Expression of NK cells activation receptors after occupational exposure to toxics

• Published in: Immunology letters Vol. 118; no. 2; pp. 125 - 131
• Main Authors: De Celis, Ruth, Feria-Velasco, Alfredo, Bravo-Cuellar, Alejandro, Hicks-Gómez, Juan José, García-Iglesias, Trinidad, Preciado-Martínez, Verónica, Muñoz-Islas, Laura, González-Unzaga, Marco
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 2008
• Subjects: Activation receptors; Allergy and Immunology; Immune response; NK cells; Occupational exposure; Mexico, Jalisco; cell surface receptors for the Fc portion of IgG; zetta chain of cluster differentiation; KARAP/ DAP12; MHC; major histocompatibility complex; Occupational exposure; gas chromatography; immunoreceptor tyrosine-based activation motifs; natural killer; CD3ζ; GC; MICA; major histocompatibility complex class I related gene B; FcRγ; major histocompatibility complex class I related gene A; MICB; BMI; NK cells; Immune response; body mass index; Activation receptors; killer cell activing receptor associated protein; natural cytotoxic receptors; NCRs; ITAM; NK
• ISSN: 0165-2478; 1879-0542
• DOI: 10.1016/j.imlet.2008.03.010

Abstract The expression of NK cells activation receptors was assessed by comparative study of two groups of women workers at a chemical reagents factory, located in Zapopan, Jalisco, Mexico. Twenty of them were exposed to environmental toxics identified and quantified by gas chromatography, and 20 women unexposed to toxic substances. The expression of the surface markers CD56+ and CD3+, and of the activation receptors and co-receptors on NK cells was quantified by flow cytometry. To assess the cellular damage produced by chronic exposure to the toxics, the thiobarbituric acid reacting substances (TBARS) generated and the total plasma antioxidizing capacity (TPAC) were quantified in both groups. The exposed women had been exposed at least to 12 volatile toxic compounds, benzene, benz(a)pyrene, ethylbenzene, dimethylbenz(a)anthracene, xylene, toluene, styrene, chloroform, formaldehyde, iodine, chlorine and fluorine. Significant difference between the two groups was in the proportion of CD3 lymphocytes, 72.7 ± 10.3% in the unexposed women versus 66.8 ± 7.9% in the exposed group ( p < 0.05). The density of expression of NKG2D and NKp30 receptors was significantly higher in the unexposed women compared to the exposed group: NKG2D were 31.3 ± 6.3 and NKp30 were 9.5 ± 5.2 in the unexposed women and 5.14 ± 2.9 ( p < 0.01) and 4.6 ± 1.9 ( p < 0.05), respectively in the exposed women. No statistically significant differences were found in the expression of NKp80, NKp46 and 2B4 receptors. The concentration of TBARS was lower in women from the unexposed group than the corresponding data from women of the exposed group. However, no significant difference was observed in TPAC between the two groups studied. The results of this preliminary study suggest that from the five activation receptors and co-receptors of NK cells evaluated (NKp30, NKp46, NKp80, NKG2D and 2B4), only NKp30 and NKG2D receptor expression was diminished in women exposed to toxics when compared with data from unexposed women. These results suggest that the occupational exposure to mixture of toxics is one of the important factors in the diminution of the NK cell receptor expression.