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Bacillus intermedius ribonuclease as inhibitor of cell proliferation and membrane current
O Ilinskaya1, K Decker, A Koschinski
1Department of Microbiology, Kazan State University, Kremlevskaya Street 18, 420008 Kazan, Russia.
Abstract:
The antiproliferative action of the guanine-specific ribonuclease secreted by Bacillus intermedius (binase) was studied in different chicken and mouse cell lines. The proliferation rate of chicken embryo fibroblasts, either normal or Rous sarcoma virus-transformed, was significantly reduced by binase treatment. Among mouse fibroblasts, v-ras-transformed NIH3T3 cells were sensitive to binase, whereas the growth of non-transformed, v-src-transformed or v-fms-transformed NIH3T3 cells was not affected. A 48 h treatment with binase inhibited the Ca2+-dependent K+ current of v-ras-transformed NIH3T3 cells but had no effect on this membrane current in non-transformed and in v-src- or v-fms-transformed NIH3T3 cells. Our results suggest that mammalian cells expressing the ras-oncogene are a potential target for the antiproliferative action of binase.
Insights
Bacillus intermedius ribonuclease (binase) effectively reduces proliferation in ras-oncogene-expressing mammalian cells. This enzyme also inhibits calcium-dependent potassium currents in these specific cells, indicating a targeted antiproliferative effect.
Area of Science:
- Biochemistry
- Cell Biology
- Molecular Oncology
Background:
- Bacillus intermedius ribonuclease (binase) is a guanine-specific enzyme with known biological activities.
- Oncogenes, such as ras, play a critical role in cellular transformation and proliferation.
Purpose of the Study:
- To investigate the antiproliferative effects of binase on various chicken and mouse cell lines.
- To determine if binase specifically targets cells expressing the ras oncogene.
- To examine the impact of binase on cellular membrane currents in relation to oncogene expression.
Main Methods:
- Treatment of normal and oncogene-transformed chicken and mouse cell lines with binase.
- Assessment of cell proliferation rates following binase exposure.
- Electrophysiological recordings to measure Ca2+-dependent K+ currents in treated cells.
Main Results:
- Binase significantly reduced the proliferation of chicken embryo fibroblasts and v-ras-transformed NIH3T3 mouse cells.
- Non-transformed, v-src-transformed, and v-fms-transformed NIH3T3 cells showed no significant growth inhibition by binase.
- Binase treatment inhibited the Ca2+-dependent K+ current in v-ras-transformed NIH3T3 cells but not in other cell types.
Conclusions:
- Mammalian cells expressing the ras oncogene are sensitive to the antiproliferative effects of binase.
- Binase exhibits selective toxicity towards ras-transformed cells.
- The observed inhibition of ion currents suggests a mechanism for binase's antiproliferative action in ras-expressing cells.
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