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Published on: December 31, 2014
Sensitivity of transformed fibroblasts for intercellular induction of apoptosis is determined by their transformed
1Abteilung Virologie, Institut für Medizinische Mikrobiologie und Hygiene Universität Freiburg, Germany.
Abstract:
Intercellular induction of apoptosis defines a potential control mechanism of oncogenesis. It is based on induction of apoptosis in transformed fibroblasts by neighboring nontransformed fibroblasts. Transforming growth factor type beta (TGF-beta) represents the initial triggering molecule to induce nontransformed cells to release apoptosis-inducing factors. To test whether sensitivity for intercellular induction of apoptosis is directly dependent on the transformed phenotype, v-src-transformed rat fibroblasts and emerging revertants were tested for their sensitivity. All transformed cell clones were sensitive, whereas all revertant clones had lost their sensitivity in parallel with the loss of the transformed phenotype. In addition, revertants had regained the potential to induce apoptosis in transformed cells. Sensitivity to intercellular induction of apoptosis is therefore directly dependent on the transformed phenotype, whereas the ability to induce apoptosis is a specific feature of nontransformed fibroblasts.
Insights
Nontransformed cells induce apoptosis in cancer cells, a process regulated by transforming growth factor beta (TGF-beta). This sensitivity to apoptosis induction is linked to the transformed cell phenotype, with normal cells initiating this process.
Area of Science:
- Cell biology
- Cancer research
- Molecular oncology
Background:
- Intercellular apoptosis induction is a potential mechanism for controlling oncogenesis.
- Transforming growth factor beta (TGF-beta) initiates apoptosis induction in neighboring cells.
- The relationship between the transformed phenotype and apoptosis sensitivity requires further investigation.
Purpose of the Study:
- To determine if sensitivity to intercellular apoptosis induction is dependent on the transformed cell phenotype.
- To investigate the role of v-src-transformed rat fibroblasts and their revertants in this process.
- To clarify the distinct roles of transformed and non-transformed cells in apoptosis signaling.
Main Methods:
- Utilizing v-src-transformed rat fibroblasts and their revertant clones.
- Assessing the sensitivity of these cell lines to intercellular apoptosis induction.
- Evaluating the capacity of revertant cells to induce apoptosis in transformed cells.
Main Results:
- All transformed fibroblast clones exhibited sensitivity to intercellular apoptosis induction.
- Revertant clones, having lost the transformed phenotype, lost sensitivity to apoptosis induction.
- Revertant cells regained the ability to induce apoptosis in transformed cells.
- Sensitivity to apoptosis induction correlates directly with the transformed phenotype.
Conclusions:
- Sensitivity to intercellular apoptosis induction is directly dependent on the transformed cell phenotype.
- The ability to induce apoptosis is a characteristic feature of non-transformed fibroblasts.
- This study elucidates a novel cell-cell communication pathway in cancer regulation.
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