期刊
IMMUNOLOGY AND CELL BIOLOGY
卷 99, 期 1, 页码 84-96出版社
WILEY
DOI: 10.1111/imcb.12398
关键词
Macrophages; NFAT-5; orthodontics; salt; sodium chloride
资金
- German Research Foundation (DFG) [SCHR1622/1-1, KI2105/2-1]
Salt and compressive strain, but not tensile strain, increased the expression of NFAT-5 and most tested inflammatory factors in macrophages. NFAT-5 played a regulatory role in response to compressive strain and silencing it resulted in upregulation of IL-6 and downregulation of Ptgs-2/PG-E2 and TNF expression. Sodium accumulation in the periodontal ligament caused by dietary salt consumption might affect osteoclastogenesis and local inflammation, ultimately impacting orthodontic tooth movement.
Myeloid cells regulate bone density in response to increased salt (NaCl) intake via the osmoprotective transcription factor, nuclear factor of activated T cells-5 (NFAT-5). Because orthodontic tooth movement (OTM) is a pseudoinflammatory immunological process, we investigated the influence of NaCl and NFAT-5 on the expression pattern of macrophages in a model of simulated OTM. RAW264.7 macrophages were exposed for 4 h to 2 g cm(-2)compressive or 16% tensile or no mechanical strain (control), with or without the addition of 40 mmNaCl. We analyzed the expression of inflammatory genes and proteins [tumor necrosis factor (TNF), interleukin (IL)-6 and prostaglandin endoperoxide synthase-2 (Ptgs-2)/prostaglandin E2 (PG-E2)] by real-time-quantitative PCR and ELISA. To investigate the role of NFAT-5 in these responses, NFAT-5 was both constitutively expressed and silenced. Salt and compressive strain, but not tensile strain increased the expression of NFAT-5 and most tested inflammatory factors in macrophages. NaCl induced the expression ofPtgs-2/PG-E2 and TNF, whereas secretion of IL-6 was inhibited. Similarly, a constitutive expression of NFAT-5 reduced IL-6 expression, while increasingPtgs-2/PG-E2 and TNF expression. Silencing of NFAT-5 upregulated IL-6 and reducedPtgs-2/PG-E2 and TNF expression. Salt had an impact on the expression profile of macrophages as a reaction to compressive and tensile strain that occur during OTM. This was mediated via NFAT-5, which surprisingly also seems to play a regulatory role in mechanotransduction of compressive strain. Sodium accumulation in the periodontal ligament caused by dietary salt consumption might propagate local osteoclastogenesis via increased local inflammation and thus OTM velocity, but possibly also entail side effects such as dental root resorptions or periodontal bone loss.
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