4.7 Article

Salt increases monocyte CCR2 expression and inflammatory responses in humans

期刊

JCI INSIGHT
卷 4, 期 21, 页码 -

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/jci.insight.130508

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资金

  1. VENI grant from ZonMW [91615052, 91619098]
  2. Netherlands Heart Foundation [2013T003, 2017T048]
  3. Dutch Kidney Foundation [KJPB 11.22, 18OKG12]
  4. ZonMW Clinical Fellowship grant [90700310]
  5. Spark-Holding BV [2015B002]
  6. European Union (ITN-grant EPIMAC)
  7. Leducq Transatlantic Network
  8. AMC-fellowship
  9. Netherlands CardioVascular Research Initiative
  10. Dutch Federation of University Medical Centers
  11. Netherlands Organization for Health Research and Development
  12. Royal Netherlands Academy of Sciences [CVON 2011-19, 2017-20]
  13. European Union (REPROGRAM [EU Horizon 2020])

向作者/读者索取更多资源

Inflammation may play a role in the link between high salt intake and its deleterious consequences. However, it is unknown whether salt can induce proinflammatory priming of monocytes and macrophages in humans. We investigated the effects of salt on monocytes and macrophages in vitro and in vivo by performing a randomized crossover trial in which 11 healthy human subjects adhered to a 2-week low-salt and high-salt diet. We demonstrate that salt increases monocyte expression of CCR2, a chemokine receptor that mediates monocyte infiltration in inflammatory diseases. In line with this, we show a salt-induced increase of plasma MCP-1, transendothelial migration of monocytes, and skin macrophage density after high-salt diet. Macrophages demonstrate signs of an increased proinflammatory phenotype after salt exposure, as represented by boosted LPS-induced cytolcine secretion of IL-6, THE, and IL-10 in vitro, and by increased HLA-DR expression and decreased CD206 expression on skin macrophages after high-salt diet. Taken together, our data open up the possibility for inflammatory monocyte and macrophage responses as potential contributors to the deleterious effects of high salt intake.

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