Press M F, King W J
Lab Invest. 1986 Feb;54(2):188-203.
A variety of uterine cell types demonstrate endogenous peroxidase activity. Ultracytochemical localization, biochemical assays, and uterine granulocyte counts were used to characterize peroxidase activity in various regions of the human uterus and cervix during the menstrual cycle and during the postmenopausal period. Previous studies of rat uteri, using electron microscopy and biochemical assays, have shown that endometrial peroxidase is induced by estrogenic stimulation (Anderson, De Sombre, and Kang, J Cell Biol 64:668, 1975; and Biol Reprod 16:409, 1977). Tissue samples from four regions of the human uterus and one sample from the endocervix were processed for ultrastructural cytochemistry, biochemical assay, and histology. Endogenous peroxidase activity was identified with electron microscopy in the endoplasmic reticulum of endometrial epithelial cells lining four regions of the uterine cavity; the isthmus, body (2), and fundus, of some proliferative phase (2 of 6), all secretory phase (4 of 4) and all postmenopausal (3 of 3) endometria. Peroxidase activity was not demonstrable in endocervical epithelial cells. Endogenous peroxidase activity was also identified in the cytoplasmic granules of uterine eosinophils and neutrophils and in the endoplasmic reticulum of mast cells. These uterine granule-containing cells, identified with special stains in the histologic sections, were quantitated. Approximately 80% of these "uterine granulocytes" from normal uteri without intrauterine devices were neutrophils. In women of reproductive age the uterine granulocytes, although present throughout the menstrual cycle, were most numerous in the endocervix and lower uterine segment. The highest biochemical assays of peroxidase activity were also obtained in the cervix and lower uterine segment. Uterine granulocyte counts varied directly with biochemical assays of peroxidase activity indicating that they were a major determinant of biochemical peroxidase activity. Endometrial epithelial peroxidase is anatomically and temporally well placed to function as an important adjunct in maintaining a mucosal barrier to microorganisms.
多种子宫细胞类型表现出内源性过氧化物酶活性。采用超微细胞化学定位、生化分析和子宫粒细胞计数来表征月经周期和绝经后期人子宫及宫颈各区域的过氧化物酶活性。先前对大鼠子宫的研究,利用电子显微镜和生化分析,已表明子宫内膜过氧化物酶是由雌激素刺激诱导产生的(安德森、德索姆布雷和康,《细胞生物学杂志》64:668,1975;以及《生殖生物学》16:409,1977)。对人子宫四个区域的组织样本和一个宫颈内膜样本进行超微结构细胞化学、生化分析和组织学处理。通过电子显微镜在子宫腔四个区域的内膜上皮细胞内质网中鉴定出内源性过氧化物酶活性;峡部、体部(2个样本)和底部,部分增殖期(6个样本中的2个)、所有分泌期(4个样本中的4个)和所有绝经后(3个样本中的3个)的子宫内膜。在宫颈上皮细胞中未检测到过氧化物酶活性。在子宫嗜酸性粒细胞和中性粒细胞的细胞质颗粒以及肥大细胞的内质网中也鉴定出内源性过氧化物酶活性。在组织学切片中用特殊染色鉴定这些含子宫颗粒的细胞,并进行定量。来自无宫内节育器的正常子宫的这些“子宫粒细胞”中约80%为中性粒细胞。在育龄女性中,子宫粒细胞虽然在整个月经周期都存在,但在宫颈和子宫下段数量最多。过氧化物酶活性的最高生化分析结果也在宫颈和子宫下段获得。子宫粒细胞计数与过氧化物酶活性的生化分析结果直接相关,表明它们是生化过氧化物酶活性一个主要决定因素。子宫内膜上皮过氧化物酶在解剖学和时间上处于良好位置,可作为维持对微生物的黏膜屏障的重要辅助因素发挥作用。