Neurite outgrowth assay

HJ Haowen Jiang
ST Sarah Jane Tiche
CH Clifford JiaJun He
MJ Mohamed Jedoui
BF Balint Forgo
MZ Meng Zhao
BH Bo He
YL Yang Li
AL Albert M. Li
AT Anh T. Truong
JH Jestine Ho
CS Cathyrin Simmermaker
YY Yanan Yang
MZ Meng-Ning Zhou
ZH Zhen Hu
DC Daniel J. Cuthbertson
KS Katrin J. Svensson
FH Florette K. Hazard
HS Hiroyuki Shimada
BC Bill Chiu
JY Jiangbin Ye
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The quantification of neurite was performed as described before [8]. Shortly, 1 × 104 SK-N-BE(2) and NB16 cells were plated in a 12 well-plate per well. After overnight incubation, cells were treated with various conditions as indicated for 72h. Then, images were taken by a Leica Florescent Microscope DMi8 in phase contrast mode (20× magnification). The lengths of the neurites were traced and quantified using the ImageJ plugin NeuronJ[15]. For each sample, total neurite length was measured and normalized to the number of cell bodies. Data are presented as mean ± SD of three biological repeats.

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