Funato K, Beron W, Yang C Z, Mukhopadhyay A, Stahl P D
Animal and Cellular Systems Lab, The Institute of Physical and Chemical Research (RIKEN), Hirosawa 2-1, Wako-shi, Saitama 351-01, Japan.
J Biol Chem. 1997 Jun 27;272(26):16147-51. doi: 10.1074/jbc.272.26.16147.
We have reconstituted fusion between phagosomes and lysosomes in streptolysin O-permeabilized J774-E macrophages. Fusion was assessed by measuring the delivery of avidin-conjugated horseradish peroxidase pre-internalized into lysosomes to phagosomes containing biotinylated beta-glucuronidase-conjugated paramagnetic beads (1-2 microm). Fusion was dependent on energy and exogenously supplied cytosol. Phagosome-lysosome fusion was greatly inhibited when microtubules were depolymerized by nocodazole treatment, suggesting that fusion occurs via microtubule-dependent transport. Furthermore, fusion was inhibited by GTPgammaS and Rab GDP dissociation inhibitor. These results suggest that rab proteins are involved in the regulation of fusion. Lastly, anti-NEM-sensitive factor (NSF) antibodies inhibited fusion, and addition of recombinant NSF wild type partially restored the fusogenic activity, indicating that NSF is required for fusion between phagosomes and lysosomes.
我们已在经链球菌溶血素O通透处理的J774-E巨噬细胞中重建了吞噬体与溶酶体之间的融合。通过测量预先内化到溶酶体中的抗生物素蛋白结合辣根过氧化物酶向含有生物素化β-葡萄糖醛酸酶结合的顺磁珠(1-2微米)的吞噬体的传递来评估融合。融合依赖于能量和外源提供 cytosol。当用诺考达唑处理使微管解聚时,吞噬体-溶酶体融合受到极大抑制,这表明融合是通过微管依赖性转运发生的。此外,GTPγS和Rab GDP解离抑制剂抑制融合。这些结果表明rab蛋白参与融合的调节。最后,抗NEM敏感因子(NSF)抗体抑制融合,添加重组NSF野生型部分恢复了融合活性,表明NSF是吞噬体与溶酶体之间融合所必需的。