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. 2020 Oct 20;6:107. doi: 10.1038/s41420-020-00342-7

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© The Author(s) 2020

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 Murine erythroid progenitors were treated with XMD8–92 (5 μM) or vehicle control (DMSO) prior to initiation of differentiation. Levels of CD71 and Ter119 were measured by flow cytometry. Representative profiles are shown. b Mitochondrial mass was quantified in Ter119⁺CD71^high and Ter119⁺CD71^low erythroblasts using median fluorescence intensity (MFI) of MitoTracker Deep Red FM. The data represent three replicates. *P < 0.05; **P < 0.01; ***P < 0.001.