The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities

被引:91
作者
Campanella, Claudia [1 ,2 ]
Bucchieri, Fabio [1 ,2 ]
Merendino, Anna M. [1 ]
Fucarino, Alberto [1 ]
Burgio, Giosalba [3 ,4 ]
Corona, Davide F. V. [3 ,4 ]
Barbieri, Giovanna [5 ]
David, Sabrina [1 ]
Farina, Felicia [1 ]
Zummo, Giovanni [1 ]
de Macario, Everly Conway [6 ,7 ]
Macario, Alberto J. L. [2 ,6 ,7 ]
Cappello, Francesco [1 ,2 ]
机构
[1] Univ Palermo, Dipartimento BIONEC, Sez Anat Umana, Palermo, Italy
[2] Ist Euro Mediterraneo Sci & Tecnol, Palermo, Italy
[3] Univ Palermo, Dipartimento STEMBIO, Palermo, Italy
[4] Dulbecco Telethon Inst, Palermo, Italy
[5] CNR, Ist Biomed & Immunol Mol, Palermo, Italy
[6] Univ Maryland, Sch Med, Dept Microbiol & Immunol, Baltimore, MD 21201 USA
[7] IMET, Baltimore, MD USA
关键词
HEAT-SHOCK PROTEINS; MITOCHONDRIAL CHAPERONES; MAMMALIAN-CELLS; STRESS-PROTEINS; CELLULAR STRESS; CANCER; HEAT-SHOCK-PROTEIN-60; IDENTIFICATION; ACTIVATION; LOCALIZATION;
D O I
10.1371/journal.pone.0042008
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: In a previous work we showed for the first time that human tumor cells secrete Hsp60 via exosomes, which are considered immunologically active microvesicles involved in tumor progression. This finding raised questions concerning the route followed by Hsp60 to reach the exosomes, its location in them, and whether Hsp60 can be secreted also via other mechanisms, e. g., by the Golgi. We addressed these issues in the work presented here. Principal Findings: We found that Hsp60 localizes in the tumor cell plasma membrane, is associated with lipid rafts, and ends up in the exosomal membrane. We also found evidence that Hsp60 localizes in the Golgi apparatus and its secretion is prevented by an inhibitor of this organelle. Conclusions/Significance: We propose a multistage process for the translocation of Hsp60 from the inside to the outside of the cell that includes a combination of protein traffic pathways and, ultimately, presence of the chaperonin in the circulating blood. The new information presented should help in designing future strategies for research and for developing diagnostic-monitoring means useful in clinical oncology.
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页数:8
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