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.

Journal of Lipid Research
|January 19, 2008
PubMed

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.

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