Klingenstein R J, Dickler H B
Scand J Immunol. 1979;10(2):145-52. doi: 10.1111/j.1365-3083.1979.tb03269.x.
The effects of pharmacologic agents on the immune-complex-induced redistribution of B-lymphocyte Fc receptors (and, as a control, the anti-Ig induced redistribution of surface Ig) were examined. Immune-complex-induced capping of B-cell Fc receptors was moderately to markedly inhibited by the combination of colchicine and cytochalasin B, the Ca++ ionophore A23187, and the local anaesthetic lidocaine but was only slightly inhibited by cytochalasin B alone and was not inhibited by colchicine alone. Inhibition of capping was not due to the inhibition of binding of immune complexes to the B-lymphocytes or to decreased cell viability since these effects were absent. Preformed immune complex-Fc receptor caps were disrupted by A23187, lidocaine, and the combination of colchicine and cytochalasin B, but not by either colchicine or cytochalasin B alone. The effects of the pharmacologic agents were similar for Fc receptors and surface Ig in all cases. These results suggest that ligand bound Fc receptors are affected by cytoskeletal structures and that the ligand-induced redistribution of two distinct B lymphocyte surface receptors (fc receptors and surface Ig) occurs by similar or identical mechanisms.
研究了药理制剂对免疫复合物诱导的B淋巴细胞Fc受体再分布(以及作为对照的抗Ig诱导的表面Ig再分布)的影响。秋水仙碱和细胞松弛素B、Ca++离子载体A23187以及局部麻醉剂利多卡因的组合可中度至显著抑制免疫复合物诱导的B细胞Fc受体帽化,但单独使用细胞松弛素B仅产生轻微抑制,单独使用秋水仙碱则无抑制作用。帽化的抑制并非由于免疫复合物与B淋巴细胞结合的抑制或细胞活力降低,因为不存在这些效应。预先形成的免疫复合物-Fc受体帽可被A23187、利多卡因以及秋水仙碱和细胞松弛素B的组合破坏,但单独使用秋水仙碱或细胞松弛素B则无此作用。在所有情况下,药理制剂对Fc受体和表面Ig的作用相似。这些结果表明,配体结合的Fc受体受细胞骨架结构影响,并且两种不同的B淋巴细胞表面受体(Fc受体和表面Ig)的配体诱导再分布通过相似或相同的机制发生。