Vol 55, No 1 (2017)
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Published online: 2017-04-28

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Influence of oxygen concentration on T cell proliferation and susceptibility to apoptosis in healthy men and women

Agnieszka Waskowska, Katarzyna A. Lisowska1, Agnieszka Daca, Izabella Henc, Fredrik Brandberg, Paula Mazurek, Edyta Brzustewicz, Jacek M. Witkowski, Ewa Bryl
Pubmed: 28509314
Folia Histochem Cytobiol 2017;55(1):26-36.

Abstract

Introduction. Much of what we know about the functioning of human T lymphocytes is based on the experiments carried out in atmospheric oxygen (O2) concentrations, which are significantly higher than those maintained in blood. Interestingly, the gender differences in the activity of T cells and their susceptibility to apoptosis under different O2 conditions have not yet been described. The aim of the study was to compare two main markers of lymphocyte function: proliferation capacity and ability to produce cytokines as well as their susceptibility to apoptosis under two different O2 concentrations, between men and women.

Materials and methods. 25 healthy volunteers, both males (13) and females (12) were recruited to the study (mean age 25.48 ± 5.51). By using cytometry proliferation parameters of human CD4+ CD28+ cells or CD8+CD28+ cells in response to polyclonal stimulation of the TCR/CD3 complex at atmospheric (21%) and physiological (10%) O2 concentrations using our modified dividing cell tracking technique (DCT) were analyzed as well as the percentages of apoptotic cells. We also determined the levels of IFN-γ, IL-2, IL-10 and IL-17A using Cytometric Bead Array Flex system in cell culture supernatants.

Results. CD4+CD28+ and CD8+CD28+ cells from the whole study group were characterized by shorter time required to enter the first (G1) phase of the first cell cycle at 21% compared to 10% O2. Both T cell populations performed significantly more divisions at 21% O2. The percentages of dividing cells were also significantly higher at atmospheric O2. Interestingly, data analysis by gender showed that male lymphocytes had similar proliferative parameters at both O2 concentrations while female lymphocytes proliferate more efficiently (note from the author: we cannot say that lymphocytes proliferate faster, rather more effectively, because cells perform more divisions, which gives more percentage of offspring cells) at 21% oxygen. Compared to males, the female CD4+ cells showed increased susceptibility to apoptosis at both O2 concentrations. No differences in the levels of cytokines regardless of gender and oxygen conditions were found.

Conclusions. We showed that in vitro female T cells (both CD4+ and CD8+ cells) are more sensitive than male lymphocytes to low O2 concentration as demonstrated by the decrease in their proliferation dynamics. The effect does not depend on increased apoptosis of female T cells under low O2 because percentage of apoptotic cells was similar at both O2 concentrations.

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References

  1. Kurz H, Sandau K, Christ B. On the bifurcation of blood vessels-Wilhelm Roux's doctoral thesis (Jena 1878)--a seminal work for biophysical modelling in developmental biology. Ann Anat. 1997; 179(1): 33–36.
  2. Ronen D, Benvenisty N. Sex-dependent gene expression in human pluripotent stem cells. Cell Rep. 2014; 8(4): 923–932.
  3. Campesi I, Capobianco G, Dessole S, et al. Estrogenic compounds have divergent effects on human endothelial progenitor cell migration according to sex of the donor. J Vasc Res. 2015; 52(4): 273–278.
  4. Ahmedi ML, Belguendouz H, Messaoudene D, et al. [Influence of steroid hormones on the production of two inflammatory markers, IL-12 and nitric oxide, in Behçet's disease]. J Fr Ophtalmol. 2016; 39(4): 333–340.
  5. Durazzo M, Belci P, Collo A, et al. Gender specific medicine in liver diseases: a point of view. World J Gastroenterol. 2014; 20(9): 2127–2135.
  6. Panchanathan R, Shen H, Zhang X, et al. Mutually positive regulatory feedback loop between interferons and estrogen receptor-α in mice: implications for sex bias in autoimmunity. PLoS ONE. 2010; 5(5): e10868.
  7. Hill L, Jeganathan V, Chinnasamy P, et al. Differential roles of estrogen receptors α and β in control of B-cell maturation and selection. Mol Med. 2011; 17(3-4): 211–220.
  8. Maret A, Coudert JD, Garidou L, et al. Estradiol enhances primary antigen-specific CD4 T cell responses and Th1 development in vivo. Essential role of estrogen receptor alpha expression in hematopoietic cells. Eur J Immunol. 2003; 33(2): 512–521.
  9. Correale J, Arias M, Gilmore W. Steroid hormone regulation of cytokine secretion by proteolipid protein-specific CD4+ T cell clones isolated from multiple sclerosis patients and normal control subjects. J Immunol. 1998; 161(7): 3365–3374.
  10. Lissauer D, Eldershaw SA, Inman CF, et al. Progesterone promotes maternal-fetal tolerance by reducing human maternal T-cell polyfunctionality and inducing a specific cytokine profile. Eur J Immunol. 2015; 45(10): 2858–2872.
  11. Lee JH, Lydon JP, Kim CH. Progesterone suppresses the mTOR pathway and promotes generation of induced regulatory T cells with increased stability. Eur J Immunol. 2012; 42(10): 2683–2696.
  12. Zielniok K, Gajewska M, Motyl T. Molecular actions of 17β-estradiol and progesterone and their relationship with cellular signaling pathways. Postępy Higieny i Medycyny Doświadczalnej. 2014; 68: 777–792.
  13. Athreya BH, Pletcher J, Zulian F, et al. Subset-specific effects of sex hormones and pituitary gonadotropins on human lymphocyte proliferation in vitro. Clin Immunol Immunopathol. 1993; 66(3): 201–211.
  14. Stopińska-Głuszak U, Waligóra J, Grzela T, et al. Effect of estrogen/progesterone hormone replacement therapy on natural killer cell cytotoxicity and immunoregulatory cytokine release by peripheral blood mononuclear cells of postmenopausal women. J Reprod Immunol. 2006; 69(1): 65–75.
  15. Villacres MC, Longmate J, Auge C, et al. Predominant type 1 CMV-specific memory T-helper response in humans: evidence for gender differences in cytokine secretion. Hum Immunol. 2004; 65(5): 476–485.
  16. Steurer J, Hoffmann U, Dür P, et al. Changes in arterial and transcutaneous oxygen and carbon dioxide tensions during and after voluntary hyperventilation. Respiration. 1997; 64(3): 200–205.
  17. McKeown SR. Defining normoxia, physoxia and hypoxia in tumours-implications for treatment response. Br J Radiol. 2014; 87(1035): 20130676.
  18. Atkuri KR, Herzenberg LA, Niemi AK, et al. Importance of culturing primary lymphocytes at physiological oxygen levels. Proc Natl Acad Sci U S A. 2007; 104(11): 4547–4552.
  19. McNamee EN, Korns Johnson D, Homann D, et al. Hypoxia and hypoxia-inducible factors as regulators of T cell development, differentiation, and function. Immunol Res. 2013; 55(1-3): 58–70.
  20. Kulkarni A, Kuppusamy P, Parinandi N. Oxygen, the Lead Actor in the Pathophysiologic Drama: Enactment of the Trinity of Normoxia, Hypoxia, and Hyperoxia in Disease and Therapy. Antioxidants & Redox Signaling. 2007; 9(10): 1717–1730.
  21. Atkuri KR, Herzenberg LA, Herzenberg LA. Culturing at atmospheric oxygen levels impacts lymphocyte function. Proc Natl Acad Sci U S A. 2005; 102(10): 3756–3759.
  22. Krieger JA, Landsiedel JC, Lawrence DA. Differential in vitro effects of physiological and atmospheric oxygen tension on normal human peripheral blood mononuclear cell proliferation, cytokine and immunoglobulin production. Int J Immunopharmacol. 1996; 18: 545–552.
  23. Naldini A, Carraro F, Silvestri S, et al. Hypoxia affects cytokine production and proliferative responses by human peripheral mononuclear cells. J Cell Physiol. 1997; 173(3): 335–342, doi: 10.1002/(SICI)1097-4652(199712)173:3<335::AID-JCP5>3.0.CO;2-O.
  24. Carswell KS, Weiss JW, Papoutsakis ET. Low oxygen tension enhances the stimulation and proliferation of human T lymphocytes in the presence of IL-2. Cytotherapy. 2000; 2(1): 25–37.
  25. Larbi A, Zelba H, Goldeck D, et al. Induction of HIF-1alpha and the glycolytic pathway alters apoptotic and differentiation profiles of activated human T cells. J Leukoc Biol. 2010; 87(2): 265–273.
  26. Makino Y, Nakamura H, Ikeda E, et al. Hypoxia-inducible factor regulates survival of antigen receptor-driven T cells. J Immunol. 2003; 171(12): 6534–6540.
  27. Abbas Ak, Lichtman AH. Basic Immunology: Functions and Disorders of the immune System. 3rd ed. Saunders Elsevier, Philadelphia 2011.
  28. Zolnierowicz J, Ambrozek-Latecka M, Kawiak J, et al. Monitoring cell proliferation in vitro with different cellular fluorescent dyes. Folia Histochem Cytobiol. 2013; 51(3): 193–200.
  29. Witkowski JM. Advanced application of CFSE for cellular tracking. Curr Protoc Cytom. 2008; Chapter 9: Unit 9.25.
  30. Xu Y, Chaudhury A, Zhang M, et al. Glycolysis determines dichotomous regulation of T cell subsets in hypoxia. J Clin Invest. 2016; 126(7): 2678–2688.
  31. Sitkovsky M, Lukashev D. Regulation of immune cells by local-tissue oxygen tension: HIF1 alpha and adenosine receptors. Nat Rev Immunol. 2005; 5(9): 712–721.
  32. Semenza GL. HIF-1 and tumor progression: pathophysiology and therapeutics. Trends Mol Med. 2002; 8(4 Suppl): S62–S67.
  33. Nakamura H, Makino Y, Okamoto K, et al. TCR engagement increases hypoxia-inducible factor-1 alpha protein synthesis via rapamycin-sensitive pathway under hypoxic conditions in human peripheral T cells. J Immunol. 2005; 174(12): 7592–7599.
  34. Larbi A, Cabreiro F, Zelba H, et al. Reduced oxygen tension results in reduced human T cell proliferation and increased intracellular oxidative damage and susceptibility to apoptosis upon activation. Free Radic Biol Med. 2010; 48(1): 26–34.
  35. Haddad H, Windgassen D, Ramsborg CG, et al. Molecular understanding of oxygen-tension and patient-variability effects on ex vivo expanded T cells. Biotechnol Bioeng. 2004; 87(4): 437–450.
  36. Lee S, Kim J, Jang B, et al. Fluctuation of peripheral blood T, B, and NK cells during a menstrual cycle of normal healthy women. J Immunol. 2010; 185(1): 756–762.
  37. Faas M, Bouman A, Moesa H, et al. The immune response during the luteal phase of the ovarian cycle: a Th2-type response? Fertil Steril. 2000; 74(5): 1008–1013.
  38. Zampino M, Yuzhakova M, Hansen J, et al. Sex-related dimorphic response of HIF-1 alpha expression in myocardial ischemia. Am J Physiol Heart Circ Physiol. 2006; 291(2): H957–H964.
  39. Crabbe DL, Dipla K, Ambati S, et al. Gender differences in post-infarction hypertrophy in end-stage failing hearts. J Am Coll Cardiol. 2003; 41(2): 300–306.