[ad_1]
Fridman, G. et al. Applied plasma medicine. Plasma Process. Polym. 5(6), 503–533 (2008).
Fridman, A. & Friedman, G. Plasma Medicine (John Wiley & Sons Inc, 2013).
Semmler, M. L. et al. Molecular mechanisms of the efficacy of cold atmospheric pressure plasma (cap) in cancer treatment. Cancers (Basel) 12(2), 269 (2020).
Alemi, P. S. et al. Synergistic effect of pressure cold atmospheric plasma and carboxymethyl chitosan to mesenchymal stem cell differentiation on PCL/CMC nanofibers for cartilage tissue engineering. Polym. Adv. Technol. 30(6), 1356–1364 (2019).
Labay, C. et al. Enhanced generation of reactive species by cold plasma in gelatin solutions for selective cancer cell death. ACS Appl. Mater. Interfaces 12(42), 47256–47269 (2020).
Mirpour, S. et al. Utilizing the micron sized non-thermal atmospheric pressure plasma inside the animal body for the tumor treatment application. Sci. Rep. 6(1), 1–10 (2016).
Volotskova, O., Dubrovsky, L., Keidar, M. & Bukrinsky, M. Cold atmospheric plasma inhibits HIV-1 replication in macrophages by targeting both the virus and the cells. PLoS ONE 11(10), e0165322 (2016).
Kaushik, N. K. et al. Plasma and nanomaterials: Fabrication and biomedical applications. Nanomaterials 9(1), 98 (2019).
Khlyustova, A., Labay, C., Machala, Z., Ginebra, M.-P. & Canal, C. Important parameters in plasma jets for the production of RONS in liquids for plasma medicine: A brief review. Front. Chem. Sci. Eng. 13(2), 238–252 (2019).
Lu, X. et al. Reactive species in non-equilibrium atmospheric-pressure plasmas: Generation, transport, and biological effects. Phys. Rep. 630, 1–84 (2016).
E. Grundmann, “Pathology, E. Rubin, JL Farber (Eds.), JB Lippincott Comp., Philadelphia (1988), 1576 pages. ISBN: 0-397-50698-8. Hard cover DM 140,-.” Urban & Fischer, 1990.
Lin, A. et al. Non-equilibrium dielectric barrier discharge treatment of mesenchymal stem cells: Charges and reactive oxygen species play the major role in cell death. Plasma Process. Polym. 12(10), 1117–1127. https://doi.org/10.1002/ppap.201400232 (2015).
Graves, D. B. The emerging role of reactive oxygen and nitrogen species in redox biology and some implications for plasma applications to medicine and biology. J. Phys. D. Appl. Phys. 45(26), 263001 (2012).
Xu, D. et al. In situ OH generation from O2− and H2O2 plays a critical role in plasma-induced cell death. PLoS ONE 10(6), e0128205 (2015).
Tobita, M., Orbay, H. & Mizuno, H. Adipose-derived stem cells: Current findings and future perspectives. Discov. Med. 11(57), 160–170 (2011).
Hass, R., Kasper, C., Böhm, S. & Jacobs, R. Different populations and sources of human mesenchymal stem cells (MSC): A comparison of adult and neonatal tissue-derived MSC. Cell Commun. Signal. 9(1), 1–14 (2011).
Yarak, S. & Okamoto, O. K. Human adipose-derived stem cells: Current challenges and clinical perspectives. An. Bras. Dermatol. 85(5), 647–656 (2010).
Bunnell, B. A., Flaat, M., Gagliardi, C., Patel, B. & Ripoll, C. Adipose-derived stem cells: Isolation, expansion and differentiation. Methods 45(2), 115–120 (2008).
Park, J. et al. Non-thermal atmospheric pressure plasma is an excellent tool to activate proliferation in various mesoderm-derived human adult stem cells. Free Radic. Biol. Med. 134, 374–384 (2019).
Miana, V. V. & González, E. A. P. Adipose tissue stem cells in regenerative medicine. Ecancermedicalscience 12, 2 (2018).
Saeedi, P., Halabian, R. & Fooladi, A. A. I. A revealing review of mesenchymal stem cells therapy, clinical perspectives and Modification strategies. Stem cell Investig. 6, 2 (2019).
Rodriguez, A.-M., Elabd, C., Amri, E.-Z., Ailhaud, G. & Dani, C. The human adipose tissue is a source of multipotent stem cells. Biochimie 87(1), 125–128 (2005).
Mizuno, H., Tobita, M. & Uysal, A. C. Concise review: adipose-derived stem cells as a novel tool for future regenerative medicine. Stem Cells 30(5), 804–810 (2012).
Rodriguez, A.-M. et al. Adipocyte differentiation of multipotent cells established from human adipose tissue. Biochem. Biophys. Res. Commun. 315(2), 255–263 (2004).
Bacou, F. et al. Transplantation of adipose tissue-derived stromal cells increases mass and functional capacity of damaged skeletal muscle. Cell Transplant. 13(2), 103–111 (2004).
Miranville, A. et al. Improvement of postnatal neovascularization by human adipose tissue-derived stem cells. Circulation 110(3), 349–355 (2004).
Planat-Benard, V. et al. Plasticity of human adipose lineage cells toward endothelial cells: Physiological and therapeutic perspectives. Circulation 109(5), 656–663 (2004).
Fathollah, S. et al. Investigation on the effects of the atmospheric pressure plasma on wound healing in diabetic rats. Sci. Rep. 6, 19144 (2016).
Mirpour, S. et al. Cold atmospheric plasma as an effective method to treat diabetic foot ulcers: A randomized clinical trial. Sci. Rep. 10(1), 1–9 (2020).
Pietkiewicz, S., Schmidt, J. H. & Lavrik, I. N. Quantification of apoptosis and necroptosis at the single cell level by a combination of imaging flow cytometry with classical annexin v/propidium iodide staining. J. Immunol. Methods 423, 99–103 (2015).
Crowley, L. C., Marfell, B. J., Scott, A. P. & Waterhouse, N. J. Quantitation of apoptosis and necrosis by annexin V binding, propidium iodide uptake, and flow cytometry. Cold Spring Harb. Protoc. 2016(11), 87288 (2016).
Babadi, M., Mohajerani, E., Ataie-Fashtami, L., Zand, N. & Shirkavand, A. Quantitative analysis of skin erythema due to laser hair removal: A diffusion optical spectroscopy analysis. J. lasers Med. Sci. 10(2), 97 (2019).
Shirkavand, A., Mohajerani, E., Farivar, S., Ataie-Fashtami, L. & Ghazimoradi, M. H. Monitoring the response of skin melanoma cell line (A375) to treatment with vemurafenib: A pilot in vitro optical spectroscopic study. Photobiomod. Photomed. Laser Surg. 39(3), 164–177 (2021).
Shirkavand, A., Farivar, S., Mohajerani, E., Ataie-Fashtami, L. & Ghazimoradi, M. H. Non-invasive reflectance spectroscopy for normal and cancerous skin cells refractive index determination: An in vitro study. Lasers Surg. Med. 51(8), 742–750 (2019).
Baskić, D., Popović, S., Ristić, P. & Arsenijević, N. N. Analysis of cycloheximide-induced apoptosis in human leukocytes: Fluorescence microscopy using annexin V/propidium iodide versus acridin orange/ethidium bromide. Cell Biol. Int. 30(11), 924–932 (2006).
Shi, X.-M. et al. Viability reduction of melanoma cells by plasma jet via inducing G1/S and G2/M cell cycle arrest and cell apoptosis. IEEE Trans. Plasma Sci. 42(6), 1640–1647 (2014).
Batsali, A. K. et al. Differential expression of cell cycle and WNT pathway-related genes accounts for differences in the growth and differentiation potential of Wharton’s jelly and bone marrow-derived mesenchymal stem cells. Stem Cell Res. Ther. 8(1), 1–17 (2017).
Kajstura, M., Halicka, H. D., Pryjma, J. & Darzynkiewicz, Z. Discontinuous fragmentation of nuclear DNA during apoptosis revealed by discrete ‘sub-G1’ peaks on DNA content histograms. Cytom. Part A J. Int. Soc. Anal. Cytol. 71(3), 125–131 (2007).
Amer, J., Goldfarb, A. & Fibach, E. Flow cytometric measurement of reactive oxygen species production by normal and thalassaemic red blood cells. Eur. J. Haematol. 70(2), 84–90 (2003).
Christov, A., Hamdheydari, L. & Grammas, P. Detection of reactive oxygen species by flow cytometry. In Methods in Biological Oxidative Stress 175–184 (Springer, 2003).
Ghaleno, L. R. et al. Evaluation of conventional semen parameters, intracellular reactive oxygen species, DNA fragmentation and dysfunction of mitochondrial membrane potential after semen preparation techniques: A flow cytometric study. Arch. Gynecol. Obstet. 289(1), 173–180 (2014).
Šimončicová, J., Kryštofová, S., Medvecká, V., Ďurišová, K. & Kaliňáková, B. Technical applications of plasma treatments: Current state and perspectives. Appl. Microbiol. Biotechnol. 103(13), 5117–5129 (2019).
Peterková, L. et al. Argon plasma-treated fluorinated ethylene propylene: Growth of primary dermal fibroblasts and mesenchymal stem cells. Tissue Cell 58, 121–129 (2019).
Zhou, H. et al. Effects of Exendin-4 on bone marrow mesenchymal stem cell proliferation, migration and apoptosis in vitro. Sci. Rep. 5(1), 1–14 (2015).
Yusupov, M. et al. Reactive molecular dynamics simulations of oxygen species in a liquid water layer of interest for plasma medicine. J. Phys. D. Appl. Phys. 47(2), 25205 (2013).
Dominici, M. et al. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy 8(4), 315–317 (2006).
Tan, F., Fang, Y., Zhu, L. & Al-Rubeai, M. Controlling stem cell fate using cold atmospheric plasma. Stem Cell Res. Ther. 11(1), 1–10 (2020).
Miletić, M. et al. Effects of non-thermal atmospheric plasma on human periodontal ligament mesenchymal stem cells. J. Phys. D. Appl. Phys. https://doi.org/10.1088/0022-3727/46/34/345401 (2013).
Girard, P.-M. et al. Synergistic effect of H2O2 and NO2 in cell death induced by cold atmospheric He plasma. Sci. Rep. 6(1), 1–17 (2016).
Szili, E. J., Hong, S.-H., Oh, J.-S., Gaur, N. & Short, R. D. Tracking the penetration of plasma reactive species in tissue models. Trends Biotechnol. 36(6), 594–602 (2018).
Halliwell, B. & Gutteridge, J. M. C. Free Radicals in Biology and Medicine (Oxford University Press, 2015).
Privat-Maldonado, A. et al. Ros from physical plasmas: Redox chemistry for biomedical therapy. Oxid. Med. Cell. Longev. 20, 19 (2019).
Ahn, H. J. et al. Atmospheric-pressure plasma jet induces apoptosis involving mitochondria via generation of free radicals. PLoS ONE 6(11), e28154 (2011).
Kalghatgi, S. et al. Effects of non-thermal plasma on mammalian cells. PLoS ONE 6(1), e16270 (2011).
Iseki, S. et al. Selective killing of ovarian cancer cells through induction of apoptosis by nonequilibrium atmospheric pressure plasma. Appl. Phys. Lett. 100(11), 113702 (2012).
Sheikh, M. S., Antinore, M. J., Huang, Y. & Fornace, A. J. Ultraviolet-irradiation-induced apoptosis is mediated via ligand independent activation of tumor necrosis factor receptor 1. Oncogene 17(20), 2555–2563 (1998).
Laurent, A. et al. Controlling tumor growth by modulating endogenous production of reactive oxygen species. Cancer Res. 65(3), 948–956 (2005).
Maraldi, T., Angeloni, C., Giannoni, E., & Sell, C. Reactive oxygen species in stem cells. Hindawi, 2015.
Chaudhari, P., Ye, Z. & Jang, Y.-Y. Roles of reactive oxygen species in the fate of stem cells. Antioxid. Redox Signal. 20(12), 1881–1890 (2014).
Kalghatgi, S., Friedman, G., Fridman, A. & Clyne, A. M. Endothelial cell proliferation is enhanced by low dose non-thermal plasma through fibroblast growth factor-2 release. Ann. Biomed. Eng. 38(3), 748–757. https://doi.org/10.1007/s10439-009-9868-x (2010).
Liou, G.-Y. & Storz, P. Reactive oxygen species in cancer. Free Radic. Res. 44(5), 479–496 (2010).
Wang, K. et al. Redox homeostasis: The linchpin in stem cell self-renewal and differentiation. Cell Death Dis. 4(3), e537–e537 (2013).
MacMicking, J., Xie, Q. & Nathan, C. Nitric oxide and macrophage function. Annu. Rev. Immunol. 15(1), 323–350 (1997).
Cheng, A., Wang, S., Cai, J., Rao, M. S. & Mattson, M. P. Nitric oxide acts in a positive feedback loop with BDNF to regulate neural progenitor cell proliferation and differentiation in the mammalian brain. Dev. Biol. 258(2), 319–333 (2003).
Brüne, B. Nitric oxide: NO apoptosis or turning it ON?. Cell Death Differ. 10(8), 864–869 (2003).
Villalobo, A. Nitric oxide and cell proliferation. FEBS J. 273(11), 2329–2344 (2006).
Bogdan, C. Nitric oxide and the immune response. Nat. Immunol. 2(10), 907–916 (2001).
Tejedo, J. R. et al. Low concentrations of nitric oxide delay the differentiation of embryonic stem cells and promote their survival. Cell Death Dis. 1(10), e80–e80 (2010).
Carreras, M. C. & Poderoso, J. J. Mitochondrial nitric oxide in the signaling of cell integrated responses. Am. J. Physiol. Physiol. 292(5), C1569–C1580 (2007).
Park, J. et al. Non-thermal atmospheric pressure plasma efficiently promotes the proliferation of adipose tissue-derived stem cells by activating NO-response pathways. Sci. Rep. 6(1), 1–12 (2016).
Park, J. et al. Non-thermal atmospheric pressure plasma induces epigenetic modifications that activate the expression of various cytokines and growth factors in human mesoderm-derived stem cells. Free Radic. Biol. Med. 148, 108–122 (2020).
[ad_2]
Source link