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. 2020 Apr 30;11:581. doi: 10.3389/fphar.2020.00581

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Copyright © 2020 Fan, Li, Yu, Liang, Cai, Chen, Xu, Hu, Wu and Lin

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(s) 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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Effects of CSE and JPYF II on bronchial epithelial cell viability. (A, B) The MTT assay showed the effects of different concentrations of CSE at different time on BEAS-2B and 16-HBE cell viability. (C) The MTT assay showed the effects of JPYF II on BEAS-2B and 16-HBE cell viability. Results are presented by 3 independent experiments (n = 3). Values are presented as means ± SD. ^*P < 0.05, ^**P < 0.01, ^#P < 0.05 and ^##P < 0.01 compared with 0 μg/ml JPYF II group. (D) The MTT assay showed the effects of JPYF II on CSE-stimulated BEAS-2B and 16-HBE cell viability. Results are presented by three independent experiments (n = 3). Values are presented as means ± SD. ^###P < 0.001 compared with control group; ^**P < 0.01 and ^***P < 0.001 compared with CSE group.