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Changes in immune parameters and lymphocyte ATP level of peripheral blood in residents of the North during short-term cold exposure to the body

https://doi.org/10.25789/YMJ.2020.72.22

Abstract

The immune system constantly responds to various environmental stimuli. The aim of the study was to investigate immune effects of short-term cold exposure taking into account ATP level in peripheral blood lymphocytes in healthy residents of the North. So, the total number of lymphocytes and their phenotypes, as well as the content of cytokines and the concentration of ATP in the lymphocytes were determined in 38 volunteers twice (before and after their short-term stay for 5 minutes in a cold chamber at t = -25°C). Cluster analysis revealed two statistically different groups. The first group with an initially higher ATP level in lymphocytes responded to hypothermia by lower ATP concentration with the unchanging total number of lymphocytes as well as by a decrease in predominantly CD16+ killer-cells. The other group reacted by an increase in ATP concentration with a decrease in the number of lymphocytes and by a pronounced decrease in CD4+ helper-cells and in CD71+ cells with a transferrin receptor. Also, the proinflammatory cytokines TNFα and IL-6 increased in the first group, while the second group showed a decrease in the level of lymphocyte-activating cytokine IL-1β. It can be assumed that the response to hypothermia in the first group is provided through the CIRP-NFkB-TNFα axis and leads to an increase in the risk of non-infectious inflammation. For the second group, a protective mechanism is triggered to restrain lymphocyte activity and the development of T-cell-mediated inflammation through regulation by means of T-effector and T-regulatory cells AMPK balance, autophagy, mitophagy and mitochondrial biogenesis. The study of the immune response to hypothermia is important for understanding the cellular mechanisms of adaptation as well as for the search of targets to correct the immune response.

About the Authors

O. V. Zubatkina
Institute of Environmental Physiology of N. Laverov Federal Center for Integrated Arctic Research Ural Department of Russian Academy of Sciences
Russian Federation

Zubatkina Olga Vladimirovna - PhD, professor, research scientist of the laboratory Ecological immunology

163061, Arkhangelsk, Lomonosov ave., 249. Phone number: +79214953695



L. K. Dobrodeeva
Institute of Environmental Physiology of N. Laverov Federal Center for Integrated Arctic Research Ural Department of Russian Academy of Sciences
Russian Federation

Dobrodeeva Liliya Konstantinovna - professor, chief scientist of the laboratory Ecological immunology

163061, Arkhangelsk, Lomonosov ave., 249. Phone number: 65-29-95



S. D. Kruglov
Institute of Environmental Physiology of N. Laverov Federal Center for Integrated Arctic Research Ural Department of Russian Academy of Sciences
Russian Federation

Kruglov Sergey Dmitrievich - full-time postgraduate student of the laboratory Ecological immunology

163061, Arkhangelsk, Lomonosov ave., 249. Phone number: +79210782348



References

1. Al-Fageeh M.B. Alternative promoters regulate cold inducible RNA-binding (CIRP) gene expression and enhance transgene expression in mammalian cells / M.B. Al-Fageeh, C.M. Smales // Mol. Biotechnol. – 2013. – Vol. 54(2). – P. 238–249. DOI: 10.1007/s12033-013-9649-5.

2. AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1 / J. Kim, M. Kundu, B. Viollet, K.L. Guan // Nat. Cell Biol. – 2011. – Vol. 13(2). – P. 132–141. DOI: 10.1038/ncb2152.

3. Bertin S. Transient Receptor Potential (TRP) channels in T cells / S. Bertin, E. Raz // Semin. Immunopathol. – 2016. – Vol. 38(3). – P. 309–319. DOI: 10.1007/s00281-015-0535-z.

4. Canto C. PGC-1alpha, SIRT1 and AMPK, an energy sensing network that controls energy expenditure / C. Canto, J. Auwerx // Curr. Opin. Lipidol. – 2009. – Vol. 20(2). – P. 98–105. DOI: 10.1097/MOL.0b013e328328d0a4.

5. Combined inhibition of NF-kB and Bcl-2 triggers synergistic reduction of viability and induces apoptosis in melanoma cells / M. Watanabe, K. Umezawa, M. Higashihara [et al.] // Oncol. Res. Featur. Preclin. Clin Cancer Therap. – 2014. – Vol. 21(2). – P. 173–180. DOI: 10.3727/096504014X13887748696707.

6. De novo fatty acid synthesis controls the fate between regulatory T and T helper 17 cells / L. Berod, C. Friedrich, A. Nandan [et al.] // Nat. Med. – 2014. – Vol. 20(11). – P. 1327–1333. DOI: 10.1038/nm.3704

7. Garcia D. AMPK: Mechanisms of Cellular Energy Sensing and Restoration of Metabolic Balance / D. Garcia, J.S. Reuben // Molecular Cell. – 2017. – Vol. 66(6). – P. 789–799. DOI: 10.1016/j.molcel.2017.05.032.

8. Involvement of TRPV3 and TRPM8 ion channel proteins in induction of mammalian cold-inducible proteins / T. Fujita, Y. Liu, H. Higashitsuji [et al.] // Biochemical and Biophysical Research Communications. – 2016. – Vol. 495(1). – P. 935–940. DOI: 10.1016/j.bbrc.2017.11.136.

9. Kantari C. Caspase-8 and bid: caught in the act between death receptors and mitochondria / C. Kantari, H. Walczak // Biochim. Biophys. Acta. (BBA)-Mol. Cell. Res. – 2011. – Vol. 1813(4). – P. 558–563. DOI: 10.1016/j.bbamcr.2011.01.026.

10. Kelvin J. Adaptive homeostasis / J. Kelvin, A. Davies // Mol. Aspects Med. – Vol. 49(6). – P. 1–7. DOI: 10.1016/j.mam.2016.04.007.

11. Metabolism. AMP-activated protein kinase mediates mitochondrial fission in response to energy stress / E.Q. Toyama, S. Herzig, J. Courchet [et al.] // Science. – 2016. – Vol. 351(6270). – P. 275 – 281. DOI: 10.1126/science.aab4138.

12. NF-kappaB-dependent role for cold-inducible RNA binding protein in regulating interleukin 1beta. / C. Brochu, M.A. Cabrita, B.D. Melanson [et al.] // PloS One. – 2013. – Vol. 141(11). – P. e57426. DOI: 10.1371/journal.pone.0057426.

13. O’Neill L.A. Metabolism of inflammation limited by AMPK and pseudo-starvation / L.A. O’Neill, D.G. Hardie // Nature. – 2013. – Vol. 493(7432). – P. 346–355. DOI: 10.1038/nature11862.

14. The energy sensor AMPK regulates T cell metabolic adaptation and effector responses in vivo / J. Blagih, F. Coulombe, E.E. Vincent [et al.] // Immunity. – 2015. – Vol. 42(1). – P. 41–54. DOI: 10.1016/j.immuni.2014.12.030.

15. The role of AMPK in T cell metabolism and function / E.H. Ma, M.C. Poffenberger, A.H. Wong, R.G. Jones // Current Opinion in Immunology – 2017. – Vol. 46. – P. 45–52. DOI: 10.1016/j.coi.2017.04.004.

16. The role of cold‐inducible RNA binding protein in cell stress response / Y. Liao, L. Tong, L. Tang, S. Wu // Int. J. Cancer. – 2017. – Vol. 141(11). – P. 2164–2173. DOI: 10.1002/ijc.30833.

17. Zhu X. Cold-inducible proteins CIRP and RBM3, a unique couple with activities far beyond the cold / X. Zhu, C. Buhrer, S. Wellmann. // Cellular and Molecular Life Sciences. – 2016. – Vol. 73(20). – P. 3839–3859. DOI: 10.1007/s00018-016-2253-7.


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For citations:


Zubatkina O.V., Dobrodeeva L.K., Kruglov S.D. Changes in immune parameters and lymphocyte ATP level of peripheral blood in residents of the North during short-term cold exposure to the body. Yakut Medical Journal. 2020;(4):90-93. https://doi.org/10.25789/YMJ.2020.72.22

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