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. 2023 Nov 23;8(4):427–442. doi: 10.1038/s41551-023-01133-y

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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. 3 — a, Left: experimental schema showing collection of RNA for whole-genome RNA-seq expression analysis, from uncloaked FS and Klg-1 mESCs, as well as cells isolated from a Klg-1-derived dormant teratoma in allogeneic FVB recipients. Right: gene expression level distribution in uncloaked FS (red), Klg-1 (green) mESCs and a Klg-1 teratoma (blue), with plot showing the proportion of genes (y axis) at a given expression level (x axis). The symbols with corresponding colours show the cloaking gene expression levels in the distributions. Vertical green dotted lines show 95–99% highest expression range. b, Antibody staining of immune factors in long-term-accepted teratomas derived in isogeneic (top) and allogeneic (bottom) settings.