Cholesterol regulates prostasome release from secretory lysosomes in PC-3 human prostate cancer cells

被引:60
作者
Llorente, Alicia [1 ]
van Deurs, Bo
Sandvig, Kirsten
机构
[1] Univ Oslo, Norwegian Radium Hosp, Fac Div, Rikshosp Radiumhosp Med Ctr,Ctr Canc Biomed, N-0310 Oslo, Norway
[2] Univ Copenhagen, Dept Cellular & Mol Med, DK-2200 Copenhagen N, Denmark
[3] Univ Oslo, Dept Mol Biosci, N-0316 Oslo, Norway
关键词
prostasomes; PC-3; cells; secretion; cholesterol; secretory lysosomes; prostate cancer;
D O I
10.1016/j.ejcb.2007.05.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prostasomes are vesicles secreted by epithelial cells of the prostate gland. However, little is known about the mechanism and the regulation of prostasome secretion. Since endocytic organelles may be involved in prostasome release, PC-3-derived prostasomes were investigated by Western blot analysis for the presence of marker proteins normally associated with these organelles. Prostasomes secreted by PC-3 cells contain clathrin, Tsg101, Hrs, Rab11, Rab5, LAMP-1, LAMP-2, LAMP-3/CD63, and annexin II. Moreover, electron microscopy of PC-3 cells revealed the presence of characteristic multivesicular body-like secretory lysosomes containing vesicles with the same size-distribution as released prostasomes. Ultrastructural immunogold labelling showed that LAMP-1, LAMP-2 and LAMP-3/CD63 were associated with these vesicles. In addition, we have investigated whether cholesterol plays a role in prostasome release by the human prostate cancer cell line PC-3. Interestingly, prostasome release was significantly increased when the cholesterol levels of PC-3 cells were reduced by the cholesterol-sequestering agent methyl-beta-cyclodextrin (MBCD), or by treatment with lovastatin and mevalonate. In conclusion, these studies indicate that cholesterol plays an important role in the release of prostasomes by the human prostate cancer PC-3 cells, and suggest that prostasomes may be released after fusion of secretory lysosomes with the plasma membrane. (c) 2007 Elsevier GmbH. All rights reserved.
引用
收藏
页码:405 / 415
页数:11
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