Khorram O, Garthwaite M, Magness R R
Department of Obstetrics and Gynecology, University of Wisconsin, Madison 53792, USA.
J Clin Endocrinol Metab. 1999 Jun;84(6):2226-32. doi: 10.1210/jcem.84.6.5759.
Expression of nitric oxide synthase (NOS) protein was examined by Western immunoblot analysis and immunohistochemistry in the endometrium and myometrium of 19 premenopausal and 18 postmenopausal women undergoing hysterectomy for benign gynecological reasons. The predominant isoform of NOS in the human uterus was endothelial NOS (eNOS). Using immunohistochemistry, eNOS was localized predominantly to the glandular epithelium and endometrial microvascular endothelium. eNOS was scant and inconsistently detected in endometrial stromal cells. In the myometrium, eNOS was predominantly found in smooth muscle cells (myocytes) and was also detected in the microvascular endothelium. Neuronal NOS was not detectable by immunohistochemical techniques, and inducible NOS (iNOS) was only detectable in occasional specimens, although more often in secretory specimens. iNOS, when present, was predominantly found in glandular epithelium and occasional stromal cells. Myometrial iNOS was scant and not consistently detected. By Western immunoblot analysis, neuronal NOS or iNOS was not detected. We observed a unique menstrual cycle-dependent expression of eNOS that was different in the endometrium compared to the myometrium and was independent of uterine pathology. In the endometrium, there was 62% higher expression of eNOS during the secretory phase (P = 0.00085) compared to the proliferative phase, whereas in the myometrium, there was 74% greater expression of eNOS in the proliferative phase (P = 0.03) compared to the secretory phase. Within the secretory phase, maximal endometrial eNOS expression was found in the midportion, whereas in the myometrium, highest eNOS expression occurred during the late secretory phase. In postmenopausal women not treated with hormones, a significant reduction in endometrial and myometrial expression of eNOS occurred, which was reversed by continuous hormone replacement therapy. In summary, both endogenous ovarian steroids and exogenous sex hormones influence uterine eNOS expression. Our results suggest that estrogen may regulate myometrial eNOS, whereas progesterone or a combination of estrogen and progesterone may be more important in regulating endometrial eNOS, and NO may be a critical mediator of sex steroid actions in the human uterus.
采用蛋白质免疫印迹分析和免疫组织化学方法,检测了19例因良性妇科疾病接受子宫切除术的绝经前女性和18例绝经后女性子宫内膜和肌层中一氧化氮合酶(NOS)蛋白的表达。人子宫中NOS的主要亚型是内皮型NOS(eNOS)。通过免疫组织化学方法,eNOS主要定位于腺上皮和子宫内膜微血管内皮。在子宫内膜基质细胞中,eNOS含量稀少且检测结果不一致。在肌层中,eNOS主要存在于平滑肌细胞(肌细胞)中,也可在微血管内皮中检测到。免疫组织化学技术未检测到神经元型NOS(nNOS),诱导型NOS(iNOS)仅在偶尔的标本中可检测到,不过在分泌期标本中更常见。iNOS存在时,主要见于腺上皮和偶尔的基质细胞。肌层iNOS含量稀少且检测结果不一致。通过蛋白质免疫印迹分析,未检测到nNOS或iNOS。我们观察到eNOS存在独特的月经周期依赖性表达,子宫内膜和肌层中的表达不同,且与子宫病理状态无关。在子宫内膜中,分泌期eNOS的表达比增殖期高62%(P = 0.00085),而在肌层中,增殖期eNOS的表达比分泌期高74%(P = 0.03)。在分泌期内,子宫内膜eNOS的最大表达出现在中期,而在肌层中,eNOS的最高表达出现在分泌晚期。在未接受激素治疗的绝经后女性中,子宫内膜和肌层eNOS的表达显著降低,持续激素替代疗法可使其逆转。总之,内源性卵巢类固醇和外源性性激素均影响子宫eNOS的表达。我们的结果表明,雌激素可能调节肌层eNOS,而孕酮或雌激素与孕酮的组合可能在调节子宫内膜eNOS方面更重要,一氧化氮可能是人类子宫中性类固醇作用的关键介质。