摘要
By using Hoechst 33342, rabbit anti calmodulin antibody ,FITC-1abeled goat anti rabbit IgG and SR101(sulfo rhodamine 101) simultaneously to stain individual normal and transformed cells, t-he micrbspectrophotometric analysis demonstrated that 3 markers' which represented the nucleus, calrnodulin and total protein respectively, could be recognized in individualj cells without interference. The phase of the cell cycle was determined by DNA content (Hoechst 33342). We found that in transformed cells (NIH3T3) tsRSV-LA90,cultured at 33 C and transformed C3H10T1/ 2 cells), the ratio of calmodulin to total protein (based on the phases of cell cycle)was higher than that in normal cells (NIH3T3 tsRSV - LA90 cells, cultured at 39C and C3H10T1/2 cells) in every cell cycle phase. This ratio increased obviously only from G1 to S phase in either normal or transformed cells. The results showed that calmodulin really increased during the transformation, and its increase was specific. In the meantime when cells proceeded from G1 to S, the intracellular calmodulin content also increased specifically.
