Billah M M, Siegel M I
Biochem Biophys Res Commun. 1984 Jan 30;118(2):629-35. doi: 10.1016/0006-291x(84)91349-4.
Human polymorphonuclear leukocytes in the presence of the Ca2+ ionophore A23187 plus Ca2+ incorporated exogenously-added [3H]acetate or 1-0-[3H]-alkyl-sn-glycero-3-phosphocholine (lysoplatelet-activating factor) into platelet-activating factor (PAF,1-0-alkyl-2-acetyl-sn-glycero-3-phosphocholine). The incorporation of these radiolabels into PAF by stimulated neutrophils was inhibited by the calmodulin antagonists, trifluoperazine and N-(6-aminohexyl)-5-chloro-1-naphthalene sulfonamide. These two drugs were active at concentrations similar to their respective binding constants to purified calmodulin, suggesting a possible involvement of calcium-activated calmodulin in PAF biosynthesis.
在存在Ca2+离子载体A23187和外源性添加的Ca2+的情况下,人多形核白细胞将添加的[3H]乙酸盐或1-O-[3H]-烷基-sn-甘油-3-磷酸胆碱(溶血血小板活化因子)掺入血小板活化因子(PAF,1-O-烷基-2-乙酰基-sn-甘油-3-磷酸胆碱)中。钙调蛋白拮抗剂三氟拉嗪和N-(6-氨基己基)-5-氯-1-萘磺酰胺抑制了受刺激的中性粒细胞将这些放射性标记物掺入PAF的过程。这两种药物在与其各自与纯化钙调蛋白的结合常数相似的浓度下具有活性,表明钙激活的钙调蛋白可能参与PAF的生物合成。