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. 2021 May 26;12:300. doi: 10.1186/s13287-021-02375-w

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 5 — Apol8-NSC transplantation promotes improvement in motor function and electrophysiological recovery after SCI. a Representative functional recovery of animals in the SCI group, LOCS+NSCs group, and LOCS+Apol8-NSCs group at 8 weeks after SCI. b BMS scores of mice in each group at 8 weeks post-injury. c Motor evoked potential (MEP) results of LOCS+NSCs and LOCS+Apol8-NSCs treatment group mice at 8 weeks post-treatment. d, e Latent periods and amplitude ratio of MEP in LOCS+NSCs and LOCS+Apol8-NSCs treatment group mice, respectively. Error bars represent the mean ± SD