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Published on: August 1, 2012
Uptake of acetyl low density lipoprotein (LDL) by stimulated canine macrophages
Y Kagawa1, E Uchida, H Nagahata
1Department of Veterinary Pathology, School of Veterinary Medicine, Rakuno Gakuen University, Hokkaido, Japan.
Insights
Canine monocytes can take up acetylated low-density lipoprotein (LDL) via scavenger receptors, differentiating into foamy macrophages. This process is crucial in the early stages of canine atherosclerosis.
Area of Science:
- Cardiovascular Research
- Immunology
- Cell Biology
Background:
- Monocytes play a role in the development of atherosclerotic lesions.
- Lipoprotein uptake by monocytes is a key event in atherogenesis.
Purpose of the Study:
- To investigate the receptor-mediated uptake of acetylated low-density lipoprotein (LDL) by canine monocytes.
- To clarify the role of monocytes in the initial stages of canine atherosclerotic lesions.
Main Methods:
- Canine peripheral blood monocytes were isolated and stimulated.
- Cells were treated with phorbol 12-myristate 13-acetate (PMA) to induce differentiation.
- Uptake of acetyl LDL and native LDL was measured.
- Inhibition studies were performed using maleyl canine serum albumin (MSA).
Main Results:
- PMA-treated canine monocytes effectively took up acetyl LDL, differentiating into foamy macrophages.
- The uptake of acetyl LDL was specifically inhibited by MSA in a dose-dependent manner.
- Canine monocytes did not exhibit uptake of native LDL under these conditions.
Conclusions:
- Canine monocytes possess a specific scavenger receptor pathway for acetyl LDL uptake.
- This receptor-mediated uptake mechanism is implicated in the early pathogenesis of canine atherosclerosis.
- Monocytes are critical players in the initiation of atherosclerotic lesion development in canines.
Abstract:
Canine monocytes from peripheral blood were stimulated by acetyl low density lipoprotein (LDL) to detect receptor-mediated uptake of lipoproteins and to clarify the role of monocytes involving in atherosclerotic lesions. Monocytes collected from peripheral blood which were treated with phorbol 12-myristate 13-acetate (PMA) took up acetyl LDL and differentiated into macrophage-like cells (foamy macrophages). Uptake of acetyl LDL was inhibited specifically by maleyl canine serum albumin (MSA) depending on its concentration. Monocytes treated with PMA did not take up native LDL. These results suggest that canine monocytes express the receptor-mediated uptake of acetyl LDL by a specific pathway (the so-called scavenger receptor) and that they play a crucial role at the initial stage of canine atherosclerotic lesions.
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