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. 2022 Mar 16;13(3):245. doi: 10.1038/s41419-022-04671-6

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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. 6 — A Flow cytometry data shows that LPS + EPO treatment significantly attenuates % late apoptosis (Q2 quadrant) and as a result, it increases the percentage of early apoptosis (Q3 quadrant) and the live cells (Q4 quadrant) as compared to LPS treatment. None of the treatments shows positive for necrosis. BMMØs treated with LPS (50 ng/mL) for 24 h and EPO (5 IU/mL) for 72 h. B The results of apoptosis are mentioned in the bar graph. One-way ANOVA, Tukey’s multiple comparisons test. Data were expressed as means ± SEM, ****P < 0.0001, LPS vs. LPS + EPO, n = 3.