Abstract
Connexins, the structural components of gap junctions, control cell growth and differentiation and are believed to belong to a family of tumour suppressor genes. Studies on connexin localization in brain showed that several of these proteins were expressed in distinct compartments of the brain in a cell-type specific manner, indicating that different gap junctions play specific roles in the physiology of the mammalian brain. In this report, we first cloned rat connexin-30 cDNA from brain and showed that it was expressed in long-term primary culture of rat astrocytes. In order to examine the potential role of connexin-30 in tumour cell proliferation, we transfected the connexin-30 cDNA into two rat glioma cell lines (9L and C6) which have lost its expression. Transfected clones adequately expressed membrane-bound connexin-30 protein. Connexin-30-expressing clones showed slower growth, lower DNA synthesis and reduced proliferation in soft agar as compared with the parental and control cells. We concluded that connexin-30 may also probably be considered as a tumour suppressor in rat gliomas.
| Original language | English |
|---|---|
| Pages (from-to) | 507-13 |
| Number of pages | 7 |
| Journal | Carcinogenesis |
| Volume | 22 |
| Issue number | 3 |
| Publication status | Published - Mar 2001 |
Keywords
- Amino Acid Sequence
- Animals
- Cloning, Molecular
- Connexin 30
- Connexins/chemistry
- DNA, Complementary
- Gap Junctions/physiology
- Humans
- Molecular Sequence Data
- Polymerase Chain Reaction
- Rats
- Sequence Homology, Amino Acid
- Transfection
- Tumor Cells, Cultured
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