DocumentCode
2088224
Title
The HSP70 Release Regulates the Immune Response of Tumor Cells in PDT Treatment
Author
Zhou, Fei-Fan ; Da Xing ; Chen, Wei
Author_Institution
South China Normal Univ., Guangzhou
fYear
2007
fDate
23-27 May 2007
Firstpage
1003
Lastpage
1007
Abstract
Heat shock protein70 (HSP70)is expressed plentifully in tumor cells, and it could regulate tumor immunity. Recent studies show that PDT induce cell surface expression and release HSPs from the treated cells. HSPs have critical role in PDT-induced immune responses, but the immune regulate mechanism of HSP70 and the dynamic of HSP70 interaction with macrophage induced by PDT have not been reported. In present study, YFP-HSP70 was used to monitor the dynamic distribution of HSP70 in real time. With confocal laser scanning microscope (LSM), we detected the dynamic of HSP70 distribution and the interaction with macrophage after PDT treatment. In order to further discuss the immune regulate mechanism of HSP70 after PDT, we also detected TNF-alpha released from macrophages induced by HSP70 with TNF-alpha ELISA. The results showed that PDT treated tumor cells captured by macrophages, and activated the macrophages and induced TNF-alpha release. In addition, the immune effect on overall expression HSP70 cells was higher than normal cells, and decreased evidently when HSP70 was blocked. Our data suggest that HSP70 may serves as a danger signal for immune cells and induce immune responses to regulate the efficacy of PDT.
Keywords
cellular biophysics; molecular biophysics; optical microscopy; photodynamic therapy; proteins; tumours; HSP70; cell surface expression; confocal laser scanning microscope; heat shock protein70; immune regulate mechanism; macrophage; photodynamic therapy; tumor cells; Biomedical engineering; Biomembranes; Electric shock; Immune system; Laser theory; Medical treatment; Neoplasms; Proteins; Surface treatment; Tumors;
fLanguage
English
Publisher
ieee
Conference_Titel
Complex Medical Engineering, 2007. CME 2007. IEEE/ICME International Conference on
Conference_Location
Beijing
Print_ISBN
978-1-4244-1077-4
Electronic_ISBN
978-1-4244-1078-1
Type
conf
DOI
10.1109/ICCME.2007.4381891
Filename
4381891
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