Inhibition of multinucleation of cells treated with cytochalasin-B by cyclic dibutyryl-AMP
- PMID: 176079
Inhibition of multinucleation of cells treated with cytochalasin-B by cyclic dibutyryl-AMP
Abstract
Multinucleation of SV40-transformed mouse cells was induced by Cytochalasin-B as a result of inhibition of cytokinesis. Multinucleated cells with nuclei, whose number is other than that that can be obtained by raising the power of 2, were frequently observed. By simultaneous addition of Cytochalasin-B and cylic dibutyryl-AMP to SV40-transformad mouse cellls, multinucleation was fairly inhibited and the predominance of the cells with 2 or 4 nuclei was characteristic. In case of normal mouse cells (BALB/3T3), addition of both Cytochalasin-B and cyclic dibutyryl-AMP lessened the number of nucleic in a cell compared with treatment of the cells with Cytochalasin-B alone. These results suggested that cyclic dibutyryl-AMP inhibited multinucleation of cells treated with Cytochalasin-B and that the chemical regulated the division of nuclei in a cell to divide simultaneously.
Similar articles
-
DNA synthesis and multinucleation of mouse cells infected with SV40 in the presence of cytochalasin B.J Gen Virol. 1980 Jan;46(1):237-42. doi: 10.1099/0022-1317-46-1-237. J Gen Virol. 1980. PMID: 6243345
-
Cytochalasin B-induced multinucleation of murine sarcoma virus-transformed cells. Inhibition by sodium butyrate.Exp Cell Res. 1979 Jan;118(1):31-7. doi: 10.1016/0014-4827(79)90580-9. Exp Cell Res. 1979. PMID: 215423 No abstract available.
-
[Role of multipolar mitoses in the proliferation of multinucleate cells induced by cytochalasin B].Tsitologiia. 1987 Jul;29(7):794-801. Tsitologiia. 1987. PMID: 3672640 Russian.
-
Control of nuclear division and chromosomal abnormalities in cytochalasin B-treated normal and transformed cells.Front Biol. 1978;46:217-55. Front Biol. 1978. PMID: 352742 Review. No abstract available.
-
Enucleation of cultured animal cells by cytochalasin B.Front Biol. 1978;46:161-89. Front Biol. 1978. PMID: 352740 Review. No abstract available.