Quantum dot imaging for HSP70 and HSF-1 kinetics in SCC-25 cells with or without leucine deprivation following heat shock

被引:7
作者
Chen, Jun [1 ]
Pan, Jie [1 ]
Zhao, Jianjiang [1 ]
Qiu, Xiaoling [1 ]
Zheng, Junfa [1 ]
Wang, Zhiping [1 ]
Huang, Yuhua [1 ]
Chu, Hongxing [1 ]
机构
[1] Southern Med Univ, Guangdong Prov Stomatol Hosp, Dept Oral Surg, Guangzhou 510280, Guangdong, Peoples R China
关键词
quantum dot; protein kinetics; heat stress; heat shock protein 70; heat shock factor 1; oral squamous cell carcinoma; leucine deprivation; IN-SITU HYBRIDIZATION; CANCER; PROTEIN; NANOCRYSTALS; EXPRESSION; IMMUNOFLUORESCENT; PROTEOMICS; GENOMICS; TARGETS; STRESS;
D O I
10.3892/or.2013.2372
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to develop a quantum dot-based approach for heat shock protein 70 (HSP70) and heat shock factor 1 (HSF-1) kinetics following heat shock, and to discover approaches to thermotherapy based on disrupting the effect of activation of HSF-1 and the accumulation of HSP70 by leucine deprivation. SCC-25 cells cultured with limiting leucine or normal leucine were stressed at 42 degrees C for 30 min, and were cultured for 2,4, 6, 8 and 10 h, respectively. The expression of HSP70 and HSF-1 was observed using confocal laser microscopy and semi-quantitative analysis was performed by Image-Pro Plus. At 6 h after heating, HSF-1 in cells cultured with normal leucine was activated and translocated from the cytosol to the nucleus, and the synthesis of HSP70 reached the maximum value and had a tendency to gather in the nucleus. However, in cells cultured with limiting leucine, HSF-1 activity decreased and accumulation of HSP70 was not found. Leucine deprivation results in the inactivation of HSF-1 leading to slight accumulation of HSP70 and no tendency to gather in the nucleus. Thus, HSF-1 may serve as a novel therapeutic target in the treatment of oral cancer.
引用
收藏
页码:2255 / 2260
页数:6
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