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. 2022 Apr 19;8:209. doi: 10.1038/s41420-022-01002-8

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© The Author(s) 2022

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — A, B We separated the nucleus from the NP cells and evaluated the level of Nrf2 in the nucleus and the level of NQO1, HO-1, and SOD2 in the whole cells by western blot, treated with or without the administration of MFG-E8 with H₂O₂. C The Nrf2 was detected by immunofluorescence combined with DAPI staining for nuclei. All data are presented as mean ± standard deviation (SD), n = 6; *p < 0.01 vs. untreated group, **p < 0.01 vs. untreated group, ^##p < 0.01 vs. H₂O₂ group.