Tüscher O, Lorra C, Bouma B, Wirtz K W, Huttner W B
Department of Neurobiology, University of Heidelberg, Germany.
FEBS Lett. 1997 Dec 15;419(2-3):271-5. doi: 10.1016/s0014-5793(97)01471-3.
Phosphatidylinositol transfer protein (PITP) and phospholipase D (PLD) stimulate the formation of constitutive secretory vesicles (CSVs) and immature secretory granules (ISGs) from the trans-Golgi network (TGN) in a cell-free system. The stimulatory effects of PITP and PLD are additive. Stimulation by either PITP or PLD is blocked by geneticin, a member of the aminoglycoside antibiotics known to bind to phosphoinositides. Since the PLD we used is insensitive to geneticin, our results suggest that phosphoinositides promote secretory vesicle formation as downstream effectors of both PITP and PLD, possibly via the recruitment of proteins mediating membrane budding and fission.
磷脂酰肌醇转移蛋白(PITP)和磷脂酶D(PLD)在无细胞体系中可刺激反式高尔基体网络(TGN)形成组成型分泌囊泡(CSV)和未成熟分泌颗粒(ISG)。PITP和PLD的刺激作用具有加和性。PITP或PLD的刺激作用均被遗传霉素阻断,遗传霉素是一种已知可与磷酸肌醇结合的氨基糖苷类抗生素。由于我们使用的PLD对遗传霉素不敏感,我们的结果表明,磷酸肌醇作为PITP和PLD的下游效应物促进分泌囊泡形成,可能是通过招募介导膜出芽和裂变的蛋白质来实现的。