Low pH modulates lipopolysaccharide-induced tumor necrosis factor-alpha expression and macropinocytotic activity in

Miku Otsugu1, Ayumi Mine1, Izumi Uchida1

  • 1Laboratory of Cell Signaling Regulation, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki, Japan.

Insights

Extracellular acidification impacts macrophage inflammatory responses, increasing tumor necrosis factor-alpha (TNF-α) but altering macropinocytosis differently in foamed cells. Proton-sensing G protein-coupled receptors (GPCRs) play a role.

Area of Science:

  • Immunology
  • Cell Biology
  • Biochemistry

Background:

  • Macrophages are key players in inflammatory diseases like atherosclerosis.
  • Extracellular acidification is a hallmark of bacterial infections and atherosclerotic lesions.
  • The precise effects of acidification on macrophage inflammation and atherosclerosis remain unclear.

Purpose of the Study:

  • To investigate how extracellular acidification influences lipopolysaccharide-induced tumor necrosis factor-alpha (TNF-α) expression.
  • To examine the impact of acidification on macropinocytotic activity in RAW264.7 macrophage cells.
  • To determine the role of proton-sensing G protein-coupled receptors (GPCRs) in these processes.

Main Methods:

  • Utilized RAW264.7 cells, both un-foamed and foamed.
  • Measured TNF-α expression via real-time polymerase chain reaction.
  • Assessed macropinocytotic activity using neutral red uptake assay.
  • Investigated the involvement of proton-sensing GPCRs.

Main Results:

  • TNF-α expression significantly increased as extracellular pH decreased in both cell types.
  • Macropinocytosis was upregulated at pH 6.8 in un-foamed cells but downregulated in foamed cells.
  • Proton-sensing GPCRs were implicated in TNF-α expression and macropinocytosis in foamed cells.

Conclusions:

  • Extracellular acidification differentially modulates LPS-induced TNF-α expression and macropinocytosis in macrophages.
  • Distinct proton-sensing GPCRs mediate these varied inflammatory responses to acidification.