Department of Physiology, Institute of Bioscience, University of São Paulo, São Paulo, São Paulo, Brazil.
PLoS One. 2012;7(12):e52010. doi: 10.1371/journal.pone.0052010. Epub 2012 Dec 21.
We demonstrate that during inflammatory responses the nuclear factor kappa B (NF-κB) induces the synthesis of melatonin by macrophages and that macrophage-synthesized melatonin modulates the function of these professional phagocytes in an autocrine manner. Expression of a DsRed2 fluorescent reporter driven by regions of the aa-nat promoter, that encodes the key enzyme involved in melatonin synthesis (arylalkylamine-N-acetyltransferase), containing one or two upstream κB binding sites in RAW 264.7 macrophage cell lines was repressed when NF-κB activity was inhibited by blocking its nuclear translocation or its DNA binding activity or by silencing the transcription of the RelA or c-Rel NF-κB subunits. Therefore, transcription of aa-nat driven by NF-κB dimers containing RelA or c-Rel subunits mediates pathogen-associated molecular patterns (PAMPs) or pro-inflammatory cytokine-induced melatonin synthesis in macrophages. Furthermore, melatonin acts in an autocrine manner to potentiate macrophage phagocytic activity, whereas luzindole, a competitive antagonist of melatonin receptors, decreases macrophage phagocytic activity. The opposing functions of NF-κB in the modulation of AA-NAT expression in pinealocytes and macrophages may represent the key mechanism for the switch in the source of melatonin from the pineal gland to immune-competent cells during the development of an inflammatory response.
我们证明,在炎症反应中,核因子 kappa B(NF-κB)诱导巨噬细胞合成褪黑素,而巨噬细胞合成的褪黑素以自分泌方式调节这些专业吞噬细胞的功能。在 RAW 264.7 巨噬细胞系中,由编码参与褪黑素合成的关键酶(芳基烷基胺-N-乙酰基转移酶)的 aa-nat 启动子区域驱动的 DsRed2 荧光报告基因的表达受到抑制,当 NF-κB 活性被阻止其核易位或 DNA 结合活性或沉默 RelA 或 c-Rel NF-κB 亚基的转录时。因此,由含有 RelA 或 c-Rel 亚基的 NF-κB 二聚体驱动的 aa-nat 转录介导与病原体相关的分子模式(PAMPs)或促炎细胞因子诱导的巨噬细胞中褪黑素的合成。此外,褪黑素以自分泌方式增强巨噬细胞的吞噬活性,而 luzindole 是褪黑素受体的竞争性拮抗剂,可降低巨噬细胞的吞噬活性。NF-κB 在松果体细胞和巨噬细胞中调节 AA-NAT 表达的相反功能,可能代表了在炎症反应发展过程中,褪黑素从松果腺向免疫活性细胞来源转变的关键机制。