Complete transformation of embryonal rat fibroblasts by polyomavirus occurs during passage in vitro

Exp Cell Res. 1990 Mar;187(1):143-9. doi: 10.1016/0014-4827(90)90128-w.

Abstract

The tumorigenicity of secondary rat embryo fibroblasts transfected with a plasmid harboring a replication origin-defective polyomavirus was found to increase during in vitro propagation. Thus, polyomavirus-transfected cells were found to be more than 10,000-fold more tumorigenic when injected into syngenic rats at 3 months after transfection compared to those injected at an earlier time point. Furthermore, most clones of polyomavirus-transfected cells did not grow in semisolid medium at 52 days after transfection but did grow at 95 days. Addition of glucocorticoid hormones, but not of 25% fetal calf serum, to the growth medium of the early passage cells resulted in limited anchorage-independent growth. An altered level of expression of a number of proteins was found in cells analyzed at different times after transfection. Notably, the expression of a component of the actin filament system, tropomyosin 2, was shown to decrease during growth in vitro. The development of a more fully transformed phenotype at late passages correlated with loss of the requirement for large T-antigen for growth. Thus, cells transfected with a polyomavirus mutant encoding a thermolabile large T-antigen did not grow at the restrictive temperature at 6 weeks after transfection, but grew well at 5 months after transfection. We suggest that these phenomena may be explained by assuming that establishment of rodent fibroblasts, and thereby sensitivity to transformation by middle T-antigen, is not an immediate consequence of expression of large T-antigen but occurs after a period of growth in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division
  • Cell Transformation, Neoplastic*
  • Cells, Cultured
  • Clone Cells
  • DNA Replication
  • Electrophoresis, Gel, Two-Dimensional
  • Embryo, Mammalian
  • Fibroblasts / cytology
  • Genes, Viral
  • Genes, ras
  • Methionine / metabolism
  • Plasmids
  • Polyomavirus / genetics*
  • Protein Biosynthesis
  • Proteins / isolation & purification
  • Rats
  • Thymidine / metabolism
  • Transfection

Substances

  • Proteins
  • Methionine
  • Thymidine