Donnelly R P, Levine J, Hartwell D Q, Frendl G, Fenton M J, Beller D I
Laboratory of Immunology, Evans Memorial Department of Clinical Research, University Hospital, Boston, MA 02118.
J Immunol. 1990 Nov 15;145(10):3231-9.
IL-1 is a multifunctional, immunoregulatory polypeptide produced by many cell types. Because activated macrophages are a major source of IL-1 and have also been implicated in the pathogenesis of autoimmune disease, we investigated the regulation of IL-1 expression in several autoimmune-prone strains of mice. Peritoneal macrophages derived from the autoimmune-prone strains MRL/lpr, MRL/+, NZB, and NZB/W F1, as well as NZW, displayed transient expression of IL-1 in contrast to the stable expression characteristic of control normal strains including A. Thy, A/J, B10, B10.A, B10.D2, C57BL/6, BALB/c, and C3H/HeN. The down-regulation of IL-1 by macrophages from the autoimmune-prone mice was not attributable to inherently defective signal transduction because macrophages from both the normal and autoimmune-prone strains displayed substantial initial levels of cell-associated and secreted IL-1. However, during the first 2 to 3 days in culture, macrophages from autoimmune-prone mice became progressively refractory to both induction and maintenance of IL-1, a pattern that correlated with changes in the levels of IL-1 alpha and beta mRNA. The progressive reduction in IL-1 expression by macrophages from these autoimmune-prone strains was not due to a reduction in general metabolism or viability, because expression of cell surface antigens, including MHC class I and II Ag and LFA-1, was comparable to that of control macrophages. Because IL-1 plays a critical role in the homeostasis of a variety of cell lineages, defective expression, and maintenance of IL-1 (and perhaps other cytokines) by macrophages from the autoimmune-prone strains may contribute to the immune dysregulation that develops in these mice. Alternatively, cytokine dysregulation might not contribute directly to disease, but rather reflect a more basic defect related to specific signal transducing or gene regulatory pathways.
白细胞介素-1(IL-1)是一种由多种细胞类型产生的多功能免疫调节多肽。由于活化的巨噬细胞是IL-1的主要来源,并且也与自身免疫性疾病的发病机制有关,我们研究了几种易患自身免疫性疾病的小鼠品系中IL-1表达的调控。来自易患自身免疫性疾病的品系MRL/lpr、MRL/+、NZB和NZB/W F1以及NZW的腹腔巨噬细胞,与包括A.Thy、A/J、B10、B10.A、B10.D2、C57BL/6、BALB/c和C3H/HeN等对照正常品系的稳定表达特征相比,显示出IL-1的瞬时表达。易患自身免疫性疾病小鼠的巨噬细胞对IL-1的下调并非归因于内在的信号转导缺陷,因为正常品系和易患自身免疫性疾病品系的巨噬细胞都显示出大量初始水平的细胞相关和分泌型IL-1。然而,在培养的最初2至3天内,易患自身免疫性疾病小鼠的巨噬细胞对IL-1的诱导和维持逐渐变得不敏感,这种模式与IL-1α和β mRNA水平的变化相关。这些易患自身免疫性疾病品系的巨噬细胞对IL-1表达的逐渐降低并非由于一般代谢或活力的降低,因为包括MHC I类和II类抗原以及淋巴细胞功能相关抗原-1(LFA-1)在内的细胞表面抗原的表达与对照巨噬细胞相当。由于IL-1在多种细胞谱系的稳态中起关键作用,易患自身免疫性疾病品系的巨噬细胞对IL-1(可能还有其他细胞因子)的表达和维持缺陷可能导致这些小鼠发生免疫失调。或者,细胞因子失调可能不会直接导致疾病,但而是反映了与特定信号转导或基因调控途径相关的更基本缺陷。