Growth retardation in glioma cells cocultured with cells overexpressing a gap junction protein.
- 1 November 1992
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 89 (21) , 10218-10221
- https://doi.org/10.1073/pnas.89.21.10218
Abstract
To examine the role of gap-junctional intercellular communication in controlling cell proliferation, we have transfected C6 glioma cells with connexin 43 cDNA. The growth of transfected clones was dramatically reduced compared with nontransfected glioma cells. To further characterize the role of gap junctions in controlling proliferation, we have examined the growth of C6 cells cocultured with transfected cells overexpressing connexin 43. Although C6 cells grew at their normal rate when cocultured with nontransfected C6 cells, when cocultured with connexin 43-overexpressing cells they displayed a dramatic reduction in growth rate. Furthermore, a significant, dose-dependent reduction in cell proliferation was noted when C6 cells were cultured in medium conditioned by transfected cells. This effect correlated with the level of connexin 43 expression. These results suggest that the decreased cell proliferation rate of transfected cells and C6 cells cultured with them is due to the secretion of a growth inhibitory factor(s) and that the secretion of this factor may be linked to the level of gap junctional intercellular communication.Keywords
This publication has 26 references indexed in Scilit:
- Intercellular calcium signaling via gap junctions in glioma cells.The Journal of cell biology, 1992
- Response of low-passage human malignant gliomas in vitro to stimulation and selective inhibition of growth factor-mediated pathwaysJournal of Neurosurgery, 1991
- Differential regulation of communication by retinoic acid in homologous and heterologous junctions between normal and transformed cells.The Journal of cell biology, 1991
- Interaction with normal cells suppresses the transformed phenotype of v-myc-transformed quail muscle cellsCell, 1989
- Specific viral oncogenes cause differential effects on cell‐to‐cell communication, relevant to the suppression of the transformed phenotype by normal cellsMolecular Carcinogenesis, 1988
- Growth control in cultured 3T3 fibroblasts. V. Purification of an Mr 13,000 polypeptide responsible for growth inhibitory activity.The Journal of cell biology, 1986
- Growth inhibition of transformed cells correlates with their junctional communication with normal cellsPublished by Elsevier ,1986
- Properties of a cell growth inhibitor produced by mouse embryo fibroblastsJournal of Cellular Physiology, 1983
- Growth control in cultured 3T3 fibroblasts II. Molecular properties of a fraction enriched in growth inhibitory activity.The Journal of cell biology, 1982
- Junctional intercellular communication and the control of growthBiochimica et Biophysica Acta (BBA) - Reviews on Cancer, 1979