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. 2024 Jan 31;15:945. doi: 10.1038/s41467-024-45143-z

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© The Author(s) 2024

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 7 — CCC chord diagrams displaying signaling pathways active in the perimenopausal myometrium but lost during aging, including those related to A angiogenesis (HGF), B homeostasis and tissue repair (CALCR, PERIOSTIN), C contractility (ncWNT), D immune processes (IL10, CD22, CD48) and E nervous system regulation (NGF, L1CAM). Arrows between cell types show the direction of the interactions and follow the color code of cell types commonly detected in menopause. The relative thickness of each line depicts the expression-based strength of the interaction between cell types.