Aged garlic extract inhibits homocysteine-induced CD36 expression and foam cell formation in human macrophages

Nagatoshi Ide1, Christiane Keller, Norbert Weiss

  • 1Medical Policlinic, City Campus, University of Munich Medical Center, D-80336 Munich, Germany.

The Journal of Nutrition
|February 18, 2006
PubMed

Insights

Elevated homocysteine (Hcy) increases CD36 expression in macrophages, promoting foam cell formation. Aged garlic extract (AGE) inhibits this CD36 expression and oxidized LDL uptake, potentially modulating early atherosclerotic lesion development.

Area of Science:

  • Cardiovascular Research
  • Nutraceuticals and Atherosclerosis
  • Cell Biology and Immunology

Background:

  • Elevated plasma homocysteine (Hcy) is an independent risk factor for atherosclerotic vascular disease.
  • CD36 scavenger receptor on macrophages mediates oxidized low-density lipoprotein (OxLDL) uptake and foam cell formation, crucial in early atherosclerotic lesion development.

Purpose of the Study:

  • To investigate the effects of Hcy on CD36 expression and foam cell formation in human macrophages.
  • To evaluate the potential of aged garlic extract (AGE) in modulating these Hcy-induced changes.

Main Methods:

  • Human monocyte/macrophage (THP-1) cells were stimulated with phorbol 12-myristate 13-acetate (PMA).
  • Cells were treated with Hcy and/or AGE, and CD36 expression was quantified using flow cytometry.
  • Oxidized low-density lipoprotein (OxLDL) uptake was assessed by measuring fluorescence intensity after incubation with DiI-labeled OxLDL.

Main Results:

  • Hcy significantly increased CD36 expression on PMA-stimulated THP-1 cells.
  • AGE significantly suppressed CD36 expression, both in control conditions and in Hcy-treated cells.
  • AGE inhibited the uptake of DiI-labeled OxLDL into PMA-stimulated THP-1 cells, whereas Hcy had no significant effect on OxLDL uptake.

Conclusions:

  • Aged garlic extract (AGE) inhibits CD36 expression and oxidized low-density lipoprotein (OxLDL) uptake in macrophages.
  • These findings suggest that AGE may play a role in modulating the formation of early atherosclerotic lesions.

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