Liu R, O'Connell M, Johnson K, Pritzker K, Mackman N, Terkeltaub R
Department of Veterans Affairs Medical Center, University of California, San Diego 92161, USA.
Arthritis Rheum. 2000 May;43(5):1145-55. doi: 10.1002/1529-0131(200005)43:5<1145::AID-ANR25>3.0.CO;2-T.
Monosodium urate monohydrate (MSU) and calcium pyrophosphate dihydrate (CPPD) crystals cause acute gout and pseudogout, respectively. Because acute gout and pseudogout appear to be dependent on interleukin-8 (IL-8)-induced neutrophil ingress, this study was undertaken to define and compare how MSU and CPPD crystals stimulate IL-8 messenger RNA (mRNA) expression in mononuclear phagocytes.
MSU and CPPD crystal-induced mitogen-activated protein kinase (MAPK) signal transduction and IL-8 transcriptional activation were studied in human monocytic cells, using the THP-1 cell line.
MSU and CPPD crystals (0.5 mg/ml) induced activation of c-Jun N-terminal kinase, extracellular signal-regulated kinase 1 (ERK-1)/ERK-2, and p38 MAPK pathways in THP-1 cells. Activation of the ERK-1/ERK-2 pathway was essential for MSU and CPPD crystal-induced IL-8 mRNA expression, whereas the p38 pathway played a greater role in IL-8 mRNA expression in response to CPPD crystals in comparison with MSU crystals. Both crystals induced the binding of nuclear factor kappaB (NF-kappaB), including the NF-kappaB complex c-Rel/RelA, and activator protein 1 (AP-1, including N-terminal phosphorylated c-Jun) to the IL-8 promoter. Both crystals induced transcriptional activation of the IL-8 promoter, which was dependent on activation of c-Rel/RelA and AP-1. Activation of the NF-IL-6 transcription factor played a lesser role. Finally, crystal-induced IL-8 promoter activation was mediated by activation of the ERK-1/ERK-2 pathway, as demonstrated by transfection of dominant-negative raf-1.
These results indicate that ERK-1/ ERK-2 signaling and transcriptional activation through AP-1 and NF-kappaB are essential for the induction of IL-8 expression in mononuclear phagocytes in response to CPPD and MSU crystals.
尿酸单钠一水合物(MSU)和二水焦磷酸钙(CPPD)晶体分别引发急性痛风和假性痛风。由于急性痛风和假性痛风似乎依赖于白细胞介素-8(IL-8)诱导的中性粒细胞浸润,因此开展本研究以明确并比较MSU和CPPD晶体如何刺激单核吞噬细胞中IL-8信使核糖核酸(mRNA)的表达。
使用THP-1细胞系,在人单核细胞中研究MSU和CPPD晶体诱导的丝裂原活化蛋白激酶(MAPK)信号转导及IL-8转录激活。
MSU和CPPD晶体(0.5mg/ml)诱导THP-1细胞中c-Jun氨基末端激酶、细胞外信号调节激酶1(ERK-1)/ERK-2和p38 MAPK通路的激活。ERK-1/ERK-2通路的激活对于MSU和CPPD晶体诱导的IL-8 mRNA表达至关重要,而与MSU晶体相比,p38通路在响应CPPD晶体时对IL-8 mRNA表达发挥更大作用。两种晶体均诱导核因子κB(NF-κB,包括NF-κB复合物c-Rel/RelA)和活化蛋白1(AP-1,包括氨基末端磷酸化的c-Jun)与IL-8启动子结合。两种晶体均诱导IL-8启动子的转录激活,这依赖于c-Rel/RelA和AP-1的激活。NF-IL-6转录因子的激活作用较小。最后,如通过转染显性负性raf-1所证明,晶体诱导的IL-8启动子激活由ERK-1/ERK-2通路的激活介导。
这些结果表明,ERK-1/ERK-2信号传导以及通过AP-1和NF-κB的转录激活对于单核吞噬细胞响应CPPD和MSU晶体诱导IL-8表达至关重要。