Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 

 Table of Contents  
Year : 2021  |  Volume : 17  |  Issue : 2  |  Page : 537-542

In vivo study of interferon-γ, transforming growth factor-β, and interleukin-4 gene expression induced by radioadaptive response

1 Medical Physics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
2 Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
3 Department of Medical Physics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
4 Department of Radiology Technology, School of Paramedical Sciences, Mashhad University of Medical Sciences, Mashhad, Iran
5 Department of Medical Physics, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
6 Department of Medical Physics, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

Date of Submission28-Jan-2019
Date of Decision08-Jan-2020
Date of Acceptance21-Jan-2020
Date of Web Publication28-Oct-2020

Correspondence Address:
Sepideh Abdollahi-Dehkordi
Department of Medical Physics, Faculty of Medicine, Iran University of Medical Sciences, Tehran
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/jcrt.JCRT_71_19

Rights and Permissions
 > Abstract 

Introduction: In the present study, the radioadaptive role of the immune system induced by low dose (LD) was investigated for its in vivo protective activity.
Materials and Methods: Quantitative analysis of cytokine gene expression was assessed for their in vivo activity in BALB/c mice. To evaluate the adaptive response induced by LD on the mice spleen lymphocyte, the cytokine interleukin (IL)-4, interferon (IFN)-γ, and transforming growth factor (TGF)-β expression was measured by a real-time quantitative polymerase chain reaction. To verify the radioadaptive effect of LD, animals were preirradiated at 10 cGy from a 60 Co source and then challenge dose at 200 cGy was delivered. Independent sample student's t-test was employed to compare cytokine gene expression in radioadaptive (10 + 200 cGy), LD (10 cGy), high-dose (HD, 200 cGy), and control groups of animals.
Results: Following the HD, the cytokine gene expression of IFN-γ, IL-4, and TGF-β was significantly decreased compared to the control group (P = 0.0001). However, TGF-β expression was also decreased significantly in the LD and adaptive groups compared to the control group (P = 0.0001). IFN-γ/IL-4 ratio in the adaptive group was significantly decreased compared to the HD group (P = 0.0001).
Conclusion: These results indicate that the immune system plays an important role for radioadaptive response induction by LD radiation to adjust the harmful effects of HD irradiation.

Keywords: Gene expression profiling, immune system, low-dose ionizing radiation, radioadaptive response

How to cite this article:
Bahreyni-Toossi MT, Sankian M, Azimian H, Najafi-Amiri M, Khademi S, Abdollahi-Dehkordi S, Hamzian N. In vivo study of interferon-γ, transforming growth factor-β, and interleukin-4 gene expression induced by radioadaptive response. J Can Res Ther 2021;17:537-42

How to cite this URL:
Bahreyni-Toossi MT, Sankian M, Azimian H, Najafi-Amiri M, Khademi S, Abdollahi-Dehkordi S, Hamzian N. In vivo study of interferon-γ, transforming growth factor-β, and interleukin-4 gene expression induced by radioadaptive response. J Can Res Ther [serial online] 2021 [cited 2021 Nov 29];17:537-42. Available from: https://www.cancerjournal.net/text.asp?2021/17/2/537/299462

 > Introduction Top

Adaptive response (AR) is an important biological effect following low-dose (LD) ionizing radiation (IR) which for the first time was confirmed by Olivieri et al.[1] This protective phenomenon has been observed in both normal and tumor cells.[2] This is interpreted as a resistive reaction of cells to a high dose (HD) when they initially are exposed to a LD. AR was approved by studying various endpoints including DNA damage, cellular damage, micronucleus formation, chromosomal aberration, neoplasm formation, or apoptosis induction. Some studies have linked AR to the immune system, repair mechanisms, and molecular pathways.[3],[4],[5],[6] The value of LD and HD, dose rate, and the time interval between LD and HD have an effect on AR outcome.[7] Helper T-cells are possibly the most important cells in adaptive immunity, as they are required for almost all adaptive immune responses.[8],[9] T helper (Th1) cells produce interleukin (IL)-2 and interferon (IFN)-γ that organize cell-mediated immunity against intracellular pathogens and tumors.[1],[10] Th2 cells produce IL-4, IL-5, and IL-13. The two helper T-cell sessions also differ by the type of immune response they produce. While Th1 cells tend to produce responses against intracellular parasites such as bacteria and viruses, Th2 cells produce immune responses against helminths and other extracellular parasites and involving allergic reaction such as asthma and atopic dermatitis.[11],[12] Moreover, the Th1/Th2 concept suggests that modulation of the relative contribution of Th1- or Th2-type cytokines makes possible to regulate the balance between protection and immunopathology, as well as the development and/or the severity of some immunologic disorders, for example, multiple sclerosis, systemic lupus erythematosus, and rheumatoid arthritis.[8],[13],[14] Due to the sensitivity of the immune system to IR, it is a critical system that plays a functional and decisive role in the development of long-term effects, including leukemia and tumor formation.[15] Hence, several studies have investigated the effects of LD and HDIR on the immune system and the changes of gene expression levels both in vivo and in vitro.[5] Furthermore, some investigators have studied DNA damage of mouse spleen cells.[16],[17] Immune response to IR depends on many factors such as dose and dose rate.[18] Suppression of the immune system and induction of inflammatory processes are common effects of HDIR;[19] however, the effects of LD radiation on the immune system response are not clear and are a controversial issue.

The aim of this study was to investigate the impact of adaptive radiation response on the immune system in mice. For this purpose, a number of important parameters in the immune system such as gene expression of Th1, Th2, and Treg cytokines were examined.

 > Materials and Methods Top

Experimental animals and radiation

Seven-eight week-old male BALB/c mice, weighting 23–25 g, were purchased from Pasteur Institute of Iran for this study. The animals were acclimated for 2 weeks and then randomly divided into four groups. They were housed in a specific-pathogen-free environment of the laboratory. The mice were divided into four groups and were total-body irradiated to a total dose of 0, 0.1, 2, and 0.1 + 2 (Gy) by a 60 Co teletherapy unit (Theratron, Phoenix Model, Canada) at Source-Skin Distance (SSD) = 80 cm and field size = 7 × 18 cm 2. Dose rates were 449 mGy/min and 31 mGy/min for delivering HD and LD, respectively. Dosimetry was performed with a Farmer-type 0.6 cm ionization chamber and a Farmer 2581 electrometer.

Isolation of lymphocytes

Mice were killed 24 h after irradiation, and spleens were mechanically extracted; erythrocytes were lysed with 1.66% ammonium chloride solution. Cells were resuspended in RPMI-1640 culture medium supplemented with 5% Fetal Calf Serum (FCS), 10 mM Hepes, 20 mM beta-mercaptoethanol, 100 U/ml penicillin, 100 mg/ml streptomycin, and 2.5 mg/ml amphotericin B. The number of viable splenocytes was determined using a microscope with trypan blue exclusion of dead cells. Single-cell suspensions of splenocytes were used for subsequent immunological measurements.

Measuring cytokine expression of unfractionated total splenocytes by real-time reverse transcription-polymerase chain reaction

Mouse spleens were removed 24 h following irradiation. RNAs were isolated from the unfractionated lymphocytes. Total cellular RNA was prepared using the TriPure reagent (Roche Applied Science, Germany) followed by chloroform (Merck, Darmstadt, Germany) extraction and isopropanol (Merck, Darmstadt, Germany) precipitation. The concentration and purity of the RNA were determined by spectrophotometry and denaturing gel electrophoresis. A total of 10 μl RNA was subjected to cDNA synthesis using a kit (RevertAid First Strand cDNA Synthesis Kit, Fermentas, Waltham, MA, USA) according to the manufacturer's protocol and used for reverse transcription-polymerase chain reaction (RT-PCR). The RT-PCR reaction mix was as follows: 1.5 μl cDNA, 0.3 μl forward primer (10 pM), 0.3 μl reverse primer (10 pM), 0.3 μl of ROX , and 7.5 μl of SYBR Premix® Ex Taq qPCR Master Mix (Takara, Burlington, Japan), and 5.1 μl water. Reactions were performed in a StepOne™ Real-Time PCR System (Applied Biosystems, Foster City, CA, USA).

The cycling profile of the reaction mix was as follows: initial denaturation at 95°C for 10 s (for 40 cycles) and finally 60°C for 30 s. After each run, the result was analyzed automatically once, with StepOne software v. 2.1 (Applied Biosystems, Foster City, CA, USA). The relative standard curve method was applied for cDNA quantification. This approach gives rise to highly accurate quantitative results (quantity of an unknown sample is acquired from interpolation of the standard curves. The curve produced from the same samples for each plate). The quantity of the target genes was normalized by the quantity of glyceraldehyde 3-phosphate dehydrogenase (GAPDH) as the endogenous control gene (GAPDH was used as the housekeeping gene). To obtain the final relative quantity, the normalized quantity of the treated samples was compared with the normalized quantity of the control sample. The sequences of primers used in the RT-PCR reactions are shown in [Table 1].
Table 1: Sequence of primers used for real-time polymerase chain reaction

Click here to view

Statistical analysis

The data were analyzed using the SPSS program version 16. (SPSS Inc., Chicago, IL, USA). Independent sample Student's t-test was employed to assess if the results obtained for different groups were statistically significant (P < 0.05).

Ethical considerations

The ethical issues about the maintenance and care of experimental animals comply with the National Institutes of Health guidelines for the humane use of laboratory animals.

 > Results Top

This study examined the effect of LD (0.1 Gy), HD (2 Gy), and AR (0.1 + 2 Gy) on some immune system parameters, as shown in [Figure 1].
Figure 1: Experimental design: BALB/c mouse lymphocyte was examined for radioadaptive response after exposures. Radioadaptive response experiments, low-dose radiation was delivered as a low dose to mice before a subsequent high-dose exposure, and mice were euthanized 24 h after the high dose

Click here to view

Four groups of mice received 0, 0.1, 2, and 0.1 + 2 Gy of gamma-radiation from a cobalt-60 radiation source, respectively. Then, the spleens of mice were removed; increased dose reduced the number of lymphocytes in mouse spleen [Figure 2]. In all irradiated groups, the reduction in lymphocyte number was significant compared to the control group (P < 0.001). However, a significant increase was observed in cell number in the AR group (0.1 + 2 Gy) relative to the HD group.
Figure 2: Alterations in the cell number of lymphocyte populations following γ-irradiation. Error bars represent standard deviations. Significance of differences from 0 Gy for the corresponding dose is indicated by **(P < 0.001) and significance of difference between the adaptive and high-dose groups is indicated by ###(P < 0.0001)

Click here to view

Effects of low-dose and high-dose gamma-radiation and adaptive response on expression of interleukin-4, interferon-γ, and transforming growth factor

-β genes

First, lymphocytes were counted, RNAs of mouse lymphocytes were isolated, cDNA was synthesized, and then, relative values of IL-4, IFN-γ, and transforming growth factor (TGF)-β were obtained by quantitative RT-PCR.

There were no significant differences in expression of IL-4, IFN-γ, and TGF-β between the LD and control groups [Figure 3]. However, in the HD radiation group, IL-4 and IFN-γ gene expression was significantly reduced (P < 0.0001) and also TGF-β was significantly decreased (P < 0.001) [Figure 3]a, [Figure 3]b, [Figure 3]c. Interestingly, AR effect induced significantly different expression between the HD and AR groups for all genes (P < 0.0001). The results, as shown in [Figure 3]d, indicate that IFN-γ/IL-4 ratio in the LD group showed no significant increase relative to the control group. In the HD group, IFN-γ/IL-4 ratio showed a significant increase compared to the control group (P < 0.001). In the AR group, increased expression ratio was not significant relative to the control group and significantly decreased compared to the HD group (P < 0.0001) [Figure 3]d.
Figure 3: Changes in the cytokine expression profile of interleukin-4 (a), interferon-γ (b), transforming growth factor-β (c), and interferon-γ/interleukin-4 (d) in mice after irradiation by different doses. RNA was isolated and alterations in the cytokine expression patterns were studied by quantitative reverse transcription-polymerase chain reaction. The error bars represent standard deviations. Significance of differences from 0 Gy for the corresponding cytokine is indicated by ***(P < 0.0001) and significance of differences between the adaptive and high-dose groups is indicated by ###(P < 0.0001)

Click here to view

 > Discussion Top

Over the past two decades in addition to previously well-known effects of LD (cancer and genetic effects), it has been revealed that LDs may initiate molecular changes in irradiated and nonirradiated cells. The endpoints of these changes are known as increasing radiation resistance, AR, bystander effect, hypersensitivity, and death-inducing factor activation.[8],[9],[20],[21],[22] The principle of AR is the biological process that pretreatment by LD radiation can make an organism adapt to subsequent HD radiation and reduce the damage caused by HD irradiation in normal tissue.[21] The underlying molecular mechanisms of protective biological effects of LD radiation mainly involve enhanced DNA repair, stimulated immune regulation, and changing expression of some genes.[23],[24],[25],[26] AR indicates reduced harmful effects of HD exposure followed by a LD, confirming the usefulness of LDs. In the present study, we have examined the consequence of AR on immune system activity in mice by figuring out the expression levels of IFN-γ, IL-4, and TGF-β cytokines.

First, the number of lymphocytes in the spleen of irradiated mice was counted; it revealed reduction in number of cells in all three irradiated groups following exposure, as shown in [Figure 2]. However, According to our observations in the AR group, delivery of a HD followed by a LD of IR caused a significant increase in number of cells relative to the HD group. The decreased number of dead cells observed per spleen of the AR group mice compared to those of the HD group is an indication of potential radioadaptive effect, although it is not clear whether the decrease in the number of cells in the BALB/c strain in our study was due to a decrease in lymphocyte apoptosis or necrosis. It may be noted that exposure to LDs can cause adaptation that these results are in agreement with previous studies.[22],[27],[28],[29] In addition, in this study, a reduction in BALB/c mouse spleen cellularity was also observed following 2 Gy irradiation, which was also consistent with previous reports.[30],[31]

Radiation-induced changes in gene expression are usually considered to be early events. Gene expression profiling of immune system cytokines indicates that exposure to low doses of ionizing radiation causes a significant reduction in TGF-β, which is in agreement with the results of Bogdándi et al.[5] TGF-β acts as a potent immunosuppressive cytokine, and it influences on both cell differentiation and cell proliferation. In this study, following HD radiation after 24 h of exposure, the expression of TGF-β was significantly decreased and LD before HD reduced this effect and thus increased the immunosuppressive effects. On the other hand, exposure to HD increased apoptosis [32] and caused a substantial decrease in IL-4 and IFN-γ which, in turn, can confirm the immune system suppression as a result of receiving HDs. Our results about gene expression alteration caused by a HD are in agreement with the study of Han et al.[33] Similar gene expression for TGF-β and IL-4 was reported by Bogdándi et al.[5] In the AR group after 24 h, the expression of IL-4 was significantly decreased compared to the control group. Eventually, it can be concluded that a LD before HD decreased the enhancement of immunosuppressive effects which can be occurred due to high dosage. Treg cells have indispensable roles in immunological tolerance and protect the host from autoimmune disease and allergies as well as insignificant increase in the expression of IL-4 and IFN-γ [Figure 3]a and [Figure 3]b. The balance between inflammatory and anti-inflammatory signals is reflected by the expression patterns of IFN-γ and IL-4. Immune system responses play an important role in balance function of the human body and are divided into two groups: Th1 and Th2. Th cells represent a functionally heterogeneous population, comprising distinct subsets termed Th1 and Th2 defined by their cytokine secretion profiles. In general, cytokines produced by Th1 cells (e.g., IFN-γ and IL-2) promote both production of complement-fixing and opsonizing antibodies and macrophage activation. Cytokines produced by Th2 cells (e.g., IL-4, IL-5, IL-6, IL-10, and IL-13) stimulate antibody production and promote mast cell and eosinophil granulocyte differentiation and activation. Th1 immune responses improve the cellular immune response, but Th2 immune responses lead to enhancement of humoral immunity, production of antibodies as well as allergic reactions. Disrupted balance between Th1/Th2 (i.e., IFN-γ/IL-4 ratio) with immune-regulatory cytokines predisposes the body to diseases such as autoimmunity, chronic infections, severe depression, and atherosclerosis and can cause allergy as well as increasing its severity. Changing balance of the immune system plays an important role in pathophysiology of some diseases, including asthma, autoimmunity, and cancer.[4] In this study, the expression ratio of IFN-γ/IL-4 genes was significantly increased after a HD. According to previous descriptions, the immune response shifts toward higher production of Th1 lymphocytes and enhances the cellular immune response, which may deduction that the patient will be susceptible to autoimmune diseases after receiving the HDs.[34] Fang et al. observed reduced IFN-γ/IL-4 ratio by studying the effect of a 0.5 Gy of gamma-radiation on cytokine levels in mice.[35] Chronic exposure to LDs with a total dose of 0.2 Gy also reduced the ratio of IFN-γ/IL-4 compared to corresponding values in the control group.[36] On the other hand, our result showed that LD did not cause a significant change in this ratio. In the AR group, the IFN-γ/IL-4 ratio was significantly reduced compared to the HD group. This is indicating that the LDs delivered before the HD have neutralized the harmful effects of challenge dose. The immune response has not shifted toward Th1 and/or Th2 responses. Consistent with these results, in our previous study, it was shown that LD can cause radioresistancy in lymphocytes.[29] As some of the previous studies that were conducted to investigate the adaptive effect and showed that this phenomenon can occur,[2],[16],[37] our study can confirm the induction of such response in the immune system.

 > Conclusion Top

In this study, we have investigated the in vivo AR of the immune system. For this purpose, some of the important cytokines in the immune response that are representing immune system functions were measured. The results of the present study have shown that LD causes resistance in lymphocytes. Induction of AR by LD was previously seen in Th1 and Th2 cells and causes changes in the expression of genes affecting these two main cell types of the immune system. Adaptive dose leads to reduced level of inflammatory cytokines and prevents the shift of immune response, minimizing the possibility of autoimmune and inflammatory diseases as well as allergic reactions after receiving the HD. The results of this work further confirm that AR does happen.


We would like to give our sincere appreciation to the reviewers for their helpful comments on this article. This article is based on the results extracted from a M. Sc. thesis (code no: 911185) presented to the Medical Physics Department of Mashhad University of Medical Sciences (MUMS).

Financial support and sponsorship

The authors would like to thank the office of the Vice-President for Research Affairs of MUMS for funding this work.

Conflicts of interest

There are no conflicts of interest.

 > References Top

Olivieri G, Bodycote J, Wolff S. Adaptive response of human lymphocytes to low concentrations of radioactive thymidine. Science 1984;223:594-7.  Back to cited text no. 1
Manesh SS, Sangsuwan T, Wojcik A, Haghdoost S. Studies of adaptive response and mutation induction in MCF-10A cells following exposure to chronic or acute ionizing radiation. Mutat Res 2015;780:55-9.  Back to cited text no. 2
Shirazi MM, Shabestani-Monfared A, Shahidi M, Amiri M, Abedi SM, Borzoueisileh S, et al. Radio-adaptive response in myocardial perfusion imaging induced by technetium-99m. Indian J Nucl Med 2017;32:7-10.  Back to cited text no. 3
[PUBMED]  [Full text]  
Noack M, Miossec P. Th17 and regulatory T cell balance in autoimmune and inflammatory diseases. Autoimmun Rev 2014;13:668-77.  Back to cited text no. 4
Bogdándi EN, Balogh A, Felgyinszki N, Szatmári T, Persa E, Hildebrandt G, et al. Effects of low-dose radiation on the immune system of mice after total-body irradiation. Radiat Res 2010;174:480-9.  Back to cited text no. 5
Bahreyni-Toossi MT, Vosoughi H, Azimian H, Rezaei AR, Momennezhad M.In vivo exposure effects of 99mTc-methoxyisobutylisonitrile on the FDXR and XPA Genes expression in human peripheral blood lymphocytes. Asia Ocean J Nucl Med Biol 2018;6:32-40.  Back to cited text no. 6
Mitchel RE. The dose window for radiation-induced protective adaptive responses. Dose Response 2009;8:192-208.  Back to cited text no. 7
Kalantari H, Motamed N, Mohseni Meybodi A, Jabbari Arfaie A, Baharvand H, Gourabi H. The response of mouse embryonic stem cells to low doses of γ-radiation: Evidence for an adaptive response. Mutat Res Genet Toxicol Environ Mutagen 2014;761:44-7.  Back to cited text no. 8
Komova O, Krasavin E, Nasonova E, Mel'nikova L, Shmakova N, Cunha M, et al. Relationship between radioadaptive response and individual radiosensitivity to low doses of gamma radiation: An extended study of chromosome damage in blood lymphocytes of three donors. Int J Radiat Biol 2018;94:54-61.  Back to cited text no. 9
Borzoueisileh S, Monfared SA. Natural background radiations radioadaptive response and radiation hormesis. BabolJ bums 2015;17:15-21.  Back to cited text no. 10
Braun CM, Huang SK, Bashian GG, Kagey-Sobotka A, Lichtenstein LM, Essayan DM. Corticosteroid modulation of human, antigen-specific Th1 and Th2 responses. J Allergy Clin Immunol 1997;100:400-7.  Back to cited text no. 11
Cosmi L, Liotta F, Maggi E, Romagnani S, Annunziato F. Th17 cells: New players in asthma pathogenesis. Allergy 2011;66:989-98.  Back to cited text no. 12
Askari VR, Rezaee SA, Abnous K, Iranshahi M, Boskabady MH. The influence of hydro-ethanolic extract of Portulaca oleracea L. on Th1/Th2 balance in isolated human lymphocytes. J Ethnopharmacol 2016;194:1112-21.  Back to cited text no. 13
Kianmehr M, Rezaei A, Hosseini M, Khazdair MR, Rezaee R, Askari VR, et al. Immunomodulatory effect of characterized extract of Zataria multiflora on Th1, Th2and Th17 in normal and Th2 polarization state. Food Chem Toxicol 2017;99:119-27.  Back to cited text no. 14
Bazyka D, Chumak A, Byelyaeva N, Gulaya N, Margytich V, Thevenon C, et al. Immune cells in Chernobyl radiation workers exposed to low-dose irradiation. Int J Low Radiat 2003;1:63-75.  Back to cited text no. 15
Toprani SM, Das B. Radio-adaptive response of base excision repair genes and proteins in human peripheral blood mononuclear cells exposed to gamma radiation. Mutagenesis 2015;30:663-76.  Back to cited text no. 16
Otsuka K, Koana T, Tauchi H, Sakai K. Activation of antioxidative enzymes induced by low-dose-rate whole-body gamma irradiation: Adaptive response in terms of initial DNA damage. Radiat Res 2006;166:474-8.  Back to cited text no. 17
Liu SZ. Cancer control related to stimulation of immunity by low-dose radiation. Dose Response 2006;5:39-47.  Back to cited text no. 18
Manda K, Glasow A, Paape D, Hildebrandt G. Effects of ionizing radiation on the immune system with special emphasis on the interaction of dendritic and T cells. Front Oncol 2012;2:102.  Back to cited text no. 19
Bonner WM. Phenomena leading to cell survival values which deviate from linear-quadratic models. Mutat Res 2004;568:33-9.  Back to cited text no. 20
Tang FR, Loke WK. Molecular mechanisms of low dose ionizing radiation-induced hormesis, adaptive responses, radioresistance, bystander effects, and genomic instability. Int J Radiat Biol 2015;91:13-27.  Back to cited text no. 21
Bahreyni-Toossi MT, Azimian H, Rezaei AR, Rafatpanah H, Hamzehloei T, Fardid R. Low-dose irradiation alters the radio-sensitivity of human peripheral blood lymphocytes. In: World Congress on Medical Physics and Biomedical Engineering. Beijing, China: Springer; 2013.  Back to cited text no. 22
Feinendegen LE, Pollycove M, Sondhaus CA. Responses to low doses of ionizing radiation in biological systems. Nonlinearity Biol Toxicol Med 2004;2:143-71.  Back to cited text no. 23
Bodnarchuk IA. Analysis of the role of DNA repair, regulation of cell cycle and apoptosis in the radiation-induced adaptive response of mammalian cells. Radiats Biol Radioecol 2003;43:19-28.  Back to cited text no. 24
Chen SL, Cai L, Meng QY, Xu S, Wan H, Liu SZ. Low-dose whole-body irradiation (LD-WBI) changes protein expression of mouse thymocytes: Effect of a LD-WBI-enhanced protein RIP10 on cell proliferation and spontaneous or radiation-induced thymocyte apoptosis. Toxicol Sci 2000;55:97-106.  Back to cited text no. 25
Ishii K, Misonoh J. Induction of radio-adaptive response by low-dose X-irradiation on chromosome aberrations in human embryonic fibroblasts. Physiol Chem Phys Med NMR 1996;28:83-90.  Back to cited text no. 26
Qu Y, Jin S, Zhang A, Zhang B, Shi X, Wang J, et al. Gamma-ray resistance of regulatory CD4+CD25+Foxp3+ T cells in mice. Radiat Res 2010;173:148-57.  Back to cited text no. 27
Payne CM, Bjore CG Jr., Schultz DA. Change in the frequency of apoptosis after low- and high-dose X-irradiation of human lymphocytes. J Leukoc Biol 1992;52:433-40.  Back to cited text no. 28
Azimian H, Bahreyni-Toossi MT, Rezaei AR, Rafatpanah H, Hamzehloei T, Fardid R. Up-regulation of Bcl-2 expression in cultured human lymphocytes after exposure to low doses of gamma radiation. J Med Phys 2015;40:38-44.  Back to cited text no. 29
[PUBMED]  [Full text]  
Bannister LA, Mantha RR, Devantier Y, Petoukhov ES, Brideau CL, Serran ML, et al. Dose and radioadaptive response analysis of micronucleus induction in mouse bone marrow. Int J Mol Sci 2016;17. pii: E1548.  Back to cited text no. 30
Pecaut MJ, Nelson GA, Gridley DS. Dose and dose rate effects of whole-body gamma-irradiation: I. Lymphocytes and lymphoid organs. In vivo 2001;15:195-208.  Back to cited text no. 31
Azimian H, Dayyani M, Toossi MTB, Mahmoudi M. Bax/Bcl-2 expression ratio in prediction of response to breast cancer radiotherapy. Iran J Basic Med Sci 2018;21:325-32.  Back to cited text no. 32
Han SK, Song JY, Yun YS, Yi SY. Effect of gamma radiation on cytokine expression and cytokine-receptor mediated STAT activation. Int J Radiat Biol 2006;82:686-97.  Back to cited text no. 33
Bahreyni-Toossi MT, Najafi-Amiri M, Sankian M, Azimian H, Abdollahi-Dehkordi S, Khademi S. INF/IL-4 increases after the low doses of gamma radiation in BALB/c spleen lymphocytes. Iranian Journal of Medical Physics 2019;16:264-9.  Back to cited text no. 34
Fang SP, Tago F, Tanaka T, Simura N, Muto Y, Goto R, et al. Repeated irradiations with gamma-rays at a Dose of 0.5 Gy may exacerbate asthma. J Radiat Res 2005;46:151-6.  Back to cited text no. 35
Shin SC, Lee KM, Kang YM, Kim K, Kim CS, Yang KH, et al. Alteration of cytokine profiles in mice exposed to chronic low-dose ionizing radiation. Biochem Biophys Res Commun 2010;397:644-9.  Back to cited text no. 36
Hou J, Wang F, Kong P, Yu PK, Wang H, Han W. Gene profiling characteristics of radioadaptive response in AG01522 normal human fibroblasts. PLoS One 2015;10:e0123316.  Back to cited text no. 37


  [Figure 1], [Figure 2], [Figure 3]

  [Table 1]


Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

  >Abstract>Introduction>Materials and Me...>Results>Discussion>Conclusion>Article Figures>Article Tables
  In this article

 Article Access Statistics
    PDF Downloaded56    
    Comments [Add]    

Recommend this journal