Departments of Functional Genomics, Clinical Genetics, VUmc, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV, Amsterdam, The Netherlands.
Clinical Genetics, VUmc, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam and VU Medical Center, de Boelelaan 1087, 1081 HV, Amsterdam, The Netherlands.
Nat Commun. 2018 Aug 24;9(1):3421. doi: 10.1038/s41467-018-05699-z.
The SNAREs Vti1a/1b are implicated in regulated secretion, but their role relative to canonical exocytic SNAREs remains elusive. Here, we show that synaptic vesicle and dense-core vesicle (DCV) secretion is indeed severely impaired in Vti1a/b-deficient neurons. The synaptic levels of proteins that mediate secretion were reduced, down to 50% for the exocytic SNARE SNAP25. The delivery of SNAP25 and DCV-cargo into axons was decreased and these molecules accumulated in the Golgi. These defects were rescued by either Vti1a or Vti1b expression. Distended Golgi cisternae and clear vacuoles were observed in Vti1a/b-deficient neurons. The normal non-homogeneous distribution of DCV-cargo inside the Golgi was lost. Cargo trafficking out of, but not into the Golgi, was impaired. Finally, retrograde Cholera Toxin trafficking, but not Sortilin/Sorcs1 distribution, was compromised. We conclude that Vti1a/b support regulated secretion by sorting secretory cargo and synaptic secretion machinery components at the Golgi.
SNAREs Vti1a/1b 参与调节分泌,但它们相对于经典的胞吐 SNAREs 的作用仍不清楚。在这里,我们表明 Vti1a/b 缺陷神经元中的突触囊泡和致密核心囊泡 (DCV) 分泌确实严重受损。介导分泌的蛋白质的突触水平降低,外向 SNARE SNAP25 降低至 50%。SNAP25 和 DCV 货物向轴突的传递减少,这些分子在高尔基体内积累。Vti1a 或 Vti1b 的表达可以挽救这些缺陷。在 Vti1a/b 缺陷神经元中观察到扩展的高尔基池和清晰的空泡。高尔基体内 DCV 货物的正常非均匀分布丢失。货物从高尔基体内运出,但不是进入高尔基体内的运输受损。最后,逆行霍乱毒素运输受损,但 Sorcs1 分布不受影响。我们得出结论,Vti1a/b 通过在高尔基体内分拣分泌货物和突触分泌机制成分来支持调节分泌。