Odewumi Caroline O, Fils-Aime Shiela, Badisa Veera L D, Latinwo Lekan M, Ruden Michael L, Ikediobi Christopher, Badisa Ramesh B
Departments of Biology, Florida A&M University, Tallahassee, Florida, USA.
Departments of Chemistry, Florida A&M University, Tallahassee, Florida, USA.
Environ Toxicol. 2015 May-Jun;30(6):704-11. doi: 10.1002/tox.21948. Epub 2014 Jan 13.
Cadmium is commercially profitable element, but it causes toxicity in humans and animals leading to diseases in various organs. The main route of cadmium exposure to humans is through inhalation. Lungs respond to insult through secretion of cytokines. In this study, the chemoprotective effect of monoisoamyl 2, 3-dimercaptosuccinate (MiADMS) was evaluated on viability and cytokines expression in CdCl2 treated human lung A549 cells by cytokine array. Cells were treated with 0, 50, 75, and 100 µM CdCl2 alone, 300 µM MiADMS alone, and co-treated with 300 µM MiADMS and 75 µM CdCl2 for 24 h. The viability was measured by crystal violet dye. The level of cytokines in the cells' lysate and cell culture medium was measured using Ray Biotech's Human Cytokine Array 6 in control cells, 75 µM CdCl2 alone and MiADMS co-treated cells. Array results were validated by ELISA kit. The CdCl2 caused a dose dependent decrease in cell viability, while MiADMS co-treatment resulted in a significant increase in viability of CdCl2 treated cells. Morphology of the cells treated with CdCl2 was destroyed, while MiADMS restored the lost shape in CdCl2 treated cells. In addition, the cells co-treated with MiADMS and CdCl2 showed modulation of cytokines expression in comparison to the CdCl2 alone treated cells. The ELISA results showed the similar pattern of cytokine expression as Human Cytokine Array and validated the array results. These results clearly show the chemoprotective effect of MiADMS and suggest that MiADMS can be used as antidote at moderate dose against CdCl2 toxicity.
镉是一种具有商业价值的元素,但它会对人类和动物产生毒性,导致各个器官出现疾病。人类接触镉的主要途径是通过吸入。肺部通过分泌细胞因子来应对损伤。在本研究中,通过细胞因子阵列评估了单异戊基2,3-二巯基丁二酸(MiADMS)对氯化镉处理的人肺A549细胞活力和细胞因子表达的化学保护作用。细胞分别用0、50、75和100 μM氯化镉单独处理、300 μM MiADMS单独处理以及300 μM MiADMS与75 μM氯化镉共同处理24小时。通过结晶紫染料测量细胞活力。使用Ray Biotech的人类细胞因子阵列6检测对照细胞、单独75 μM氯化镉处理的细胞以及MiADMS共同处理的细胞中细胞裂解液和细胞培养基中的细胞因子水平。阵列结果通过ELISA试剂盒进行验证。氯化镉导致细胞活力呈剂量依赖性下降,而MiADMS共同处理导致氯化镉处理的细胞活力显著增加。氯化镉处理的细胞形态被破坏,而MiADMS恢复了氯化镉处理细胞失去的形态。此外,与单独氯化镉处理的细胞相比,MiADMS和氯化镉共同处理的细胞显示出细胞因子表达的调节。ELISA结果显示出与人类细胞因子阵列相似的细胞因子表达模式,并验证了阵列结果。这些结果清楚地表明了MiADMS的化学保护作用,并表明MiADMS可以作为中等剂量的解毒剂来对抗氯化镉毒性。