Chemical Blistering: Cellular and Macromolecular Components.

Abstract

The mission of this project was to determine the cellular and molecular lesions associated with cutaneous vesication from bis(2-chloroethyl)sulfide (BCES). Cultures of keratinocytes were used to focus attention on the direct interactions between the mustard and its epidermal targets. The technical objectives included confirming that DNA was the primary molecular target of BCES in human epidermal keratinocytes, identifying and quantifying BCES- mediated DNA-adducts in relation to dose, determining why epidermal basal cells are more susceptible to BCES than differentiated cells, and investigating the possible role of informational error in DNA in the cytopathogenic process. Data generated in the project suggest that (a) DNA is the primary epidermal target of BCES, and the fidelity of DNA repair governs survival of the germinative population, and (b)BCES causes a decrease in the germinative population by cellular differentiation, as indicated by the appearance of mature keratin protein, as well as necrosis.

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Document Details

Document Type
Technical Report
Publication Date
Oct 31, 1994
Accession Number
ADA294612

Entities

People

  • I. A. Bernstein

Organizations

  • University of Michigan

Tags

DTIC Thesaurus Topics

  • Alcohols
  • Cell Physiological Processes
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Chlorides
  • Deoxyribonucleic Acids
  • Liquid Chromatography
  • Mustard Agents
  • Necrosis
  • Nucleic Acids
  • Organic Chemistry
  • Pathologic Processes
  • Programmed Cell Death
  • Proteins

Fields of Study

  • Medicine

Readers

  • Molecular Genetics
  • Small Business Innovation Research Program (SBIR) EDI Research and Innovation.
  • Toxicology/Environmental Toxicology

Technology Areas

  • Biotechnology