Paper
27 October 2006 Monitoring apoptosis of TK-GFP-expressing ACC-M cells induced by ACV using FRET technique
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Proceedings Volume 6047, Fourth International Conference on Photonics and Imaging in Biology and Medicine; 60472J (2006) https://doi.org/10.1117/12.710962
Event: Fourth International Conference on Photonics and Imaging in Biology and Medicine, 2005, Tianjin, China
Abstract
Apoptosis is an evolutionary conserved cellular process that plays an important role during development, but it is also involved in tissue homeostasis and in many diseases. To study the characteristics of suicide gene system of the herpes simplex virus thymidine kinase (HSV-tk) gene in tumor cells and explore the apoptosis phenomena in this system and its effect on the human adenoid cystic carcinoma line ACC-M cell, we detected apoptosis of CD3- (ECFP-CRS-DsRed) and TK-GFP-expressing ACC-M (ACC-M-TK-GFP-CD3) cells induced by acyclovir (ACV) using fluorescence resonance energy transfer (FRET) technique. CD3 is a FRET-based indicator for activity of caspase-3, which is composed of an enhanced cyan fluorescent protein, a caspase-3 sensitive linker, and a red fluorescent protein from Discosoma with efficient maturation property. FRET from ECFP to DsRed could be detected in normal ACC-M-TK-GFP-CD3 cells, and the FRET efficient was remarkably decreased and then disappeared during the cells apoptosis induced by ACV. It was due to the activated caspase-3 cleaved the CD3 fusion protein. In this study, the results suggested that the AVC-induced apoptosis of ACC-M-TK-GFP-CD3 cells was through caspase-3 pathway.
© (2006) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Tao Xiong, Zhihong Zhang, Juqiang Lin, Jie Yang, Shaoqun Zeng, and Qingming Luo "Monitoring apoptosis of TK-GFP-expressing ACC-M cells induced by ACV using FRET technique", Proc. SPIE 6047, Fourth International Conference on Photonics and Imaging in Biology and Medicine, 60472J (27 October 2006); https://doi.org/10.1117/12.710962
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KEYWORDS
Fluorescence resonance energy transfer

Cell death

Tumors

Fluorescent proteins

Green fluorescent protein

Luminescence

Microscopy

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