Retroviral transduction of alveolar bone cells with a temperature-sensitive SV40 large T antigen.

Vehid Salih, Jonathan C. Knowles, Michael J. O'Hare, Irwin Olsen*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

We have transduced adult human alveolar bone (AB) cells with a gene construct encoding a temperature-sensitive mutation of the SV40 large T antigen (tsT). Such cells divided rapidly, for more than 50 passages thus far, at a permissive low temperature (34.5 degrees C), comparable to the non-transduced parental cells at 37 degrees C. However, the tsT-transduced AB cells failed to grow at a non-permissive high temperature (39 degrees C) at which the T antigen is inactivated. Nevertheless, the cells formed mineralised nodules in vitro at both the low and high temperatures. Flow cytometry analysis showed that the transduced cells cultured at 34.5 degrees C, like the parental cells at 37 degrees C, were smaller and less granular than the transduced cells incubated at 39 degrees C. Moreover, the transduced cells grown at 34.5 degrees C were also found to express bone sialoprotein, osteopontin and type I collagen at levels similar to those of the parental cells at 37 degrees C, although osteonectin and fibronectin were down-regulated. When the transduced cells were incubated at 39 degrees C, the expression of all antigens was up-regulated, particularly osteonectin. Thus, we have obtained long-term cultures of tsT-transduced AB cells whose growth is temperature-dependent and which express certain features characteristic of bone-derived cells.
Original languageEnglish
Pages (from-to)371-376
Number of pages0
JournalCell Tissue Res
Volume304
Issue number3
DOIs
Publication statusPublished - Jun 2001

Keywords

  • Antigens
  • Polyomavirus Transforming
  • Biomarkers
  • Cell Division
  • Cell Line
  • Cell Size
  • Cell Transformation
  • Viral
  • Cytoplasmic Granules
  • Extracellular Matrix Proteins
  • Flow Cytometry
  • Hot Temperature
  • Humans
  • Kinetics
  • Mutation
  • Osteoblasts
  • Retroviridae
  • Sialoglycoproteins
  • Staining and Labeling
  • Tooth Socket
  • Transduction
  • Genetic

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