Kaul A K, Kumar D, Nagamani M, Goluszko P, Nowicki S, Nowicki B J
Department of Obstetrics and Gynecology, University of Texas Medical Branch at Galveston 77555-1062, USA.
Infect Immun. 1996 Feb;64(2):611-5. doi: 10.1128/iai.64.2.611-615.1996.
The mechanisms of developing infection in young, noncompromised individuals are well understood. Colonization is prerequisite for the development of infection. In human, ligands serving bacterial colonization belong to common antigens. Consequently, a majority of individuals should be sensitive to infection at all times. We hypothesize that the temporal patterns of some infections and sensitivity to them are associated with sudden changes in the density and accessibility of common receptors. Endometrial samples from women having normal menstrual cycles were examined for histological location, receptor density, and in situ hybridization of Dr (decaying-accelerating factor) ligands for Escherichia coli Dr fimbriae. Significant up-regulation and luminal expression of Dr ligands occurred during the secretory phase, whereas receptors were expressed in the basement membrane and in smaller quantities during the proliferative phase. This observation agrees with our hypotheses that some ligands recognized by bacterial adhesins change their compartmentalization and, most importantly, that they up-regulate expression at specific times.
在年轻、健康个体中发生感染的机制已得到充分了解。定植是感染发生的先决条件。在人类中,促进细菌定植的配体属于共同抗原。因此,大多数个体应随时对感染敏感。我们假设某些感染的时间模式及其敏感性与共同受体的密度和可及性的突然变化有关。对月经周期正常的女性的子宫内膜样本进行了组织学定位、受体密度以及大肠杆菌Dr菌毛的Dr(衰变加速因子)配体的原位杂交检查。Dr配体在分泌期显著上调并在管腔表达,而受体在增殖期表达于基底膜且数量较少。这一观察结果与我们的假设相符,即细菌粘附素识别的一些配体会改变其分布,最重要的是,它们会在特定时间上调表达。