Tadvalkar G, Pinto da Silva P
J Cell Biol. 1983 May;96(5):1279-87. doi: 10.1083/jcb.96.5.1279.
We report here rapid assembly of gap junctions in prostate epithelial cells in vitro. Assembly of gap junctions can be induced by incubation at 0 degrees C followed by incubation at 37 degrees C. Colchicine (10(-5) M, 10(-3) M) and cytochalasin B (25 micrograms/ml), 100 micrograms/ml) at room temperature or at 37 degrees C also induce assembly of gap junctions. Assembly of the junctions proceeds even in the presence of a metabolic inhibitor (dinitrophenol) or of an inhibitor of protein synthesis (cycloheximide). We conclude that assembly of gap junctions can proceed from a pool of pre-existing precursors. The experimental conditions that result in gap-junction assembly involve perturbation of the cytoskeleton. Therefore, we propose that the assembly of gap junctions requires convergent migration of precursor molecules whose positional control in the membrane is released by perturbation of the cytoskeleton. Aggregates of particles and rugosities, whose distribution size and shape is similar to that of gap junctions, may represent intermediate assembly stages. This would indicate that the final stages in the assembly take place only after convergence of the precursor molecules to the junctional site and involve profound conformational changes required for establishment of fully assembled connexons.
我们在此报告前列腺上皮细胞中缝隙连接在体外的快速组装。在0℃孵育随后在37℃孵育可诱导缝隙连接的组装。秋水仙碱(10⁻⁵M、10⁻³M)和细胞松弛素B(25微克/毫升、100微克/毫升)在室温或37℃下也可诱导缝隙连接的组装。即使存在代谢抑制剂(二硝基苯酚)或蛋白质合成抑制剂(放线菌酮),连接的组装仍可进行。我们得出结论,缝隙连接的组装可从预先存在的前体池中进行。导致缝隙连接组装的实验条件涉及细胞骨架的扰动。因此,我们提出缝隙连接的组装需要前体分子的趋同迁移,其在膜中的位置控制通过细胞骨架的扰动而释放。颗粒聚集体和皱纹,其分布大小和形状与缝隙连接相似,可能代表组装的中间阶段。这表明组装的最终阶段仅在将前体分子聚集到连接位点之后发生,并且涉及建立完全组装的连接子所需的深刻构象变化。