Omara F O, Flipo D, Brochu C, Denizeau F, Brousseau P, Potworowski E F, Fournier M
TOXEN, UQAM, Montréal, Québec, Canada.
J Toxicol Environ Health A. 1998 Aug 7;54(7):561-77. doi: 10.1080/009841098158700.
Rat splenocyte mixed leukocyte reaction (MLR), splenic natural killer (NK) cell activity, and phagocytic activities of splenic, peritoneal, and peripheral blood leukocytes (PBLs) were evaluated in vitro to determine the immunotoxicity of mixtures containing low levels of methylmercury (MeHg), polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and Aroclor polychlorinated biphenyls (PCBs). The mixtures were based on the concentrations of the chemicals in fish flesh. Leukocytes from male Fischer rats were exposed to MeHg (0.1-2 microg/ml), PCDD/PCDF mixtures (1-15 pg/ml) of three PCDDs (2,3,7,8-tetrachlorodibenzo-p-dioxin, 1,2,3,7,8-pentachlorodibenzo-p-dioxin, and 1,2,3,4,7,8-hexachlorodibenzo-p-dioxin) and two PCDFs (2,3,7,8-tetrachlorodibenzofuran and 1,2,3,7,8-pentachlorodibenzofuran), three Aroclor PCB (Aroclor 1242, 1254, and 1260) mixtures (0.01-0.5 microg/ml), or combinations of MeHg/PCB/PCDD/PCDF mixtures for 24 or 72 h before immunological assays. Phagocytosis and NK cell cytotoxicity were evaluated with a flow cytometer, and MLR of Fischer rat responder splenocytes cultured with mitomycin C-treated Long-Evans splenocytes by [3H]thymidine uptake. Exposure to MeHg (2 microg/ml) alone or with PCB/ PCDD/PCDF resulted in significant cytolethality in rat splenocytes, peritoneal leukocytes, and PBLs at 24 h exposure. Treatment with Aroclor PCB mixtures, PCDD/PCDF mixtures, 0.1 microg MeHg/ml (noncytolethal), or PCB/PCDD/PCDF mixtures with 0.1 microg MeHg/ml caused no suppression of splenocyte MLR response, splenic NK cell-mediated lysis of Yac-l cells, or phagocytosis of fluorescent beads by splenic, peritoneal, and peripheral blood phagocytic cells. The results indicate that in vitro exposure of rat leukocytes to low levels of MeHg, Aroclor PCB mixtures, PCDD/PCDF mixtures, or MeHg/PCB/PCDD/PCDF mixtures had no suppressive effects on the immune functions assayed, and thus produced no additive immunotoxicity. However, in order to predict the potential risk of these chemical mixtures to the human immune system, in vivo animal studies with blood (tissue) levels compatible with the levels of MeHg, PCBs, and PCDDs/PCDFs in exposed human populations should be evaluated.
在体外评估大鼠脾细胞混合白细胞反应(MLR)、脾脏自然杀伤(NK)细胞活性以及脾脏、腹膜和外周血白细胞(PBL)的吞噬活性,以确定含有低水平甲基汞(MeHg)、多氯二苯并 - p - 二恶英(PCDDs)、多氯二苯并呋喃(PCDFs)和氯丹多氯联苯(PCBs)的混合物的免疫毒性。这些混合物基于鱼肉中化学物质的浓度。在进行免疫测定前24或72小时,将雄性Fischer大鼠的白细胞暴露于MeHg(0.1 - 2微克/毫升)、三种PCDD(2,3,7,8 - 四氯二苯并 - p - 二恶英、1,2,3,7,8 - 五氯二苯并 - p - 二恶英和1,2,3,4,7,8 - 六氯二苯并 - p - 二恶英)和两种PCDF(2,3,7,8 - 四氯二苯并呋喃和1,2,3,7,8 - 五氯二苯并呋喃)的PCDD/PCDF混合物(1 - 15皮克/毫升)、三种氯丹PCB(氯丹1242、1254和1260)混合物(0.01 - 0.5微克/毫升)或MeHg/PCB/PCDD/PCDF混合物的组合中。用流式细胞仪评估吞噬作用和NK细胞细胞毒性,并用[³H]胸腺嘧啶核苷摄取法评估用丝裂霉素C处理的Long - Evans脾细胞培养Fischer大鼠反应性脾细胞的MLR。单独暴露于MeHg(2微克/毫升)或与PCB/PCDD/PCDF一起暴露24小时会导致大鼠脾细胞、腹膜白细胞和PBL中出现显著的细胞毒性。用氯丹PCB混合物、PCDD/PCDF混合物以及0.1微克MeHg/毫升(无细胞毒性)或含0.1微克MeHg/毫升的PCB/PCDD/PCDF混合物处理,不会抑制脾细胞MLR反应、脾脏NK细胞介导的对Yac - 1细胞的裂解或脾脏、腹膜和外周血吞噬细胞对荧光珠的吞噬作用。结果表明,大鼠白细胞在体外暴露于低水平的MeHg、氯丹PCB混合物、PCDD/PCDF混合物或MeHg/PCB/PCDD/PCDF混合物对所检测的免疫功能没有抑制作用,因此不会产生相加免疫毒性。然而,为了预测这些化学混合物对人类免疫系统的潜在风险,应评估与暴露人群中MeHg、PCBs和PCDDs/PCDFs水平相匹配的血液(组织)水平的体内动物研究。