Abstract

BackgroundNatural killer cells (NK cells) are cytotoxic lymphocytes of innate immunity that reveal some immunoregulatory properties, however, their role in the process of ageing is not completely understood. The study aimed to analyze the expression of proteins involved in cellular stress response: sirtuin 1 (SIRT1), heat shock protein 70 (HSP70) and manganese superoxide dismutase (SOD2) in human NK cells with reference to the process of ageing. Non-stimulated and stimulated with IL-2, LPS or PMA with ionomycin cells originated from peripheral blood samples of: seniors aged over 85 (‘the oldest’; n = 25; 88.5 ± 0.5 years, mean ± SEM), seniors aged under 85 (‘the old’; n = 30; 75.6 ± 0.9 years) and the young (n = 31; 20.9 ± 0.3 years). The relationships between the levels of expression of cellular protective proteins in the studied population were also analyzed. The concentrations of carbonyl groups and 8-isoprostanes, markers of oxidative stress, in both stimulated and non-stimulated cultured NK cells were measured to assess the level of the oxidative stress in the cells.ResultsThe oldest seniors varied from the other age groups by significantly higher expression of SIRT1 and HSP70 both in non-stimulated and stimulated NK cells. These cells also appeared to be resistant to further stimulations with IL-2, LPS or PMA with ionomycin. Highly positive correlations between SIRT1 and intracellular HSP70 in both stimulated and non-stimulated NK cells were observed. SOD2 presented low expression in non-stimulated cells, whereas its sensitivity to stimulation increased with age of donors. High positive correlations between SOD2 and surface HSP70 were observed. We found that the markers of oxidative stress in NK cells did not change with ageing.ConclusionsThe oldest seniors revealed well developed adaptive stress response in NK cells with increased, constant levels of SIRT1 and intracellular HSP70. They presented also very high positive correlations between expression of these cellular protective proteins both in stimulated and non-stimulated cells. These phenomena may contribute to the long lifespan of this group of elderly. Interestingly, in NK cells SOD2 revealed a distinct role in cellular stress response since it showed sensitivity to stimulation increasing with age of participants. These observations provide novel data concerning the role of NK cells in the process of ageing.

Highlights

  • Natural killer cells (NK cells) are cytotoxic lymphocytes of innate immunity that reveal some immunoregulatory properties, their role in the process of ageing is not completely understood

  • Toll-like receptors 4 (TLR4) interacts by binding lipid A, a part of LPS molecule what results in activation of Nuclear factor kappalight-chain-enhancer of activated B cells (NF-κB) pathway and expression of genes coding for proinflammatory cytokines, e.g. TNF, IL-1, IL-6, Granulocyte macrophage colony - stimulating factor (GM-CSF) and chemokines, e.g. IL-8, Regulated on activation (RANTES), Macrophage inflammatory protein (MIP)-1α, Macrophage chemoattractant protein (MCP)-1 [15, 16]

  • We analyzed NK cells isolated from peripheral blood samples of different age groups

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Summary

Introduction

Natural killer cells (NK cells) are cytotoxic lymphocytes of innate immunity that reveal some immunoregulatory properties, their role in the process of ageing is not completely understood. Natural killer cells (NK cells) are cytotoxic lymphocytes of innate immune system They are cytotoxic ILCs1 (innate lymphoid cells type 1) crucial for immune response against viral infection and tumor cells [1, 2] but demonstrate some immunoregulatory activities by secretion of cytokines and chemokines [3, 4]. They may adjust to the alterations of the cellular environment and develop a type of antigen-specific immunological memory exposing characteristics of both innate and adaptive immunity [5, 6]. TLR4 interacts by binding lipid A, a part of LPS molecule what results in activation of NF-κB pathway and expression of genes coding for proinflammatory cytokines, e.g. TNF, IL-1, IL-6, GM-CSF and chemokines, e.g. IL-8, RANTES, MIP-1α, MCP-1 [15, 16]

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