Berkova N, Lemay A, Dresser D W, Fontaine J Y, Kerizit J, Goupil S
Laboratoire d'endocrinologie de la reproduction, Centre de recherche de St-Francioise d'Assise, Centre Hospitalier Universitaire de Québec (CHUQ), Pavillon Saint-Franciois d'Assise 10, Québec (Québec) G1L 3L5, Canada.
Mol Hum Reprod. 2001 Aug;7(8):747-54. doi: 10.1093/molehr/7.8.747.
Assuming that haptoglobin, by virtue of its immunomodulatory properties, could be a regulatory factor during reproduction, its presence in the human uterus was determined. Protein extracts from endometrial tissue samples of pregnant and non-pregnant women were analysed by the immunoblot technique and the intensities of specific bands were quantified. Bands corresponding to haptoglobin were identified in tissue samples obtained from both sources. Protein, purified by high-performance liquid chromatography and monitored by Western blot analysis for its haptoglobin identity, was used for amino-terminal sequencing. Sequencing of the 42 kDa protein identified it as the beta chain of haptoglobin. Immunohistochemistry was used to corroborate the findings and to visualize the distribution of haptoglobin in the tissue. The intensity of the 42 kDa band derived from decidua graviditatis was significantly higher than the intensity of bands derived from non-pregnant endometrium in the proliferative phase (P < 0.01) and in the secretory phase (P < 0.05). Immunohistochemical staining with anti-human haptoglobin antibody elicited strong signals in the decidua graviditatis and weaker signals in the normal endometrium, with the latter showing menstrual cycle-dependent variation. Moderate staining of stroma and a lack of staining of epithelium in the proliferative phase contrasted with the strong staining of stroma and moderate level of staining of epithelium observed in the secretory phase. Haptoglobin in the uterus may exert several functions such as the known binding of haemoglobin, but could also be involved in the multi-factorial mechanism protecting the fetus from a maternal allograft-like immune response.
鉴于触珠蛋白因其免疫调节特性可能在生殖过程中作为一种调节因子,因此对其在人子宫中的存在情况进行了测定。采用免疫印迹技术分析了孕妇和非孕妇子宫内膜组织样本的蛋白质提取物,并对特定条带的强度进行了定量。在从这两种来源获得的组织样本中均鉴定出了与触珠蛋白相对应的条带。通过高效液相色谱法纯化并经蛋白质印迹分析监测其触珠蛋白身份的蛋白质用于氨基末端测序。对42 kDa蛋白质的测序确定其为触珠蛋白的β链。采用免疫组织化学法来证实这些发现并观察触珠蛋白在组织中的分布情况。来自妊娠蜕膜的42 kDa条带的强度显著高于增殖期(P < 0.01)和分泌期(P < 0.05)非妊娠子宫内膜条带的强度。用抗人触珠蛋白抗体进行免疫组织化学染色时,妊娠蜕膜中产生强信号,正常子宫内膜中产生较弱信号,后者呈现月经周期依赖性变化。增殖期基质染色中等而上皮无染色,与之形成对比的是,分泌期观察到基质强染色而上皮中等程度染色。子宫中的触珠蛋白可能发挥多种功能,如已知的血红蛋白结合功能,但也可能参与保护胎儿免受母体同种异体移植样免疫反应的多因素机制。