Proteinase-activated receptors in the endometrium and endometriosis
PAR₁ and PAR₂ are expressed in endometrial and endometriotic cells, where their activation promotes inflammatory cytokine production, cell proliferation, and matrix metalloproteinase activity.
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This review examines proteinase-activated receptors (PARs), focusing on PAR1 and PAR2, their expression in eutopic endometrial cells and endometriotic cells, and the proteinases that activate them, such as thrombin and tryptase. It reports that PAR1 activation in endometrial stromal cells increases vascular endothelial growth factor and matrix metalloproteinase production, and enhances plasminogen activator activities, while PAR2 activation in endometrial stromal cells stimulates IL-8 and stem cell factor production and cell proliferation. In endometriotic stromal cells, the review summarizes that PAR1 activation induces IL-8, monocyte chemotactic protein-1, and cyclooxygenase-2 with increased proliferation, and that PAR2 activation increases IL-6 and IL-8 secretion as well as cell number. As a review, the paper does not present original experiments and instead synthesizes reported findings; this paper is centrally about endometriosis — it focuses specifically on PAR1 and PAR2 functions in the endometrium and endometriotic lesions.
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Cited by (3)
- The role of decidual cells in uterine hemostasis, menstruation, inflammation, adverse pregnancy outcomes and abnormal uterine bleeding 2016
- ENMD-1068, a protease-activated receptor 2 antagonist, inhibits the development of endometriosis in a mouse model 2014
- Local hemostasis disorders underlying endometric pathology 2021
Cited by (3)
- Local hemostasis disorders underlying endometric pathology 2021
- The role of decidual cells in uterine hemostasis, menstruation, inflammation, adverse pregnancy outcomes and abnormal uterine bleeding 2016
- ENMD-1068, a protease-activated receptor 2 antagonist, inhibits the development of endometriosis in a mouse model 2014
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- europepmc
- last seen: 2026-06-13T06:22:48.782012+00:00
- openalex
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