We will determine whether two lymphocyte functional assays, the B-cell colony forming (B-CFC) assay and a variant of the T-cell mixed lymphocyte culture (MLC) assay, can be used as sensitive indicators of exposure to low concentrations of compound commonly found in toxic waste. In a series of prior studies, the immunotoxic effects of inhaled benzene were assessed using seven different lymphocyte functional assays. In order to make the experiments as relevant as possible, the assays were performed either on intact mice exposed to benzene via inhalation or on lymphocytes isolate from such mice. Marked disruptions of all assays were observed, but the B-CFC and MLC exhibited by far the most sensitivity to the benzene exposures. Marked changes in the responses of these latter assays were observed after relatively brief exposures to low concentrations of benzene. The reaction of electrophilic intermediates or metabolites with membrane bound sulfhydryl groups is believed to be the common pathway by which exogenous contaminants disrupt the immune response. Benzene is known to be metabolized to quinones which react with sulfhydryl groups. Unmetabolized benzene does not react with sulfhydryl groups. The B-CFC and MLC assays, therefore, were sufficiently sensitive to be markedly disrupted by presumably very low levels in vivo produced electrophilic benzene metabolites. It is likely that other toxicants which produce electrophilic intermediates will also markedly disrupt the lymphocyte functions measured by these assays. This is the hypothesis to be tested. We will evaluate the B-CFC and MLC assays by employing protocols that investigate dose/response, time course response, persistence after exposure and structure activity relationships. Compounds typical of those commonly found in toxic waste will be delivered to mice and rats by routes of exposure that are relevant to human exposure to toxic waste. The compounds to be studied are: the aromatic hydrocarbons benzene, toluene, and xylenes; the chlorinated hydrocarbons methylene chloride, chloroform, and carbon tetrachloride; the mixture of chlorinated aromatic hydrocarbons aroclor 1254; and the metal salts nickel acetate, potassium chromate, and methylmercuric chloride.

Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1991
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
Sutherland, J E; Zhitkovich, A; Kluz, T et al. (2000) Rats retain chromium in tissues following chronic ingestion of drinking water containing hexavalent chromium. Biol Trace Elem Res 74:41-53
Corti, M; Snyder, C A (1998) Gender- and age-specific cytotoxic susceptibility to benzene metabolites in vitro. Toxicol Sci 41:42-8
Salnikow, K; Wang, S; Costa, M (1997) Induction of activating transcription factor 1 by nickel and its role as a negative regulator of thrombospondin I gene expression. Cancer Res 57:5060-6
Klein, C B; Costa, M (1997) DNA methylation, heterochromatin and epigenetic carcinogens. Mutat Res 386:163-80
Gong, Z; Evans, H L (1997) Effect of chelation with meso-dimercaptosuccinic acid (DMSA) before and after the appearance of lead-induced neurotoxicity in the rat. Toxicol Appl Pharmacol 144:205-14
Dowjat, W K; Kharatishvili, M; Costa, M (1996) DNA and RNA strand scission by copper, zinc and manganese superoxide dismutases. Biometals 9:327-35
Snyder, C A; Udasin, I; Waterman, S J et al. (1996) Reduced IL-6 levels among individuals in Hudson County, New Jersey, an area contaminated with chromium. Arch Environ Health 51:26-8
Corti, M; Snyder, C A (1996) Influences of gender, development, pregnancy and ethanol consumption on the hematotoxicity of inhaled 10 ppm benzene. Arch Toxicol 70:209-17
Garte, S J; Trachman, J; Crofts, F et al. (1996) Distribution of composite CYP1A1 genotypes in Africans, African-Americans and Caucasians. Hum Hered 46:121-7
Dowjat, W K; Huang, X; Cosentino, S et al. (1996) Peroxidase deficiency of nickel-transformed hamster cells correlates with their increased resistance to cytotoxicity of peroxides. Biometals 9:151-6

Showing the most recent 10 out of 106 publications