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Uptake and nature of the intracellular binding of cyclosporin A in a murine thymoma cell line, BW5147.

Abstract
In a survey of malignant cell lines including a variety of leukemias and lymphomas, BW5147, a T lymphoma from the spontaneous virus-associated thymoma in AKR mice, was found to be the most sensitive to growth inhibition by cyclosporin A (Cs A). Inhibition of growth was cell cycle phase-independent and inhibition of macromolecular precursor uptake was relatively nonspecific. Uptake of radiolabeled Cs A by these cells was characterized by two components: one that appeared saturable at low drug concentrations (0.03 to 1.0 microgram/ml), and another that was nonsaturable at higher drug concentrations (1.0 microgram/ml or higher). Most of the drug concentrated by cells (70 to 80%) was located in the cytosol (100,000 X G supernatant of lysed cells). The apparent m.w. of the drug-macromolecule complex was 15,000 to 20,000 as determined by m.w. exclusion columns. This complex could also be formed by adding drug to cytosol prepared from unexposed cells. The low m.w. complex migrated on a preparative isoelectric focusing column to form two peaks with isoelectric points of 6.8 and 8.5. A method was developed to assay for the binding component, and a sequence of m.w. exclusion columns and isoelectric focusing was used to effect partial purification of the Cs A binding component.
AuthorsM P Merker, M M Merker, R E Handschumacher
JournalJournal of immunology (Baltimore, Md. : 1950) (J Immunol) Vol. 132 Issue 6 Pg. 3064-70 (Jun 1984) ISSN: 0022-1767 [Print] United States
PMID6609967 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Cyclosporins
  • Growth Inhibitors
  • Receptors, Immunologic
  • cyclosporin receptor
Topics
  • Animals
  • Cell Line
  • Cell Transformation, Neoplastic (drug effects, metabolism)
  • Cyclosporins (metabolism, pharmacology)
  • Cytosol (metabolism)
  • Dose-Response Relationship, Drug
  • Growth Inhibitors (pharmacology)
  • Lymphoma (drug therapy, metabolism)
  • Mice
  • Mice, Inbred AKR
  • Receptors, Immunologic (isolation & purification, metabolism)
  • T-Lymphocytes (drug effects, metabolism)
  • Thymoma (drug therapy, metabolism)

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