Oberg F, Nilsson K
Department of Pathology, Uppsala University, University Hospital, Sweden.
Growth Factors. 1992;7(1):85-96. doi: 10.3109/08977199209023940.
Activated monocytes play an important role as producers of IL-6 during inflammation and immune response. We show that during monocytic differentiation of U-937 cells, induced by phorbolester (PMA), IL-6 mRNA expression was transiently up-regulated and IL-6 protein was secreted into the medium. In contrast, differentiation induced by VitD3 or Retinoic acid (RA) did not lead to an increase in the IL-6 expression. Thus, IL-6 expression does not seem to be associated with monocyte differentiation per se. However, U-937 cells terminally differentiated by VitD3, rapidly responded to bacterial lipopolysaccharide (LPS) induced activation by IL-6 expression and secretion. In cells, differentiated by PMA, the IL-6 expression was super-induced after activation by interferon-gamma (IFN-gamma) and LPS. The capacity of U-937 cells to respond to LPS activation by IL-6 expression was associated with the expression of CD14 and some serum components(s) were a prerequisite for a successful LPS induction. The IL-6R expression was down-regulated during monocytic differentiation of U-937 cells. In the terminally differentiated U-937 cells, the expression of IL-6R could be induced after activation by IFN-gamma and to a lesser extent by LPS, suggesting a mechanism by which activation positively regulates the response to IL-6 in macrophages.
活化的单核细胞在炎症和免疫反应中作为白细胞介素-6(IL-6)的产生者发挥重要作用。我们发现,在用佛波酯(PMA)诱导U-937细胞进行单核细胞分化过程中,IL-6信使核糖核酸(mRNA)表达短暂上调,且IL-6蛋白分泌到培养基中。相比之下,维生素D3(VitD3)或视黄酸(RA)诱导的分化并未导致IL-6表达增加。因此,IL-6表达似乎本身与单核细胞分化无关。然而,经VitD3终末分化的U-937细胞,对细菌脂多糖(LPS)诱导的激活迅速通过IL-6表达和分泌做出反应。在经PMA分化的细胞中,经干扰素-γ(IFN-γ)和LPS激活后,IL-6表达被超诱导。U-937细胞通过IL-6表达对LPS激活做出反应的能力与CD14的表达相关,并且一些血清成分是成功进行LPS诱导的先决条件。在U-937细胞的单核细胞分化过程中,IL-6受体(IL-6R)表达下调。在终末分化的U-937细胞中,经IFN-γ激活后可诱导IL-6R表达,在较小程度上经LPS也可诱导,这提示了一种激活在巨噬细胞中正向调节对IL-6反应的机制。