Uterine-derived exosomes induce the M2 polarization of macrophages via miR-210-3p/ATP5D to promote endometriosis progression
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⤵ 3 in-corpus citations
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Uterine-derived exosomes containing miR-210-3p induce M2 macrophage polarization through ATP5D, thereby promoting endometriosis progression.
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Abstract
AIMS: Endometriosis development is associated with peritoneal immune microenvironment abnormality; however, the specific mechanism is uncertain. We aimed to investigate the effects and underlying mechanisms of uterine cavity-derived exosomes on macrophage polarization and endometriosis progression.
MATERIALS AND METHODS: Uterine cavity-derived exosomes, miR-210-3p inhibitor or siATP5D were used to treat macrophages. Then evaluated the polarization of macrophages. By co-culturing of treated macrophages with endometrial stromal cells in vitro and an endometriosis C57BL6 mouse model to assess the role of uterine-derived exosomes and macrophages in the development of endometriosis.
KEY FINDINGS: Uterine cavity-derived exosomes could increase miR-210-3p expression and induce M2 macrophage polarization. Mechanistically, miR-210-3p can restrict ATP5D expression in macrophages, which leads to M2 polarization. In vivo experiments confirmed that macrophages lentivirally transduced with miR-210-3p can significantly decrease the growth and implantation of mouse endometriosis.
SIGNIFICANCE: In summary, our findings suggest that exosomes derived from the uterine cavity may drive macrophages towards M2 and promote endometriosis progression via miR-210-3p/ATP5D.
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Cited by (6)
- Do Oxidative Stress-Modified Exosomes Contribute to Infertility in Endometriosis? 2026
- Endometriosis from initiation to innovation: Immune microenvironments, clonal lesion biology, and the emerging therapeutic pipeline 2026
- Extracellular Vesicles in Endometriosis: A Comprehensive Review of Biological Insights and Methodological Challenges 2026
- Differential expression of microRNAs after induction of endometriosis in baboons† 2026
- Endometriosis as an immune-mediated disease: pathogenetic mechanisms and therapeutic strategies 2025
- SPP1 as a key modulator of M2 macrophage polarization promotes endometriosis progression via activation of the FAK/PI3K/AKT pathway: A bioinformatics and experimental study 2025
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- last seen: 2026-10-10T06:11:15.153948+00:00
- openalex
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