Semer D, Reisler K, MacDonald P C, Casey M L
Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas 75235-9051.
Ann N Y Acad Sci. 1991;622:99-110. doi: 10.1111/j.1749-6632.1991.tb37854.x.
Cytokines are known to act in a variety of tissues, most commonly in a paracrine manner, to effect a number of biochemical processes. Previously, we found that human endometrial stromal cells respond to the action of interleukin-1 (IL-1) with an increase in the production of prostaglandins. In these investigations, we also found that IL-1 acts in endometrial stromal cells to stimulate the synthesis of IL-1 and IL-6 mRNA and protein. Specifically, in human endometrial stromal cells maintained in monolayer culture, treatment with IL-1 alpha leads to a striking increase in the synthesis of IL-1 beta mRNA and protein; this increase is IL-1 alpha-dose- and time-dependent. The pro-IL-1 beta produced, however, is not secreted into the culture medium but is retained within the stromal cell. The failure of secretion of IL-1 beta is characteristic of non-monocyte/macrophage cell types; this obtains because the enzyme that effects processing of pro-IL-1 beta (31 kDa) to the mature, secreted form of IL-1 beta (17 kDa) is believed to be present only in monocytes/macrophages. We also find that IL-1 and tumor necrosis factor-alpha (TNF-alpha) act in endometrial stromal cells to stimulate the synthesis of interleukin-6 (IL-6) mRNA and protein; the IL-6 produced by these cells is secreted into the culture medium. In addition, we find that IL-1 acts in endometrial stromal cells to inhibit the expression of mRNA for connexin43, a gap junction protein that is believed to be the principal component of gap junctions in cardiac and smooth muscle. Thus, it is likely that IL-1 action leads to a decrease in gap junction-dependent intercellular communication among endometrial stromal cells. Based on these findings, we conclude that endometrial stromal cells are responsive to the actions of IL-1 and TNF-alpha. These cells synthesize both IL-1 and IL-6; and, IL-6 is released into the extracellular medium. Thus, the possibility exists that the synthesis and action of cytokines may be involved in the mechanisms that serve to regulate the mesenchymal-epithelial interactions between endometrial stromal and glandular components; and, the formation and action of cytokines in decidua may serve to modulate immunological and infectious challenges encountered by this tissue in pregnancy.
已知细胞因子作用于多种组织,最常见的是以旁分泌方式影响许多生化过程。此前,我们发现人子宫内膜基质细胞对白细胞介素 -1(IL-1)的作用会产生前列腺素生成增加的反应。在这些研究中,我们还发现IL-1作用于子宫内膜基质细胞以刺激IL-1和IL-6 mRNA及蛋白质的合成。具体而言,在单层培养的人子宫内膜基质细胞中,用IL-1α处理会导致IL-1β mRNA和蛋白质的合成显著增加;这种增加是IL-1α剂量和时间依赖性的。然而,所产生的前体IL-1β不会分泌到培养基中,而是保留在基质细胞内。IL-1β不分泌是非单核细胞/巨噬细胞类型的特征;这是因为据信将前体IL-1β(31 kDa)加工成成熟的、分泌形式的IL-1β(17 kDa)的酶仅存在于单核细胞/巨噬细胞中。我们还发现IL-1和肿瘤坏死因子 -α(TNF-α)作用于子宫内膜基质细胞以刺激白细胞介素 -6(IL-6)mRNA和蛋白质的合成;这些细胞产生的IL-6会分泌到培养基中。此外,我们发现IL-1作用于子宫内膜基质细胞以抑制连接蛋白43(connexin43)的mRNA表达,连接蛋白43是一种间隙连接蛋白,被认为是心脏和平滑肌中间隙连接的主要成分。因此,IL-1的作用可能导致子宫内膜基质细胞之间依赖间隙连接的细胞间通讯减少。基于这些发现,我们得出结论,子宫内膜基质细胞对IL-1和TNF-α的作用有反应。这些细胞合成IL-1和IL-6;并且,IL-6释放到细胞外介质中。因此,细胞因子的合成和作用可能参与调节子宫内膜基质和腺体成分之间间充质 - 上皮相互作用的机制;并且,蜕膜中细胞因子的形成和作用可能有助于调节该组织在妊娠期间遇到的免疫和感染挑战。