Abstract
Native low density lipoprotein (LDL) does not affect monocyte/macrophage motility. On the other hand, oxidatively modified LDL inhibits the motility of resident peritoneal macrophages yet acts as a chemotactic factor for circulating human monocytes. We now show that lysophosphatidylcholine (lyso-PtdCho), which is generated by a phospholipase A2 activity during LDL oxidation, is a potent chemotactic factor for monocytes. It is not chemotactic for neutrophils or for resident macrophages. Platelet-activating factor, after treatment with phospholipase A2, becomes chemotactic for monocytes, whereas the intact factor is not. Synthetic 1-palmitoyl-lyso-PtdCho showed chemotactic activity comparable to that of the lyso-PtdCho fraction derived from oxidized LDL. The results suggest that lyso-PtdCho in oxidized LDL may favor recruitment of monocytes into the arterial wall during the early stages of atherogenesis. Generation of lyso-PtdCho, either from LDL itself or from membrane phospholipids of damaged cells, could play a more general role in inflammatory processes throughout the body.
Dates
Type | When |
---|---|
Created | 19 years, 3 months ago (May 31, 2006, 6:53 a.m.) |
Deposited | 3 years, 4 months ago (April 13, 2022, 12:46 p.m.) |
Indexed | 5 days, 2 hours ago (Aug. 27, 2025, 11:47 a.m.) |
Issued | 37 years, 5 months ago (April 1, 1988) |
Published | 37 years, 5 months ago (April 1, 1988) |
Published Online | 37 years, 5 months ago (April 1, 1988) |
Published Print | 37 years, 5 months ago (April 1, 1988) |
@article{Quinn_1988, title={Lysophosphatidylcholine: a chemotactic factor for human monocytes and its potential role in atherogenesis.}, volume={85}, ISSN={1091-6490}, url={http://dx.doi.org/10.1073/pnas.85.8.2805}, DOI={10.1073/pnas.85.8.2805}, number={8}, journal={Proceedings of the National Academy of Sciences}, publisher={Proceedings of the National Academy of Sciences}, author={Quinn, M T and Parthasarathy, S and Steinberg, D}, year={1988}, month=apr, pages={2805–2809} }