Literature DB >> 12902148

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

Sabah O Odman-Ghazi1, Frank Hatcher, Margaret M Whalen.   

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.

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Year:  2003        PMID: 12902148     DOI: 10.1016/s0009-2797(03)00069-3

Source DB:  PubMed          Journal:  Chem Biol Interact        ISSN: 0009-2797            Impact factor:   5.192


  13 in total

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2.  Dibutyltin activates MAP kinases in human natural killer cells, in vitro.

Authors:  Sabah O Odman-Ghazi; Abraham Abraha; Erica Taylor Isom; Margaret M Whalen
Journal:  Cell Biol Toxicol       Date:  2010-03-24       Impact factor: 6.691

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4.  Tetrabromobisphenol A decreases cell-surface proteins involved in human natural killer (NK) cell-dependent target cell lysis.

Authors:  Tasia Hurd; Margaret M Whalen
Journal:  J Immunotoxicol       Date:  2011-05-31       Impact factor: 3.000

5.  Secretion of interferon gamma from human immune cells is altered by exposure to tributyltin and dibutyltin.

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6.  Effects of butyltin exposures on MAP kinase-dependent transcription regulators in human natural killer cells.

Authors:  Rachel J Person; Margaret M Whalen
Journal:  Toxicol Mech Methods       Date:  2010-06       Impact factor: 2.987

7.  Effects of ziram on tumor-cell-binding capacity, cell-surface marker expression, and ATP levels of human natural killer cells.

Authors:  Thyneice R Taylor; Margaret M Whalen
Journal:  Cell Biol Toxicol       Date:  2008-08-01       Impact factor: 6.691

8.  Hexabromocyclododecane decreases tumor-cell-binding capacity and cell-surface protein expression of human natural killer cells.

Authors:  Natasha C Hinkson; Margaret M Whalen
Journal:  J Appl Toxicol       Date:  2010-05       Impact factor: 3.446

9.  Tributyltin and dibutyltin alter secretion of tumor necrosis factor alpha from human natural killer cells and a mixture of T cells and natural killer cells.

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Journal:  J Appl Toxicol       Date:  2012-10-10       Impact factor: 3.446

10.  Pentachlorophenol decreases tumor-cell-binding capacity and cell-surface protein expression of human natural killer cells.

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Journal:  J Appl Toxicol       Date:  2012-08       Impact factor: 3.446

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