The Role of Chemical Inhibition of Gap-Junctional Intercellular Communication in Toxicology

Abstract

Progress during the first 12 months of this grant has progressed on all six specific aims, namely to study the basic mechanisms by which toxic chemicals block cell-cell communication; role of oncogenes in down-regulating gap junctional intercellular communication (GJIC); how protein kinase C enzyme, after activated by chemicals, down regulates GJIC; validate known toxic chemicals' ability to block GJIC in new human cell lines; isolate gap junction antibodies to characterize and study how gap junctions are regulated; and to isolate and characterize gap junction mutants. Several experimental, theoretical and review articles have been submitted. Presented research at recent international meetings and several national meetings. Gap junctions; Cell communication; Tumor promoters; Teratogens; Neurotoxins; Protein kinase C; Chemical toxicity; Biochemistry; Carcinogens.

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Document Details

Document Type
Technical Report
Publication Date
Mar 31, 1990
Accession Number
ADA221480

Entities

People

  • James E. Trosko

Organizations

  • Michigan State University

Tags

DTIC Thesaurus Topics

  • Antibodies
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Diseases And Disorders
  • Epithelial Cells
  • Growth Factors
  • Human Development
  • Inhibition
  • Intercellular Junctions
  • Michigan
  • Modulation
  • Neoplasms
  • Risk Analysis
  • Toxicity
  • Toxicology
  • Universities

Fields of Study

  • Biology

Readers

  • Academic Conference Management
  • Molecular Biology and Genetics
  • Toxicology/Environmental Toxicology