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渥曼青霉素抑制非钙依赖性甘露糖6-磷酸受体掺入反式高尔基体网络来源的网格蛋白包被小泡。

Inhibition of calcium-independent mannose 6-phosphate receptor incorporation into trans-Golgi network-derived clathrin-coated vesicles by wortmannin.

作者信息

Gaffet P, Jones A T, Clague M J

机构信息

Physiological Laboratory, University of Liverpool, Liverpool L69 3BX, United Kingdom.

出版信息

J Biol Chem. 1997 Sep 26;272(39):24170-5. doi: 10.1074/jbc.272.39.24170.

Abstract

The transport of pro-cathepsin D from the trans-Golgi network (TGN) to the endosomal pathway is dependent on binding to the calcium-independent mannose 6-phosphate receptor (ci-M6PR), which is incorporated into TGN-derived clathrin-coated transport vesicles (CCVs). Inhibition of this transport step by wortmannin has led to the proposal that it is dependent upon a phosphoinositide 3-kinase activity necessary for ci-M6PR recruitment into TGN-derived CCVs or in the formation of those vesicles (Brown, W. J., DeWald, D. B., Emr, S. D., Plutner, H., and Balch, W. E. (1995) J. Cell Biol. 130, 781-796; Davidson, H. W. (1995) J. Cell Biol. 130, 797-806). In this study we have addressed the effect of wortmannin on the TGN step of the ci-M6PR cycle. CCVs from K562 cells, pretreated or not with 250 nM wortmannin, were purified on equilibrium density gradients. Quantification of TGN-derived CCVs, assessed by gamma-adaptin content in purified vesicle fractions, showed that the formation of the vesicles was only marginally decreased after 20 min of treatment with the drug, while for the same wortmannin treatment, the amount of ci-M6PR recruited into those vesicles was decreased by 70% compared with control. At a later time point (2 h), a reduction in the amount of gamma-adaptin in CCV fractions was also observed. These findings demonstrate that inhibition of ci-M6PR recruitment into CCVs but not of vesicle formation is the primary reason for the observed defect in cathepsin D transport following wortmannin treatment.

摘要

组织蛋白酶D前体从反式高尔基体网络(TGN)转运至内体途径,依赖于与不依赖钙的甘露糖6-磷酸受体(ci-M6PR)的结合,该受体被整合到源自TGN的网格蛋白包被转运囊泡(CCV)中。渥曼青霉素对这一转运步骤的抑制作用,使人提出该转运步骤依赖于一种磷酸肌醇3-激酶活性,这一活性对于ci-M6PR募集到源自TGN的CCV中或这些囊泡的形成是必需的(Brown, W. J., DeWald, D. B., Emr, S. D., Plutner, H., and Balch, W. E. (1995) J. Cell Biol. 130, 781 - 796; Davidson, H. W. (1995) J. Cell Biol. 130, 797 - 806)。在本研究中,我们探讨了渥曼青霉素对ci-M6PR循环中TGN步骤的影响。用250 nM渥曼青霉素预处理或未预处理的K562细胞的CCV,在平衡密度梯度上进行纯化。通过纯化囊泡组分中的γ-衔接蛋白含量评估源自TGN的CCV的定量分析表明,用该药物处理20分钟后,囊泡的形成仅略有减少,而对于相同的渥曼青霉素处理,与对照相比,募集到这些囊泡中的ci-M6PR量减少了70%。在稍后的时间点(2小时),还观察到CCV组分中γ-衔接蛋白量的减少。这些发现表明,渥曼青霉素处理后观察到的组织蛋白酶D转运缺陷的主要原因是抑制了ci-M6PR募集到CCV中,而不是囊泡形成。

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