Related Experiment Video
Updated: Jul 8, 2026

Depletion and Reconstitution of Macrophages in Mice
Published on: August 1, 2012
A moderate reduction in extracellular pH protects macrophages against apoptosis induced by oxidized low density
Andrew B Gerry1, David S Leake
1Cardiovascular Research Group, Biomolecular Sciences Section, School of Biological Sciences, University of Reading, Reading, Berkshire RG6 6AJ, United Kingdom.
Abstract:
We investigated the effect of pH on macrophage apoptosis induced by oxidized low density lipoprotein (OxLDL), as human atherosclerotic lesions have regions of low pH. Hydroperoxide-rich and oxysterol-rich LDL caused 38% and 74% apoptosis of J774 macrophages, respectively, at 24 h, as measured by the externalization of phosphatidylserine. Native LDL, however, did not cause apoptosis. Reducing the pH of the culture medium from 7.4 to 7.0 inhibited apoptosis induced by hydroperoxide-rich or oxysterol-rich OxLDL by 61% and 46%, respectively (P < 0.001). These data were confirmed by semiquantitative analysis of cytochrome c release from mitochondria. Decreasing the extracellular pH to 7.0 reduced the uptake of hydroperoxide-rich and oxysterol-rich (125)I-labeled LDL by 82% and 42%, respectively, and reduced cell surface binding of oxysterol-rich LDL by 31%. This may explain the reduced apoptosis. Additionally, low pH did not affect OxLDL-induced apoptosis of human monocytes, which do not possess scavenger receptors for OxLDL, but reduced apoptosis of human monocyte-derived macrophages, which do possess them. Our investigations suggest that the presence of areas of low pH within atherosclerotic lesions may reduce the uptake of OxLDL and reduce macrophage apoptosis, thus affecting lesion progression.
Insights
Low pH environments in atherosclerotic lesions reduce oxidized low-density lipoprotein (OxLDL) uptake and macrophage apoptosis. This finding suggests a mechanism influencing the progression of atherosclerosis.
Area of Science:
- Biochemistry
- Cell Biology
- Pathophysiology
Background:
- Human atherosclerotic lesions contain regions with low pH.
- Oxidized low-density lipoprotein (OxLDL) plays a role in the development of atherosclerosis.
- Macrophage apoptosis is a key process in atherosclerotic plaque development.
Purpose of the Study:
- To investigate the impact of pH on OxLDL-induced macrophage apoptosis.
- To explore the relationship between extracellular pH, OxLDL uptake, and macrophage cell death.
Main Methods:
- J774 macrophages and human monocytes/macrophages were cultured under varying pH conditions.
- Apoptosis was measured by phosphatidylserine externalization and cytochrome c release.
- OxLDL uptake and cell surface binding were quantified using radiolabeled LDL.
Main Results:
- Hydroperoxide-rich and oxysterol-rich OxLDL induced significant macrophage apoptosis at pH 7.4.
- Reducing the pH to 7.0 markedly inhibited OxLDL-induced apoptosis (61% and 46% reduction).
- Low pH decreased OxLDL uptake by macrophages (82% and 42% reduction) and cell surface binding.
Conclusions:
- Extracellular pH significantly modulates OxLDL-induced macrophage apoptosis.
- Reduced OxLDL uptake at lower pH may explain the decreased apoptosis.
- Low pH in atherosclerotic lesions might limit OxLDL accumulation and macrophage apoptosis, impacting lesion progression.
Related Concept Videos
Phagocytosis of Apoptotic Cells
Normal cells contain receptors that prevent them from being recognized by phagocytes.
The Extrinsic Apoptotic Pathway
Inflammation
Apoptosis
Cellular Injury V: Apoptosis and Autophagy

