Department of Chemistry, Tennessee State University, Nashville, TN 37209, USA.
J Immunotoxicol. 2009 Dec;6(4):285-92. doi: 10.3109/15476910903258260.
Human natural killer (NK) cells are lymphocytes that destroy tumor cells, virally-infected cells, and antibody-coated cells. Tetrabromobisphenol A (TBBPA) is used both as a reactive and as an additive flame retardant in a variety of materials and appears to contaminate the environment. TBBPA has been found in human blood samples and if it interferes with NK cell function, this could increase the risk of tumor development and/or viral infection. The present study examines the effects of exposure to various concentrations of TBBPA for 24 hr, 48 hr, and 6 days on the lytic function, tumor-target-binding function, and ATP levels of NK cells. These same parameters were also monitored in NK cells that were exposed to TBBPA for 1 h followed by 24 hr, 48 hr, and 6 days in TBBPA-free media. A 24-h exposure of NK cells to 5 microM TBBPA caused a >95% decrease in NK lytic function, a 70% decrease in binding function, and a 34% decrease in ATP levels in NK cells. Exposure to 2.5 microM TBBPA for 24 h decreased lytic function by 76%, binding function by 20%, and had no effect on ATP levels. Exposure of NK cells to 5 microM TBBPA for 1 h followed by 24 h in TBBPA-free media caused a progressive and persistent loss of lytic function (41%) while not affecting either binding ability or ATP levels. The results indicate that TBBPA exposures decrease the lytic function of human NK cells and that an initial brief (1 hr) exposure can cause a progressive loss of function. In addition, the data also indicate that TBBPA-induced loss of NK lytic function can occur at a concentration of TBBPA that does not affect target-binding ability and ATP levels of NK cells.
人类自然杀伤 (NK) 细胞是破坏肿瘤细胞、病毒感染细胞和抗体包被细胞的淋巴细胞。四溴双酚 A(TBBPA)既作为反应性阻燃剂,也作为添加剂阻燃剂用于各种材料中,似乎会污染环境。已在人类血液样本中发现 TBBPA,如果它干扰 NK 细胞功能,这可能会增加肿瘤发展和/或病毒感染的风险。本研究检查了暴露于不同浓度的 TBBPA 24 小时、48 小时和 6 天对 NK 细胞的裂解功能、肿瘤靶向结合功能和 ATP 水平的影响。还监测了 NK 细胞在暴露于 TBBPA 1 小时后,然后在不含 TBBPA 的培养基中培养 24 小时、48 小时和 6 天的相同参数。NK 细胞暴露于 5μM TBBPA 24 小时导致 NK 裂解功能降低超过 95%,结合功能降低 70%,ATP 水平降低 34%。暴露于 2.5μM TBBPA 24 小时使裂解功能降低 76%,结合功能降低 20%,对 ATP 水平没有影响。NK 细胞暴露于 5μM TBBPA 1 小时,然后在不含 TBBPA 的培养基中培养 24 小时,导致裂解功能逐渐和持续丧失(41%),而不影响结合能力或 ATP 水平。结果表明,TBBPA 暴露会降低人 NK 细胞的裂解功能,而最初的短暂(1 小时)暴露会导致功能逐渐丧失。此外,数据还表明,TBBPA 诱导的 NK 裂解功能丧失可发生在不影响 NK 细胞靶结合能力和 ATP 水平的 TBBPA 浓度下。