radical anion (O2•−); hydrogen peroxide (H2O2), hydroxyl radical (HO•), nitric oxide (NO), peroxynitrite (ONOO−), and singlet oxygen (1O2) have been widely studied (Kohno et al., 2008; Tada et al., 2009; Ichiishi et al., 2015; Zhang et al., 2018; Pospíšil et al., 2019). The ROS bear huge impact influencing the different cellular functions due to its involvement in the regulation of several cellular processes within a living system. However, because of its high reactivity, it is at the same time, harmful to the cell and is well-known to be associated with several biological dysfunction and diseases. Due to short life time and high reactivity, the detection of ROS in the biological system has always been very challenging. Different detection techniques and methodologies have been applied for quantification and localization of ROS and their reactive intermediates during the past decades both in in vitro and in vivo systems (Kohno et al., 2008; Tada et al., 2009; Ichiishi et al., 2015; Mattila et al., 2015). The detection is mainly based on:
• spectroscopic methods for instance, the use of specific spin traps and probes forming paramagnetic adducts.
• fluorescent-dependent methods where oxidant sensitive probes provide enhanced fluorescence under the condition of oxidative stress generation.
• chemiluminescent probes where monitoring of photon generation is monitored as a result of probes reaction with reactive species.
• spectrophotometric methods where reaction of reactive species with redox substances lead to change in absorbance.
• chromatographic method where separation and identification of reactive species and product are achieved.
• electrochemical sensors (such as chip-type biosensors) which is based on changes in oxidation/reduction current upon reactive species generation (Prasad et al., 2016).
The current Research Topic is aimed to bring contributions to the application of different methods for detection and localization of ROS and their reactive intermediates. We invited researchers who work on the cellular, systemic and molecular aspect of ROS to bring a group of experimental contributions on the application of different spectroscopic, microscopic and biochemical methods for the detection of reactive intermediates.
Three research articles show new findings and underscore the sophistication of the plant responses and its detection under environmental stimuli. In the study by Kumar et al., generation of ROS and subsequent protein radical formation in plants as a response to photooxidative stress has been demonstrated using electron paramagnetic resonance (EPR) spectroscopy, validated further using confocal laser scanning microscopy (CLSM), respectively. Furthermore, the characterization of protein radical was done using immuno-spin trapping. The use of immuno-spin trapping for protein radical detection is among the first of its type and can bring a new perspective toward understanding the role of protein radical for survival during photooxidative stress. Usage of fluorescent probes suffers limitations. Sedlárová and Luhová have attempted to provide a comprehensive protocol on working with CLSM and the precaution which should be taken into account while working with fluorescent probes. The authors have discussed the biological characteristics which should be taken into account as it can influence staining of samples thus providing false positive and negative results. Considering the fact that each method bears its drawback, the rational use of more than one method is recommended to conclude.
Niwano et al., discussed in the review the pro-oxidative properties of polyphenols and generation of highly reactive HO• formation as a result of its photoirradiation. The authors provide a future perspective on the usage of grape pomace which is a by-product of wine-producing as a prooxidant (such as in the manufacturing of disinfectants and other sterilizing agents). Under metal stress, level of enzymatic antioxidant system/pigments was evaluated in plants by Alam et al. in the presence of stress relief substances. The antioxidant activity was further experimentally explored and is presented in the work of Iqbal et al., where the application of polyethylene glycol (PEG) was found to reduces the oxidative stress by upregulation of the enzymatic activities of the key enzymes such as peroxidase, superoxide dismutase, ascorbate peroxidase, glutathione reductase, and catalase. In the review by McDonagh, the author dealt with post-translational modifications (PTMs) induced by ROS. The mini-review summarizes the current proteomic approaches in the identification and quantification of ROS induced PTMs and its role in cellular signaling has been reviewed.
Altogether, the articles included in this Research Topic brings exciting results on in vivo and in vitro detection and localization of ROS; the shortcoming of the detection methods and the consideration that should be taken into account; its generation from endogenous pigments; the interplay between oxidative stress and antioxidants and PTM as proteomic signatures.
Author Contributions
AP drafted the editorial. PP and MT read and modified the editorial. All authors approved it for publication.
Funding
This work was supported by the ERDF project Plants as a tool for sustainable global development (No. CZ.02.1.01/0.0/0.0/16_019/0000827) and MEXT-supported program for the strategic research foundation at private universities, Japan, S1312001, 2013.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
Ichiishi, E., Tada, M., Ohta, Y., Sami, M., Kanda, T., Ikeda, M., et al. (2015). Genomic approaches and oxygen radical measurement as biomarker candidates of off-season predictor of pollinosis: a pilot study. Curr. Pharmacogenomics Personal. Med. 13, 41–50. doi: 10.2174/187569211301151228154727
Kohno, M., Takeda, M., Niwano, Y., Saito, R., Emoto, N., Tada, M., et al. (2008). Early diagnosis of cancer by detecting the chemiluminescence of hematoporphyrins in peripheral blood lymphocytes. Tohoku J. Exp. Med. 216, 47–52. doi: 10.1620/tjem.216.47
Mattila, H., Khorobrykh, S., Havurinne, V., and Tyystjarvi, E. (2015). Reactive oxygen species: reactions and detection from photosynthetic tissues. J. Photochem. Photobiol. B 152(Pt B), 176–214. doi: 10.1016/j.jphotobiol.2015.10.001
Pospíšil, P., Prasad, A., and Rác, M. (2019). Mechanism of the formation of electronically excited species by oxidative metabolic processes: role of reactive oxygen species. Biomolecules 9:E258. doi: 10.3390/biom9070258
Prasad, A., Kikuchi, H., Inoue, K. Y., Suzuki, M., Sugiura, Y., Sugai, T., et al. (2016). Simultaneous real-time monitoring of oxygen consumption and hydrogen peroxide production in cells using our newly developed chip-type biosensor device. Front. Physiol. 7:109. doi: 10.3389/fphys.2016.00109
Tada, M., Ichiishi, E., Saito, R., Emoto, N., Niwano, Y., and Kohno, M. (2009). Myristic acid, a side chain of Phorbol Myristate Acetate (PMA), can activate human polymorphonuclear leukocytes to produce oxygen radicals more potently than PMA. J. Clin. Biochem. Nutr. 45, 309–14. doi: 10.3164/jcbn.09-30
Keywords: reactive oxygen species, oxidative stress, fluorescence imaging, proteomic signature, arsenic stress, drought
Citation: Prasad A, Pospíšil P and Tada M (2019) Editorial: Reactive Oxygen Species (ROS) Detection Methods in Biological System. Front. Physiol. 10:1316. doi: 10.3389/fphys.2019.01316
Received: 16 August 2019; Accepted: 30 September 2019;
Published: 17 October 2019.
Approved by:
Murugesan Velayutham, University of Pittsburgh, United StatesCopyright © 2019 Prasad, Pospíšil and Tada. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ankush Prasad, cHJhc2FkLmFua3VzaCYjeDAwMDQwO2dtYWlsLmNvbQ==; Pavel Pospíšil, cGF2ZWwucG9zcGlzaWwmI3gwMDA0MDt1cG9sLmN6
†ORCID: Ankush Prasad orcid.org/0000-0002-2009-8987
Pavel Pospíšil orcid.org/0000-0001-9126-2011