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Updated: Jun 15, 2025

Using RNA-interference to Investigate the Innate Immune Response in Mouse Macrophages
Published on: November 3, 2014
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.
Abstract:
Inflammation triggers various types of diseases that need to be addressed. Macrophages play important roles in the inflammatory responses. As atherosclerosis progresses, macrophages transform into foam cells. Extracellular acidification is observed at and around bacterial infection and atherosclerotic sites. However, the effects of acidification on the inflammatory response of macrophages and the progression of atherosclerosis have not been fully understood. This study investigates the impact of extracellular acidification on lipopolysaccharide-induced tumor necrosis factor-alpha (TNF-α) expression and macropinocytotic activity in RAW264.7 cells. TNF-α expression is measured by real-time polymerase chain reaction (relative value to glyceraldehyde-3-phosphate dehydrogenase expression). Macropinocytotic activity is measured by neutral red uptake (absorbance at 540 nm). Results show that TNF-α expression increased with decreasing extracellular pH in both un-foamed and foamed cells. Macropinocytotic activity was upregulated at pH 6.8 in un-foamed cells, but downregulated in foamed cells stimulated at low pH. Proton-sensing G protein-coupled receptors (GPCRs) were involved in the expression of TNF-α and in the macropinocytotic activity of foamed cells. In conclusion, this study reveals that extracellular acidification differently affect various inflammatory responses such as LPS-induced TNF-α expression and macropinocytotic activity of RAW264.7 cells and different proton-sensing GPCRs are involved in the different inflammatory responses.
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.
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