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. 2023 Jun 13;6:638. doi: 10.1038/s42003-023-05011-w

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© The Author(s) 2023

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 UMAPs of aggregate human omental fat showing BMPER is expressed in the PDGFRA⁺ population. b UMAPs of aggregate mouse perigonadal fat showing Bmper is expressed in the Pdgfra⁺ population. c Relative mRNA expression of Bmper in mature adipocytes, lineage^- (Lin^-), and Lin⁺ SVF isolated from epididymal white adipose tissue of male C57BL6/J control mice. d Relative mRNA expression of Bmper in undifferentiated visceral APCs from female or male mice. e Immunohistochemistry staining for Bmper (green), Golgin-97 (red), or Dapi (blue) in undifferentiated visceral APCs from female or male mice. Values are means ± SD. n = two independent experiments in (c) and n = 6 in (d).