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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. 8 — A Flow cytometry gating strategy of dual staining (CD11b + CD206⁺), where that shows (P4, histogram) EPO treatment (5000 IU/kg/IP, immediately after surgery and on post-surgery day 1 and 2) significantly augments percent phagocytosis of intraperitoneally injected apoptotic SNSCs (PKH26 labeled) as compared to saline treatment (normal saline, 0.1 ml/IP/mouse) and the results are denoted in the bar graph (B). C Flow cytometry data shows EPO significantly recruits PMØs (CD11b + F4/80⁺) following intraperitoneal injection of apoptotic SNSCs (PKH26 labeled) as compared to saline treatment and the results are denoted in the bar graph (D). Unpaired t-tests. Data were expressed as means ± SEM, #P < 0.05, Saline vs. EPO, n = 3/group.