Morita Y, Siraganian R P, Tang C K, Chiang P K
Biochem Pharmacol. 1982 Jun 1;31(11):2111-3. doi: 10.1016/0006-2952(82)90428-2.
3-deaza-SIBA, a postulated analogue of S-adenosylhomocysteine, inhibited the IgE-mediated histamine release and blocked both the choline uptake by the rat basophilic leukemia cells and the incorporation of choline into phosphatidylcholine and lysophosphatidylcholine. Unlike inhibitors of methylation which inhibit only dextran- and IgE-mediated reactions, 3-deaza-SIBA also blocked the histamine release from mast cells induced by other secretagogues, such as compound 48/80, ionophore A23187, polymyxin B and ATP. 3-Deaza-SIBA may perturb membrane functions of basophilic leukemia cells and mast cells by inhibiting the biosynthesis of phosphatidylcholine via choline incorporation, the turnover of which is probably required for cellular degranulation and the release of histamine. Previous studies with 3-deaza-SIBA have been mainly interpreted in terms of its structural similarity to S-adenosylhomocysteine and its potential use as an inhibitor of methylation reactions. In light of our present findings, experiments utilizing 3-deaza-SIBA as a biochemical probe have to be carefully interpreted.
3-脱氮-SIBA是一种推测的S-腺苷同型半胱氨酸类似物,它抑制IgE介导的组胺释放,并阻断大鼠嗜碱性白血病细胞对胆碱的摄取以及胆碱掺入磷脂酰胆碱和溶血磷脂酰胆碱的过程。与仅抑制右旋糖酐和IgE介导反应的甲基化抑制剂不同,3-脱氮-SIBA还能阻断由其他促分泌剂诱导的肥大细胞组胺释放,如化合物48/80、离子载体A23187、多粘菌素B和ATP。3-脱氮-SIBA可能通过抑制胆碱掺入导致的磷脂酰胆碱生物合成来扰乱嗜碱性白血病细胞和肥大细胞的膜功能,而磷脂酰胆碱的周转可能是细胞脱颗粒和组胺释放所必需的。先前关于3-脱氮-SIBA的研究主要是基于其与S-腺苷同型半胱氨酸的结构相似性以及作为甲基化反应抑制剂的潜在用途来解释的。鉴于我们目前的研究结果,利用3-脱氮-SIBA作为生化探针的实验必须谨慎解读。