Riley S C, Walton J C, Herlick J M, Challis J R
Department of Obstetrics and Gynecology, Lawson Research Institute, University of Western Ontario, St. Joseph's Health Centre, London, Canada.
J Clin Endocrinol Metab. 1991 May;72(5):1001-7. doi: 10.1210/jcem-72-5-1001.
Using immunohistochemical techniques, we have determined the localization and distribution of CRH immunoreactivity (CRH-IR) in the human placenta, fetal membranes, decidua, and umbilical cord. Tissues were obtained at 6-8 weeks of pregnancy, at term, in association with premature birth, and from patients with pregnancy-induced hypertension or diabetes mellitus. A polyclonal antibody to the epithelial cell marker cytokeratin was used to identify trophoblast cells. CRH-IR was not detected in placenta or decidua at 6-8 weeks gestation. In tissues obtained after idiopathic premature delivery after 21 weeks gestation, positive CRH staining was found in placenta in syncytiotrophoblast and intermediate trophoblast, but not cytotrophoblast. CRH-IR was present in intermediate trophoblast cells that had invaded maternal blood vessels in decidua basalis. In the fetal membranes, CRH-IR was localized in the epithelium and subepithelial cells of amnion, in the trophoblast layer, in some cells of the reticular and cellular layers of chorion, and in some stromal cells and invasive trophoblast cells of decidua. CRH-IR was found in the amniotic epithelium of the umbilical cord and in the musculature of the umbilical vessels. This pattern of distribution of CRH-IR was found in tissues from 21 weeks gestation to term and postterm, and was similar in tissues examined from patients with pregnancy-induced hypertension and diabetes mellitus. These results show clearly that in placenta and membranes, CRH is localized primarily to syncytiotrophoblast and intermediate trophoblast, but not to cytotrophoblast cells. We suggest that the localization of CRH-IR is consistent with CRH affecting paracrine/autocrine interactions within the placenta, fetal membranes, and decidua that may be involved in the maturation of the fetal hypothalamic-pituitary-adrenal axis and in the stimulus and maintainance of labor.
运用免疫组织化学技术,我们已确定促肾上腺皮质激素释放激素免疫反应性(CRH-IR)在人胎盘、胎膜、蜕膜及脐带中的定位与分布。组织取自妊娠6-8周、足月、早产相关情况以及妊娠高血压或糖尿病患者。使用针对上皮细胞标志物细胞角蛋白的多克隆抗体来识别滋养层细胞。妊娠6-8周时,在胎盘或蜕膜中未检测到CRH-IR。在妊娠21周后特发性早产获取的组织中,在胎盘的合体滋养层和中间滋养层发现CRH阳性染色,但细胞滋养层未发现。CRH-IR存在于侵入基蜕膜母体血管的中间滋养层细胞中。在胎膜中,CRH-IR定位于羊膜的上皮和上皮下细胞、滋养层、绒毛膜网状层和细胞层的一些细胞以及蜕膜的一些基质细胞和侵入性滋养层细胞中。在脐带的羊膜上皮和脐血管的肌肉组织中发现了CRH-IR。从妊娠21周直至足月及过期妊娠的组织中均发现这种CRH-IR的分布模式,并且在妊娠高血压和糖尿病患者检查的组织中类似。这些结果清楚地表明,在胎盘和胎膜中,CRH主要定位于合体滋养层和中间滋养层,而非细胞滋养层细胞。我们认为,CRH-IR的定位与CRH影响胎盘、胎膜和蜕膜内的旁分泌/自分泌相互作用一致,这可能参与胎儿下丘脑-垂体-肾上腺轴的成熟以及分娩的刺激和维持。