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. 2022 Nov 8;13:6740. doi: 10.1038/s41467-022-34495-z

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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. 3 — A, B The DCs were clustered into 6 clusters according to classical markers. C The expression of function-related genes in different DC subpopulations from the control group and the CD39i treatment group. D The proportion of DC subpopulations derived from the control group and CD39i treatment group (3 subcutaneous tumors from 3 mice mixed 1:1:1). E–G There were no differences in mature, regulatory, and migration related functional gene expression after CD39i treatment. H–J. The mononuclear macrophages showed greater heterogeneity and a large number of different subpopulations, but the proportion of each subpopulation and the functional gene expression levels were not noteworthily changed after CD39i treatment.