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Cellular transformation and the 'morphologic phenotype' of transformed cells
Nature
|August 17, 1978
Summary
The expression of the Rous sarcoma virus (RSV) transforming gene (src) alters fibroblast cell properties, primarily by reducing cell-to-substratum adhesion. These changes in the morphologic phenotype resemble effects seen with peptide hormones like insulin.
Area of Science:
- Molecular Biology
- Cell Biology
- Virology
Background:
- The transforming gene (src) product from RNA tumor viruses influences cell growth and characteristics.
- Transformed cells exhibit altered adhesion, appearance, and surface properties, collectively termed the 'morphologic phenotype'.
- Diminished cell-to-substratum adhesion is a key factor in the morphologic phenotype of src-expressing cells.
Purpose of the Study:
- To investigate the impact of src gene expression on cultured fibroblasts.
- To explore the underlying mechanisms contributing to the morphologic phenotype of transformed cells.
- To compare the effects of src expression with those of peptide hormones.
Main Methods:
- Analysis of gene expression in cultured fibroblasts.
- Observation and characterization of cellular morphology and adhesion properties.
- Investigation of the roles of cyclic AMP and cell surface proteins (CSP).
Main Results:
- Src expression promotes fibroblast growth.
- Src expression significantly alters cell adhesion, appearance, and surface properties.
- The observed changes in the morphologic phenotype are largely attributed to reduced cell-to-substratum adhesion.
Conclusions:
- Src gene product expression profoundly affects fibroblast characteristics.
- The morphologic phenotype induced by src is primarily mediated by decreased cell adhesion.
- The cellular responses to src expression share similarities with peptide hormone actions, such as insulin.