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Partial reversion of conditional transformation correlates with a decrease in the sensitivity of rat cells to killing
N Salome1, B van Hille, M Geuskens
1Laboratoire d'Oncologie Moléculaire, Institut National de la Santé et de la Recherche Médicale U186, France.
Abstract:
The cytolytic effect of the autonomous parvovirus minute virus of mice, prototype strain (MVMp), was studied in cultures of ts 339/NRK rat cells that display a temperature-sensitive transformed phenotype as a result of their transformation with a Rous sarcoma virus strain matured in the v-src oncogene. A shift from restrictive (39.5 degrees C) to permissive (34.5 degrees C) temperature was associated with a marked sensitization of these cells to killing by MVMp. In contrast, ts 339/NRK cell derivatives supertransformed with a wild-type src oncogene were sensitive to MVMp at both temperatures, suggesting that the expression of a functional oncogene product may determine, at least in part, the extent of the parvoviral cytopathic effect. Although ts 339/NRK cells were quite resistant to parvoviral attack at 39.5 degrees C, they were similarly proficient in MVMp uptake, viral DNA and protein synthesis, and infectious particle production at both permissive and restrictive temperatures. Consistently, electron microscopic examination of infected ts 339/NRK cultures incubated at 39.5 degrees C revealed the presence, in the majority of the cells, of numerous full and empty virions that were predominantly located in autophagic-type vacuoles. Thus, in this system, the reversion of transformed and MVMp-sensitive phenotypes appears to correlate with the setting up of a noncytocidal mode of parvovirus production. These results raise the possibility that the physiological state of host cells may affect their susceptibility to parvoviruses by modulating not only their capacity for virus replication but also cellular processes controlling the cytopathic effect of viral products.
Insights
Minute virus of mice (MVMp) showed temperature-dependent killing of transformed rat cells. Cell transformation and oncogene expression influence MVMp
Area of Science:
- Virology
- Cell Biology
- Oncology
Background:
- Minute virus of mice (MVMp) is an autonomous parvovirus.
- Temperature-sensitive (ts) 339/NRK rat cells exhibit a transformed phenotype regulated by temperature.
- The v-src oncogene product's role in viral cytopathic effects is not fully understood.
Purpose of the Study:
- To investigate the cytolytic effect of MVMp on ts 339/NRK rat cells.
- To determine how temperature-sensitive transformation and oncogene expression affect MVMp-induced cell killing.
- To explore the relationship between host cell physiology and parvovirus cytopathic effects.
Main Methods:
- Culturing ts 339/NRK cells with temperature-sensitive transformation.
- Infecting cells with MVMp at restrictive (39.5°C) and permissive (34.5°C) temperatures.
- Analyzing viral uptake, replication, particle production, and cytopathic effects using electron microscopy.
Main Results:
- A shift to permissive temperature significantly increased MVMp-induced cell killing in ts 339/NRK cells.
- Cells expressing a functional v-src oncogene were sensitive to MVMp at both temperatures.
- Despite resistance to killing at restrictive temperatures, MVMp replicated efficiently, with virions accumulating in vacuoles.
Conclusions:
- Host cell transformation and oncogene expression modulate susceptibility to MVMp cytolysis.
- Reversion to a non-transformed state correlates with non-cytocidal parvovirus production.
- Cellular physiology influences parvovirus susceptibility by affecting both replication and cytopathic mechanisms.