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Quantitation of simian virus 40 T-antigen correlated with the cell cycle of permissive and non-permissive cells.

Abstract
These studies examined cell cycle progression and quantitative changes in T-antigen following infection by SV40. Single cells were assayed by multiparameter flow cytometric analysis (FCM) for DNA content and T-antigen expression. Conditions were used which permitted permissive, semi-permissive, and non-permissive cells to be monitored through two rounds of DNA synthesis induced by SV40. The permissive cells included the monkey kidney cell lines; CV-1, Vero and BSC-1 and the COS-1 and COS-7 which are CV-1 cells transformed with an origin defective SV40. The non-permissive cell strains included mouse embryo fibroblasts, Chinese hamster fibroblasts, and IMR-90, a human diploid fibroblast. Cell types differed in the maximal amount of T-antigen expressed per cell. Additionally, all cell types expressed a limited quantity of T-antigen for each cell cycle phase and the quantity increased in each successive phase. The level in each phase was increased only two-fold when 100 times more virus was used. Thus, for an infected population the quantity of T-antigen was dependent on cell cycle distribution. High levels of T-antigen were not required for permissive infection; however, permissive cells were distinguished from non-permissive cells by the G2 levels. Permissive G2 cells had more than double the T-antigen content expressed in G1, while nonpermissive G2 cells had less than a two-fold increase over G1 levels. The appearance of cells with tetraploid DNA content and the failure to undergo mitosis correlated to the higher T-antigen levels in the G2 of the permissive cells. Two other strains of SV40, 776, and VA45 exhibit similar values for T-antigen expression and movement into tetraploid DNA content. This study establishes the levels of T-antigen correlated to the cell cycle and cell type.
AuthorsJ M Lehman, T D Friedrich, J Laffin
JournalCytometry (Cytometry) Vol. 14 Issue 4 Pg. 401-10 ( 1993) ISSN: 0196-4763 [Print] United States
PMID8390342 (Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antigens, Polyomavirus Transforming
  • DNA
Topics
  • Animals
  • Antigens, Polyomavirus Transforming (analysis, biosynthesis)
  • Cell Cycle
  • Cell Line
  • Cell Transformation, Viral
  • Chlorocebus aethiops
  • Cricetinae
  • Cricetulus
  • DNA (analysis)
  • Defective Viruses (physiology)
  • Fibroblasts (microbiology)
  • Flow Cytometry
  • Humans
  • Mice (embryology)
  • Simian virus 40 (immunology, physiology)
  • Species Specificity
  • Virus Replication

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