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二丁基锡暴露的人自然杀伤细胞中功能相关细胞表面标志物的表达。

Expression of functionally relevant cell surface markers in dibutyltin-exposed human natural killer cells.

作者信息

Odman-Ghazi Sabah O, Hatcher Frank, Whalen Margaret M

机构信息

Department of Chemistry, Tennessee State University, 3500 John A Merritt Blvd, Nashville, TN 37209-1561, USA.

出版信息

Chem Biol Interact. 2003 Jul 25;146(1):1-18. doi: 10.1016/s0009-2797(03)00069-3.

Abstract

Butyltin (BT) compounds are known for their worldwide contamination. Dibutyltin (DBT) is used as a stabilizer in plastic products, and as a deworming agent in poultry. Poultry products have been shown to contain measurable levels of DBT. Drinking water has also been reported to contain BTs due to leaching from PVC pipes. We, and others, have found measurable levels of DBT in human blood. BTs appear to increase the risk of cancer and other viral infections in exposed individuals. In previous studies we have shown that the tumor killing function of natural killer (NK) lymphocytes was greatly diminished after as little as a 1 h exposure to DBT and the inhibition continued even after removal of the compound. We also showed that there was a significant decrease in NK cell lysis of K562 target cells after an exposure to 1.5 microM DBT for 24 h. This 24 h exposure also decreased the ability of NK cells to bind to tumor cells. Loss of binding function was not seen when NK cells were exposed to 5-10 microM DBT for 1 h. However, NK cells exposed to 5 microM DBT for 1 h and then incubated in DBT-free media for 24, 48, or 96 h, showed a significant loss of tumor-binding function within 24 h. The effects of DBT exposure on seven cell surface molecules that are involved in NK-cell interactions with target cells were investigated. The results indicated that the exposure of NK cells to 1.5 microM DBT for 24 h decreased the expression of CD2, CD11a, CD16, CD11c. There was no decrease in expression of any of the markers studied when NK cells were exposed to 5 microM DBT for 1 h, consistent with the fact that a 1-h exposure had no effect on the ability of NK cells to bind tumor cells. However, when NK cells were exposed to 5 microM DBT for 1 h followed by 24, 48 or 96 h incubations in DBT-free media there was decreased expression of several of the cells surface molecules with the most dramatic decreases being in CD16 and CD56.

摘要

丁基锡(BT)化合物因其在全球范围内的污染而闻名。二丁基锡(DBT)被用作塑料制品的稳定剂以及家禽的驱虫剂。已证明家禽产品中含有可测量水平的DBT。据报道,由于聚氯乙烯(PVC)管道的渗漏,饮用水中也含有丁基锡化合物。我们以及其他研究人员发现人体血液中存在可测量水平的DBT。丁基锡化合物似乎会增加接触者患癌症和其他病毒感染的风险。在先前的研究中,我们发现自然杀伤(NK)淋巴细胞在仅暴露于DBT 1小时后,其肿瘤杀伤功能就会大幅减弱,并且即使在去除该化合物后,这种抑制作用仍会持续。我们还表明,在暴露于1.5微摩尔/升DBT 24小时后,NK细胞对K562靶细胞的裂解作用显著降低。这种24小时的暴露还降低了NK细胞与肿瘤细胞结合的能力。当NK细胞暴露于5 - 10微摩尔/升DBT 1小时时,未观察到结合功能丧失。然而,NK细胞暴露于5微摩尔/升DBT 1小时,然后在不含DBT的培养基中孵育24、48或96小时,在24小时内就显示出肿瘤结合功能的显著丧失。研究了DBT暴露对参与NK细胞与靶细胞相互作用的七种细胞表面分子的影响。结果表明,NK细胞暴露于1.5微摩尔/升DBT 24小时会降低CD2、CD11a、CD16、CD11c的表达。当NK细胞暴露于5微摩尔/升DBT 1小时时,所研究的任何标志物的表达均未降低,这与1小时的暴露对NK细胞结合肿瘤细胞的能力没有影响这一事实一致。然而,当NK细胞暴露于5微摩尔/升DBT 1小时,随后在不含DBT的培养基中孵育24、48或96小时时,几种细胞表面分子的表达降低,其中CD16和CD56的降低最为显著。

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