Powell Jeralyn J, Davis McLisa V, Whalen Margaret M
Department of Biological Sciences, Tennessee State University, Nashville, Tennessee 37209, USA.
Drug Chem Toxicol. 2009;32(1):9-16. doi: 10.1080/01480540802416000.
This study investigated whether reduced glutathione (GSH) was able to alter the negative effects of tributyltin (TBT) or dibutyltin (DBT) on the lytic function of human natural killer (NK) cells. NK cells are an initial immune defense against the development of tumors or viral infections. TBT and DBT are widespread environmental contaminants, due to their various industrial applications. Both TBT and DBT have been shown to decrease the ability of NK cells to lyse tumor cells (lytic function). The results indicated that the presence of GSH during the exposure of NK cells to TBT or DBT diminished the negative effect of the butyltin on the lytic function of NK cells. This suggests that the interaction of TBT and DBT with functionally relevant sulfhydryl groups in NK cells may be part of the mechanism by which they decrease NK lytic function.
本研究调查了还原型谷胱甘肽(GSH)是否能够改变三丁基锡(TBT)或二丁基锡(DBT)对人自然杀伤(NK)细胞裂解功能的负面影响。NK细胞是针对肿瘤发生或病毒感染的初始免疫防御。由于其在各种工业中的应用,TBT和DBT是广泛存在的环境污染物。TBT和DBT均已被证明会降低NK细胞裂解肿瘤细胞的能力(裂解功能)。结果表明,在NK细胞暴露于TBT或DBT期间存在GSH可减轻丁基锡对NK细胞裂解功能的负面影响。这表明TBT和DBT与NK细胞中功能相关的巯基的相互作用可能是它们降低NK裂解功能的机制的一部分。