Abstract
Low concentrations of oxidized low density lipoprotein (OxLDL) are cytoprotective for phagocytes, although the underlying mechanisms remain unclear. We investigated signaling pathways used by OxLDL to attenuate apoptosis in monocytic cells. OxLDL at 25-50 μg/ml inhibited staurosporine-induced apoptosis in THP-1 cells and mouse peritoneal macrophages, and it was cytoprotective in human primary monocytes upon serum withdrawal. Attenuated cell demise was reversed by blocking extracellular signal-regulated kinase (ERK) signaling. Translocation of cytochrome c to the cytosol was attenuated by OxLDL, which again demanded ERK signaling. Analysis of Bcl-2 family proteins revealed phosphorylation of Bad at serine 112 as well as ERK-dependent inhibition of Mcl-1 degradation. Although the formation of reactive oxygen species (ROS) is an established signal generated by OxLDL, ROS scavengers did not interfere with cell protection by OxLDL. Thus, activation of the ERK signaling pathway by OxLDL is important to protect phagocytes from apoptosis. Copyright ©2008 by the American Society for Biochemistry and Molecular Biology, Inc.
Author supplied keywords
Cite
CITATION STYLE
Namgaladze, D., Kollas, A., & Brüne, B. (2008). Oxidized LDL attenuates apoptosis in monocytic cells by activating ERK signaling. Journal of Lipid Research, 49(1), 58–65. https://doi.org/10.1194/jlr.M700100-JLR200
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.