Acute exercise preferentially redeploys NK-cells with a highly-differentiated phenotype and augments cytotoxicity against lymphoma and multiple myeloma target cells. Part II: Impact of latent cytomegalovirus infection and catecholamine sensitivity

被引:35
作者
Bigley, Austin B. [1 ]
Rezvani, Katayoun [2 ]
Pistillo, Mira [1 ]
Reed, Justin [1 ]
Agha, Nadia [1 ]
Kunz, Hawley [1 ]
O'Connor, Daniel P. [1 ]
Sekine, Takuya [2 ]
Bollard, Catherine M. [3 ,4 ]
Simpson, Richard J. [1 ]
机构
[1] Univ Houston, Dept Hlth & Human Performance, Lab Integrated Physiol, Houston, TX 77204 USA
[2] Univ Texas MD Anderson Canc Ctr, Div Canc Med, Dept Stem Cell Transplantat, Houston, TX 77030 USA
[3] Childrens Natl Hlth Syst, Program Cell Enhancement & Technol Immunotherapy, Sheikh Zayed Inst Pediat Surg Innovat, Washington, DC 20010 USA
[4] Childrens Natl Hlth Syst, Ctr Canc & Immunol Res, Washington, DC 20010 USA
关键词
Immunology; NKG2C; CD57; Isoproterenol; Cyclic AMP; Beta adrenergic receptor; NATURAL-KILLER-CELLS; MENSTRUAL-CYCLE; EXPRESSION; RECEPTORS; BINDING;
D O I
10.1016/j.bbi.2014.12.027
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We showed previously that acute exercise is associated with a preferential redeployment of highly-differentiated NK-cells and increased cytotoxicity against HLA-expressing tumor cell lines during exercise recovery. In this part II study, we retrospectively analyzed these findings in the context of latent cytomegalovirus (CMV) infection and performed additional experiments to explore potential mechanisms underpinning the marked reduction in NK-cell redeployment with exercise in CMV-seropositive individuals. We show here that latent CMV infection impairs NK-cell mobilization with exercise, only when the intensity of the exercise bout exceeds the individual blood lactate threshold (BLT). This impaired mobilization is associated with increased proportions of poorly exercise-responsive NK-cell subsets (NKG2C+/KIR-, NKG2C+/NKG2A-, and NKG2C+/CD57+) and decreased NK-cell beta(2)-adrenergic receptor (AR) expression in those with CMV. As a result, NK-cell production of cyclic AMP (cAMP) in response to in vitro isoproterenol (synthetic p-agonist) stimulation was drastically lower in those with CMV (6.0 vs. 203 pmol/mL, p < 0.001) and correlated highly with the proportion of NKG2C+/CD57+ NK-cells (R-2 = 0.97). Moreover, NK-cell cytotoxic activity (NKCA) against the K562 (36.6% vs. 22.7%, p < 0.05), U266 (23.6% vs. 15.9%, p < 0.05), and 221.AEH (41.3% vs. 13.3%, p < 0.001) cell lines was increased at baseline in those infected with CMV; however, latent CMV infection abated the post-exercise increase in NKCA as a result of decreased NK-cell mobilization. Additionally, NKCA per cell against the U266 (0.24 vs. 0.12, p < 0.01), RPMI-8226 (0.17 vs. 0.11, p < 0.05), and 221.AEH (0.18 vs. 0.11, p < 0.05) cell lines was increased 1 h post-exercise (relative to baseline) in CMV-seronegative subjects, but not in those infected with CMV. Collectively, these data indicate that latent CMV infection may compromise NK-cell mediated immunosurveillance after acute exercise due to an increased proportion of "CMV-specific" NK-cell subsets with impaired beta-adrenergic receptor signaling pathways. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:59 / 65
页数:7
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