S100A8 and S100A9 are associated with endometrial shedding during menstruation.

IF 1.2 4区 医学 Q3 PATHOLOGY
Medical Molecular Morphology Pub Date : 2023-09-01 Epub Date: 2023-04-22 DOI:10.1007/s00795-023-00355-y
Kazumori Arai, Aki Kubota, Tomohiro Iwasaki, Akihiro Sonoda, Junichi Sakane
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引用次数: 0

Abstract

Matrix metalloproteinases (MMPs) and their major source, endometrial stromal cells (ESCs), play important roles in menstruation. However, other mechanisms in endometrial shedding may be unexplored. This study focused on four proteins: S100A8 and S100A9 (alarmins) are binding partners and induce MMPs, MMP-3 cycle-dependently plays a key role in the proteolytic cascade, and CD147, which has S100A9 as its ligand, induces MMPs. Immunostaining for these proteins was performed on 118 resected specimens. The percentage and location of each positive reaction in ESCs were measured and compared using Image J. The influence of leukocytes on S100A8 or S100A9 immunopositivity was also examined. From the premenstrual phase, S100A8 and MMP-3 began to have overlapping expressions in ESCs of the superficial layer, and ESC detachment was found within these sites. S100A9 was expressed from the late secretory phase and CD147 already from earlier. Later, the expression sites of S100A9 and CD147 included those of S100A8. Before menstruation, S100A8 or S100A9 expression was not affected by leukocytes. These results suggest that the local formation of S100A8/S100A9 complex, which occurs specifically in ESCs upon progesterone withdrawal, induces the local expression of MMP-3 and serves as a switch to the lysis phase.

Abstract Image

S100A8和S100A9与月经期间子宫内膜脱落有关。
基质金属蛋白酶(MMPs)及其主要来源子宫内膜基质细胞(ESCs)在月经中起着重要作用。然而,子宫内膜脱落的其他机制可能尚未探索。本研究主要关注四种蛋白:S100A8和S100A9(报警蛋白)是结合伙伴并诱导MMPs, MMP-3周期依赖性在蛋白水解级联中起关键作用,CD147以S100A9为配体诱导MMPs。对118个切除标本进行了这些蛋白的免疫染色。利用图像j测量和比较ESCs中各阳性反应的百分比和位置,并检测白细胞对S100A8或S100A9免疫阳性的影响。从经前期开始,S100A8和MMP-3在浅层ESCs中开始重叠表达,并在这些部位发现ESC脱离。S100A9在分泌后期表达,CD147在分泌早期表达。随后,S100A9和CD147的表达位点包含了S100A8的表达位点。月经前,S100A8和S100A9的表达不受白细胞的影响。这些结果表明,S100A8/S100A9复合物的局部形成,特别是在黄体酮退出后发生在ESCs中,诱导MMP-3的局部表达,并作为裂解阶段的开关。
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来源期刊
Medical Molecular Morphology
Medical Molecular Morphology 医学-病理学
CiteScore
2.90
自引率
5.60%
发文量
30
审稿时长
>12 weeks
期刊介绍: Medical Molecular Morphology is an international forum for researchers in both basic and clinical medicine to present and discuss new research on the structural mechanisms and the processes of health and disease at the molecular level. The structures of molecules, organelles, cells, tissues, and organs determine their normal function. Disease is thus best understood in terms of structural changes in these different levels of biological organization, especially in molecules and molecular interactions as well as the cellular localization of chemical components. Medical Molecular Morphology welcomes articles on basic or clinical research in the fields of cell biology, molecular biology, and medical, veterinary, and dental sciences using techniques for structural research such as electron microscopy, confocal laser scanning microscopy, enzyme histochemistry, immunohistochemistry, radioautography, X-ray microanalysis, and in situ hybridization. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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