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. 2018 Apr 4;9:199. doi: 10.3389/fphar.2018.00199

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Copyright © 2018 Huang, Wang, Chen, Liu, Wang, Song, Zhang, Zhu, Huang, Liu, Song, Spencer and Yang.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Xn attenuated tau phosphorylation in both N2a/APP cells and HEK293/Tau cells. Shown are the levels of phosphorylated tau and total tau in N2a/APP cells (A,B), the levels of phosphorylated tau and total tau in HEK293/Tau cells; (C,D). The phosphorylation of upstream pathways of tau in N2a/WT and N2a/APP cells (E,F) were determined by Western-blot analysis. β-Actin was used as a loading control. N = 3. ^#p < 0.05 and ^##p < 0.01 compared to untreated N2a/APP cells, ^&p < 0.05 compared to untreated HEK293/tau cells.