Tabibzadeh S, Kong Q F, Babaknia A
Department of Pathology, University of South Florida Health Sciences Center, Tampa 33612.
J Clin Endocrinol Metab. 1994 Oct;79(4):1024-32. doi: 10.1210/jcem.79.4.7962270.
In the present study, we examined the pattern of expression of human leukocyte antigen (HLA)-DR as well as several adhesion molecules implicated in leukocyte trafficking, including ICAM-1, E-selectin, and VCAM-1 in human endometrium. All of the vessels in endometrium exhibited HLA-DR and ICAM-1 throughout the menstrual cycle. In the proliferative phase, endothelial cells in the functionalis were weak to nonreactive for VCAM-1 and were E-selectin negative (E-selectin-). Endothelial cells of the vessels in the basalis and within myometrium were VCAM positive (VCAM-1+)/E-selectin-. In sharp contrast, in the secretory phase, endothelial cells in the basalis were VCAM-1+/E-selectin+. Surprisingly, endometrial glands, primarily those in the basalis, expressed E-selectin and VCAM-1 during the entire menstrual cycle. Stromal cells were ICAM-1+ and were focally HLA-DR+ around HLA-DR+ lymphoid cells during the entire menstrual cycle and were E-selectin-/VCAM-1- during the proliferative phase. Immunoreactivity for VCAM-1 and E-selectin, however, appeared in the stromal cells in the upper functionalis in the secretory phase. Immunoreactivity for VCAM-1 was the distinguishing feature that separated the lymphoid cells in the aggregates from other nonaggregated lymphoid cells. Recruitment of leukocytes to tissues is in part due to cytokine-regulated expression of specific molecules on endothelial cells. Therefore, we tested the effects of cytokines on the expression of these molecules in endothelial cells derived from microvasculature. ICAM-1 and VCAM-1 were inducible in a dose-dependent fashion in the endothelial cells by interleukin-1 alpha (IL-1 alpha), interferon-gamma (IFN gamma), and tumor necrosis factor-alpha (TNF alpha). Expression of HLA-DR in endothelial cells was inducible by IL-1 alpha and IFN gamma and not by TNF alpha. Expression of E-selectin on endothelial cells was induced only by IL-1 alpha, not by IFN gamma or TNF alpha. Cytokine treatment of endothelial cells significantly enhanced the binding of leukocytes to endothelial cells. The data show a heterogeneity in the vasculature of endometrium with respect to the expression of various adhesion molecules. This heterogeneity is potentially related to the type or amount of cytokine with which endothelial cells are activated. In addition, unique cell- and site-specific expression of adhesion molecules in human endometrium throughout the menstrual cycle may account for the distinct distribution pattern of leukocytes in this tissue.
在本研究中,我们检测了人子宫内膜中人类白细胞抗原(HLA)-DR以及几种与白细胞转运相关的黏附分子的表达模式,这些黏附分子包括细胞间黏附分子-1(ICAM-1)、E-选择素和血管细胞黏附分子-1(VCAM-1)。在整个月经周期中,子宫内膜中的所有血管均表达HLA-DR和ICAM-1。在增殖期,功能层的内皮细胞对VCAM-1呈弱阳性至无反应,且E-选择素阴性(E-选择素-)。基底层和肌层内血管的内皮细胞VCAM阳性(VCAM-1+)/E-选择素-。与之形成鲜明对比的是,在分泌期,基底层的内皮细胞VCAM-1+/E-选择素+。令人惊讶的是,子宫内膜腺体,主要是基底层的腺体,在整个月经周期中均表达E-选择素和VCAM-1。基质细胞在整个月经周期中ICAM-1+,且在HLA-DR+淋巴细胞周围局部HLA-DR+,在增殖期为E-选择素-/VCAM-1-。然而,在分泌期,功能层上部的基质细胞出现了VCAM-1和E-选择素的免疫反应性。VCAM-1的免疫反应性是将聚集的淋巴细胞与其他非聚集淋巴细胞区分开来的显著特征。白细胞向组织的募集部分归因于细胞因子调节内皮细胞上特定分子的表达。因此,我们测试了细胞因子对源自微血管的内皮细胞中这些分子表达的影响。ICAM-1和VCAM-1可被白细胞介素-1α(IL-1α)、干扰素-γ(IFNγ)和肿瘤坏死因子-α(TNFα)以剂量依赖性方式诱导内皮细胞表达。内皮细胞中HLA-DR的表达可被IL-1α和IFNγ诱导,而不能被TNFα诱导。内皮细胞上E-选择素的表达仅由IL-1α诱导,而不能被IFNγ或TNFα诱导。细胞因子处理内皮细胞显著增强了白细胞与内皮细胞的结合。数据显示,子宫内膜血管系统在各种黏附分子的表达方面存在异质性。这种异质性可能与激活内皮细胞的细胞因子类型或数量有关。此外,人子宫内膜在整个月经周期中黏附分子独特的细胞和位点特异性表达可能解释了该组织中白细胞的独特分布模式。