Hidaka H, Sasaki Y, Tanaka T, Endo T, Ohno S, Fujii Y, Nagata T
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4354-7. doi: 10.1073/pnas.78.7.4354.
N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7) and its derivatives are putative calmodulin antagonists that bind to calmodulin and inhibit Ca2+/calmodulin-regulated enzyme activities. Autoradiographic studies using tritiated W-7 showed that this compound penetrates the cell membrane, is distributed mainly in the cytoplasm, and inhibits proliferation of Chinese hamster ovary K1 (CHO-K1) cells. Cytoplasmic [3H]W-7 was excluded completely within 6 hr after removal of [3H]W-7 from the culture medium. N-(6-aminohexyl)-1-naphthalenesulfonamide, an analogue of W-7 that interacts only weakly with calmodulin, proved to be a much weaker inhibitor of cell proliferation. CHO-K1 cells were synchronized by shaking during mitosis and then released into the cell cycle in the presence of 25 microM W-7 or 2.5 mM thymidine for 12 hr. Cell division was observed approximately 6 hr later. The results suggest that the effect of W-7 on cell proliferation might be through selective inhibition of the G1/S boundary phase, which is similar to the effect of excess thymidine. This pharmacological demonstration that cytoplasmic calmodulin is involved in cell proliferation is significant; W-7 and its derivatives may be useful tools for research on calmodulin and cell biology-related studies.
N-(6-氨基己基)-5-氯-1-萘磺酰胺(W-7)及其衍生物是公认的钙调蛋白拮抗剂,它们与钙调蛋白结合并抑制Ca2+/钙调蛋白调节的酶活性。使用氚标记的W-7进行的放射自显影研究表明,该化合物可穿透细胞膜,主要分布在细胞质中,并抑制中国仓鼠卵巢K1(CHO-K1)细胞的增殖。从培养基中去除[3H]W-7后6小时内,细胞质中的[3H]W-7被完全清除。N-(6-氨基己基)-1-萘磺酰胺是W-7的类似物,与钙调蛋白的相互作用较弱,事实证明它对细胞增殖的抑制作用要弱得多。在有丝分裂期间通过振荡使CHO-K1细胞同步化,然后在存在25μM W-7或2.5 mM胸苷的情况下释放到细胞周期中12小时。大约6小时后观察到细胞分裂。结果表明,W-7对细胞增殖的影响可能是通过选择性抑制G1/S边界期,这与过量胸苷的作用相似。这种关于细胞质钙调蛋白参与细胞增殖的药理学证明具有重要意义;W-7及其衍生物可能是研究钙调蛋白和细胞生物学相关研究的有用工具。