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小鼠围产期子宫内膜和肌层中子宫单核吞噬细胞的分布与激活

Distribution and activation of uterine mononuclear phagocytes in peripartum endometrium and myometrium of the mouse.

作者信息

Mackler A M, Green L M, McMillan P J, Yellon S M

机构信息

Center for Perinatal Biology, Department of Physiology, Loma Linda University School of Medicine, Loma Linda, California 92350, USA.

出版信息

Biol Reprod. 2000 May;62(5):1193-200. doi: 10.1095/biolreprod62.5.1193.

DOI:10.1095/biolreprod62.5.1193
PMID:10775166
Abstract

The present study tested the hypothesis that macrophage distribution and activation are enhanced in the uterus before term. Mid-uterine horn tissue strips from mice on Days 15 and 18 of pregnancy, the day of birth (= Day 19), and one day postpartum were paraffin-embedded and then sectioned, stained with a monoclonal pan-macrophage marker (BM8), and processed for visualization and quantification of resident macrophages per nuclear area. Macrophages were dispersed throughout the endometrium and subluminal epithelium; cell numbers declined on the day before term, then increased postpartum. Within myometrium, macrophages congregated in stroma surrounding muscle bundles, and staining was enhanced near term. Macrophage numbers were similar in pregnant and postpartum uteri, enhanced more than 2-fold over those in nonpregnant controls. Uterine sections were also analyzed by laser-scanning cytometry to enumerate activated macrophages (i.e., those that express the intercellular adhesion molecule marker CD54+) and to determine cell cycle (propidium iodide fluorescence). Activated macrophages were directly proportional to cell numbers and, by cell cycle analysis, were not terminally differentiated. Highest cell numbers occurred on Day 15: 4-fold greater than those in nonpregnant controls and 2-fold higher than those at Day 18 or in postpartum groups. These findings indicate a decline in endometrial macrophage numbers at least one day before the onset of parturition and raise the possibility that trafficking of this immune cell may contribute to onset of labor.

摘要

本研究检验了一个假设,即足月前子宫内巨噬细胞的分布和激活会增强。对妊娠第15天和第18天、分娩日(=第19天)以及产后一天的小鼠子宫角中部组织条进行石蜡包埋,然后切片,用单克隆全巨噬细胞标志物(BM8)染色,并进行处理以可视化和定量每个核区域的常驻巨噬细胞。巨噬细胞分散在整个子宫内膜和腔上皮下;细胞数量在足月前一天下降,然后在产后增加。在子宫肌层内,巨噬细胞聚集在肌束周围的基质中,足月时染色增强。妊娠子宫和产后子宫中的巨噬细胞数量相似,比未妊娠对照组增加了2倍多。还通过激光扫描细胞术分析子宫切片,以计数活化巨噬细胞(即表达细胞间粘附分子标志物CD54+的巨噬细胞)并确定细胞周期(碘化丙啶荧光)。活化巨噬细胞与细胞数量成正比,通过细胞周期分析,它们并未终末分化。细胞数量在第15天最高:比未妊娠对照组高4倍,比第18天或产后组高2倍。这些发现表明分娩开始前至少一天子宫内膜巨噬细胞数量下降,并增加了这种免疫细胞的迁移可能促成分娩开始的可能性。

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