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. 2018 Jul 24;9:1723. doi: 10.3389/fimmu.2018.01723

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Copyright © 2018 Rubio, Astudillo, Casas, Balboa and Balsinde.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Effect of lysoPlsEtn on the phagocytosis of different targets by RAW 264.7 and plasmalogen-deficient RAW.108 cells. The cells were either untreated or treated with 10 µM lysoPlsEtn or 10 µM lysoPtdEtn for 10 min as indicated. Afterward, unopsonized latex beads (5–7 particles/cell, 30-min incubation) or apoptotic Jurkat cells (ratio 3:1, 2-h incubation) were added, and phagocytosis was analyzed by flow cytometry. Measurements run in parallel using opsonized zymosan particles (OpZ, 5–7 particles/cell) are also shown for direct comparison. *Significantly different (p < 0.05) from untreated cells; **significantly different (p < 0.01) from untreated cells.