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Vacuolin-1 is a cell-permeable inhibitor of Ca2+ dependent fusion of lysosomes to the cell membrane. Vacuolin-1 blocks the Ca2+-dependent exocytosis of lysosomes and prevents the release of lysosomal content without affecting the process of resealing. vacuolin‐1 is a potent and selective PIKfyve inhibitor and inhibits late‐stage autophagy by impairing lysosomal maturation.
Vacuolin-1 (1 μM; Pretreatment 1 hour) blocks ionomycin-induced exocytosis of lysosomes but not of enlargeosomes. It results in vacuolation of lysosomes (A) and complete inhibition of the surface expression of Lamp-1. Vacuolin-1 (1 μM; 20-180 min) disrupts the segregation of inner and limiting membranes characteristic of endosomes and lysosomes. Ultrastructural analysis also shows that vacuolin-1 favours fusion of inner and limiting membranes. Vacuolin-1 (5 or 10 μM; 2 hours) blocks the Ca2+-dependent release of β-hexosaminidase from lysosomes. In HeLa cells, ionomycin results in the expected release of 18-20% of lysosomal β-hexosaminidase. But when cells pretreated with vacuolin-1, releases no more β-hexosaminidase compared with cells that are not exposed to ionomycin (4%).
| Cell Experiment | |
|---|---|
| Cell lines | RBL 2H3 cells and BMMCs |
| Preparation method | RBL-2H3 cells or BMMCs were treated with various concentrations of inhibitors for 30 min before adding vacuolin-1 (final concentration 10 µM). After further 3 h incubation with the inhibitor and vacuolin-1, cell viability was assessed by trypan blue staining. |
| Concentrations | 10 µM |
| Incubation time | 3 h |
| Animal Experiment | |
|---|---|
| Animal models | BALB/c mice |
| Formulation | DMSO and saline |
| Dosages | 15, 20, 30 mg/kg |
| Administration | Oral and I.P. |
| Molecular Weight | 577.42 |
| Formula | C26H24IN7O |
| CAS Number | 351986-85-1 |
| Form | Solid |
| Solubility (25°C) | DMSO 6 mg/mL |
| Storage | -20°C, sealed |
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