Probing for chemotherapy-induced peripheral neuropathy in live dorsal root ganglion neurons with atomic force microscopy

被引:24
作者
Au, Ngan Pan Bennett [1 ,2 ]
Fang, Yuqiang [3 ,4 ]
Xi, Ning [3 ,4 ]
Lai, King Wai Chiu [3 ,4 ]
Ma, Chi Him Eddie [1 ,2 ,5 ]
机构
[1] City Univ Hong Kong, Dept Biomed Sci, Hong Kong, Hong Kong, Peoples R China
[2] City Univ Hong Kong, Ctr Biosyst Neurosci & Nanotechnol, Hong Kong, Hong Kong, Peoples R China
[3] City Univ Hong Kong, Dept Mech & Biomed Engn, Hong Kong, Hong Kong, Peoples R China
[4] City Univ Hong Kong, Ctr Robot & Automat, Hong Kong, Hong Kong, Peoples R China
[5] City Univ Hong Kong, State Key Lab Marine Pollut, Hong Kong, Hong Kong, Peoples R China
关键词
AFM live cell imaging; Chemotherapy-induced peripheral neuropathy; Dorsal root ganglion neurons; Cell mechanic; Nanoindentation; CELL MECHANICS; AXONAL GROWTH; VINCRISTINE; MICROTUBULES; AFM; CYTOSKELETON; ELASTICITY; PACLITAXEL; TWEEZERS; DYNAMICS;
D O I
10.1016/j.nano.2014.03.002
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Chemotherapy-induced peripheral neuropathy (CIPN) remains a major reason for cancer patients to withdraw from their lifesaving therapy. CIPN results in irreversible sensory and motor impairments; however, the epidemiology is largely unknown. Here, we report for the first time that chemotherapy drug vincristine not only reduced axonal regeneration in primary dorsal root ganglion neuron but also induced substantial changes in cell mechanical properties detected by atomic force microscopy (AFM). Confocal imaging analysis revealed vincristine-induced microtubule depolymerization. By using AFM for high-resolution live cell imaging and quantitative analysis, we observed significant changes in cell surface roughness and stiffness of vincristine-treated neurons. Elastic modulus was decreased (21-45%) with increasing dosage of vincristine. Further study with paclitaxel, another well-known CIPN drug, confirmed the link between cell mechanics and cytoskeleton organization. These data support that our system can be used for probing potential CIPN drugs that are of enormous benefit to new chemotherapy drug development. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:1323 / 1333
页数:11
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