Fugère N, Brousseau P, Krzystyniak K, Coderre D, Fournier M
Département des Sciences Biologiques, and TOXEN, Université du Qúebec à Montréal, Canada.
Toxicology. 1996 May 17;109(2-3):157-66. doi: 10.1016/0300-483x(96)03315-x.
Cell viability and phagocytic activity of coelomocytes from the gastrointestinal tract of Lumbricus terrestris were examined by flow cytometry after in vitro exposure to heavy metals. Control coelomocytes were incubated for 18 h at 15 degrees C, 5% CO2, in Ca(++)-containing LBSS medium with 10(-4)-10(-9) M mercury chloride, methylmercury, cadmium chloride, zinc chloride, lead chloride or lead acetate. Heterogeneity of coelomocyte population was demonstrated by forward scatter (FSC) analysis and cytometric profile showing two different populations of type I/small (60%) and type-II/large (40%) cells. Exposure to either form of Hg, Cd and Zn was relatively highly toxic and affected both cell viability and phagocytosis, whereas Pb was relatively well tolerated by the coelomocytes. A fraction of cells within large coelomocyte population was exceptionally sensitive to the Hg-induced cytotoxicity, which did not affect, however, the relative phagocytic activity of the remaining cells. Overall, at least three different patterns of metal-specific toxicity, affecting both viability and phagocytic functions of earthworm coelomocytes, were confirmed in our in vitro studies. Further characterisation of both the target cells from heterogeneous coelomocyte population and the specific interaction of target cell-xenobiotic can possibly reduce biomonitoring problems in earthworm toxicology and immunotoxicology.
在体外暴露于重金属后,通过流式细胞术检测了赤子爱胜蚓胃肠道中体腔细胞的细胞活力和吞噬活性。将对照体腔细胞在含Ca(++)的LBSS培养基中,于15℃、5%二氧化碳条件下孵育18小时,培养基中含有10(-4)-10(-9)M的氯化汞、甲基汞、氯化镉、氯化锌、氯化铅或醋酸铅。通过前向散射(FSC)分析和细胞图谱显示体腔细胞群体的异质性,表明存在两种不同类型的细胞,即I型/小细胞(60%)和II型/大细胞(40%)。暴露于任何一种形式的汞、镉和锌都具有相对较高的毒性,会影响细胞活力和吞噬作用,而铅相对而言体腔细胞耐受性较好。大的体腔细胞群体中的一部分细胞对汞诱导的细胞毒性异常敏感,然而这并不影响其余细胞的相对吞噬活性。总体而言,在我们的体外研究中证实了至少三种不同的金属特异性毒性模式,它们影响蚯蚓体腔细胞的活力和吞噬功能。对异质体腔细胞群体中的靶细胞以及靶细胞与异生物质的特异性相互作用进行进一步表征,可能会减少蚯蚓毒理学和免疫毒理学中的生物监测问题。