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. 2025 Aug 2.
doi: 10.1007/s10753-025-02335-z. Online ahead of print.

Large Peritoneal Macrophages Promote the Resolution of Inflammation in Injured Endometrium

Affiliations

Large Peritoneal Macrophages Promote the Resolution of Inflammation in Injured Endometrium

Jingman Li et al. Inflammation. .

Abstract

Macrophages play a significant role in the repair of endometrial injuries. While large peritoneal macrophages (LPMs) have been reported to migrate to injured organs and repair tissues within the peritoneal cavity, their involvement in the repair of injured endometrium remains unclear. In this study, we utilize a mouse model of endometrial injury that does not involve laparotomy, a procedure that typically results in a substantial loss of LPMs. Strikingly, we find that LPMs reach the endometrium within 6 h post-modeling. By depleting or supplementing LPMs, our results reveal that these cells are capable of engulfing dead cells in the endometrium and resolving inflammation. Additionally, we observe that the migration efficiency of LPMs is enhanced with increased levels of 17β-estradiol (E2) in mice. In vitro assays further confirm that E2 accelerates the migration of LPMs towards apoptotic endometrial stromal cells. Overall, our findings demonstrate that LPMs rapidly migrate into injured endometrium in relation to E2 levels and facilitate the process of tissue repair.

Keywords: 17β-estradiol; Endometrial injury; Endometrial repair; Endometrium; Large peritoneal macrophages.

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Conflict of interest statement

Declarations. Ethics Approval and Consent to Participate: The animal study was approved by Nanjing University Animal Care and Use Committee. The study was conducted inaccordance with the local legislation and institutional requirements. Patient Consent for Publication: Not applicable. Competing interests: The authors declare no competing interests.

References

    1. Wang, W., F. Vilella, P. Alama, et al. 2020. Single-cell transcriptomic atlas of the human endometrium during the menstrual cycle. Nature Medicine 26:1644–1653.
    1. Giudice, L. C. 2020. Multidimensional transcriptomic mapping of human endometrium at single-cell resolution. Nature Medicine 26:1513–1514.
    1. Lee, W. L., C. H. Liu, M. Cheng, et al. 2021. Focus on the primary prevention of intrauterine adhesions: Current concept and vision. International Journal of Molecular Sciences 22:5175.
    1. Zhou, Z., H. Wang, X. Zhang, et al. 2022. Defective autophagy contributes to endometrial epithelial-mesenchymal transition in intrauterine adhesions. Autophagy 18:2427–2442.
    1. Mouhayar, Y., J. M. Franasiak, and F. I. Sharara. 2019. Obstetrical complications of thin endometrium in assisted reproductive technologies: A systematic review. Journal of Assisted Reproduction and Genetics 36:607–611.

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