Macromolecular metabolism of a differentiated rat keratinocyte culture system following exposure to sulfur mustard

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Abstract
A method for producing a stratified, squamous epithelium in vitro by cultivating rat keratinocytes on nylon membranes has been developed in this laboratory. This epidermal‐like culture is being used to obtain a better understanding of the mechanism of skin vesication after topical exposure to the sulfur mustard bis(beta‐chloroethyl) sulfide (BCES) dissolved in a selected solvent. Radiolabeled macromolec‐ular precursors (thymidine, uridine, and leucine) have been used to study the effect of BCES on the synthesis of DNA, RNA, and protein, respectively, after topical exposure to the mustard at concentrations of 0.01–500 nmol/cm2 dissolved in 70% dimethyl sulfoxide (DMSO). From these and other studies it has been determined that exposure to even the low concentration of 0.01 nmol BCES/cm2 for 30 min results in significant inhibition of [3H]thymidine incorporation, although complete recovery occurs by 24 h. Significant inhibition of [3H]uridine and [14C]Ieucine incorporation is observed only after exposure to much higher concentrations of BCES (10–500 nmol/cm2). This suggests a very early lesion in macromolecular metabolism with DNA being the primary target.