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. 2023 Jul 12;14(5):2152–2167. doi: 10.1002/jcsm.13292

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© 2023 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

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scRNAseq reveals multiple muscle‐resident and circulating cell types in bovine SkM. (A) UMAP graphs show unsupervised clustering of cells from all breeds and individual breeds identified by scRNAseq. (B) A heatmap shows the expression of representative marker genes used in cell‐type annotation. (C) Pie graphs show the non‐immune muscle‐resident cell type composition in all breeds and individual breeds revealed by scRNAseq. FAP, fibro/adipogenic progenitor; VEndoC, venular endothelial cell; MuC, mural cell; MC, myogenic cell; LEndoc, lymphatic endothelial cell; Mo/Ma, monocyte/macrophage.