Mapping intracellular thermal response of cancer cells to magnetic hyperthermia treatment

被引:24
|
作者
Silva, Pedro L. [1 ]
Savchuk, Oleksandr A. [1 ]
Gallo, Juan [2 ]
Garcia-Hevia, Lorena [2 ]
Banobre-Lopez, Manuel [2 ]
Nieder, Jana B. [1 ]
机构
[1] INL Int Iberian Nanotechnol Lab, Ultrafast Bio & Nanophoton Grp, P-4715330 Braga, Portugal
[2] INL Int Iberian Nanotechnol Lab, Nanomed Grp, Adv Magnet Theranost Nanostruct Lab, P-4715330 Braga, Portugal
关键词
FLUORESCENT PROTEIN GFPUV; PHOTOTHERMAL THERAPY; TEMPERATURE; THERMOMETRY; NANOPARTICLES; RELEASE;
D O I
10.1039/c9nr10370h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Temperature is a key parameter for optimal cellular function and growth. Temperature perturbation may directly lead to cell death. This can be used in cancer therapies to kill cells in tumors, a therapeutic approach called hyperthermia. To avoid overheating of tumors that may damage healthy tissues, a knowledge of the intracellular temperature reached during the hyperthermia treatment of cancer cells is relevant. Recently, several luminescent intracellular nanothermometers have been proposed; however an application to sense temperature during a hyperthermia treatment is lacking. Here we present a technique to measure intracellular temperature changes in in vitro cancer cell models. For this purpose, we study for the first time the temperature dependence of the green fluorescent protein (GFP)'s fluorescence lifetime parameter. We find the fluorescence lifetime of GFP can be used for nanothermosensing. We use GFP in a bound form to actin filaments as an intracellular thermal reporter. Furthermore, we assess intracellular temperature during in vitro magnetothermal therapy on live HeLa cells incubated with polyacrylic acidcoated iron oxide nanoparticles. Compared to other thermosensitive materials and formulations reported so far, the GFP nanothermosensor is easily expressed via transfection and various GFP variants are commercially available. We foresee that the nanothermometer developed might find widespread applications in cancer therapy research and development.
引用
收藏
页码:21647 / 21656
页数:10
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