Katsuda S, Okada Y, Nakanishi I, Tanaka J
Department of Pathology, School of Medicine, Kanazawa University, Japan.
Exp Mol Pathol. 1988 Feb;48(1):48-58. doi: 10.1016/0014-4800(88)90045-7.
Our preliminary study has shown that dimethyl sulfoxide (DMSO) has an inhibitory effect on the proliferation of cultured arterial smooth muscle cells and promotes phenotypic modulation from the synthetic state to the contractile state. In the present study we have examined the effect of DMSO with special attention to relationship between cell growth and cytoplasmic microtubules. DMSO inhibited DNA synthesis and cell division, and concomitantly promoted microtubule assembly. Initiation of DNA synthesis and cell division of nonproliferating cells by platelet-derived growth factor (PDGF) was also inhibited in the presence of 1% DMSO. A 12-hr incubation with 10(-6) M colchicine caused disruption of microtubules; however, pretreatment with 1% DMSO for 24 hr prevented the disruption, indicating that DMSO has a stabilizing action on microtubules. A 24-hr exposure to PDGF resulted in microtubule depolymerization, while the addition of 1% DMSO prevented the depolymerization. These results suggest that DMSO inhibits DNA synthesis of cultured smooth muscle cells by stabilizing cytoplasmic microtubules.
我们的初步研究表明,二甲基亚砜(DMSO)对培养的动脉平滑肌细胞增殖具有抑制作用,并促进其从合成状态向收缩状态的表型调节。在本研究中,我们特别关注了DMSO对细胞生长与细胞质微管之间关系的影响。DMSO抑制DNA合成和细胞分裂,同时促进微管组装。在1% DMSO存在的情况下,血小板衍生生长因子(PDGF)引发的非增殖细胞DNA合成和细胞分裂也受到抑制。用10(-6) M秋水仙碱孵育12小时会导致微管破坏;然而,用1% DMSO预处理24小时可防止这种破坏,这表明DMSO对微管具有稳定作用。暴露于PDGF 24小时会导致微管解聚,而添加1% DMSO可防止解聚。这些结果表明,DMSO通过稳定细胞质微管来抑制培养的平滑肌细胞的DNA合成。