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S100A8 和 S100A9 与月经期间子宫内膜脱落有关。

S100A8 and S100A9 are associated with endometrial shedding during menstruation.

机构信息

Department of Pathology, Shizuoka General Hospital, 4-27-1 Kitaando, Aoi-ku, Shizuoka, 420-0881, Japan.

Department of Clinical Research, Shizuoka General Hospital, 4-27-1 Kitaando, Aoi-ku, Shizuoka, 420-0881, Japan.

出版信息

Med Mol Morphol. 2023 Sep;56(3):194-205. doi: 10.1007/s00795-023-00355-y. Epub 2023 Apr 22.

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.

摘要

基质金属蛋白酶(MMPs)及其主要来源——子宫内膜基质细胞(ESCs)在月经中发挥重要作用。然而,子宫内膜脱落的其他机制可能尚未被探索。本研究集中于四种蛋白质:S100A8 和 S100A9(警报素)是结合伴侣,并诱导 MMPs,MMP-3 循环依赖性地在蛋白水解级联中发挥关键作用,而 CD147 作为其配体与 S100A9 结合,诱导 MMPs。对 118 个切除标本进行了这些蛋白质的免疫染色。使用 Image J 测量和比较了每个阳性反应在 ESCs 中的百分比和位置。还检查了白细胞对 S100A8 或 S100A9 免疫阳性的影响。从经前期开始,S100A8 和 MMP-3 开始在浅层 ESCs 中重叠表达,并且在这些部位发现了 ESC 分离。S100A9 从分泌晚期开始表达,CD147 从更早开始表达。后来,S100A9 和 CD147 的表达部位包括 S100A8 的表达部位。在月经前,白细胞不会影响 S100A8 或 S100A9 的表达。这些结果表明,S100A8/S100A9 复合物在孕激素撤退时特异性地在 ESCs 中形成,诱导 MMP-3 的局部表达,并作为裂解期的开关。

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