SR-A (class A macrophage scavenger receptor) is a transmembrane receptor that can bind many different ligands, including modified lipoproteins that are relevant to the development of vascular diseases. However, the precise endocytic pathways of SR-A/mediated ligands internalization are not fully characterized. In this study, we show that the SR-A/ligand complex can be endocytosed by both clathrin- and caveolae-dependent pathways. Internalizations of SR-A-lipoprotein (such as acLDL) complexes primarily go through clathrin-dependent endocytosis. In contrast, macrophage apoptosis triggered by SR-A-fucoidan internalization requires caveolae-dependent endocytosis. The caveolae-dependent process activates p38 kinase and JNK signaling, whereas the clathrin-mediated endocytosis elicits ERK signaling. Our results suggest that different SR-A endocytic pathways have distinct functional consequences due to the activation of different signaling cascades in macrophages. © 2011 by The American Society for Biochemistry and Molecular Biology, Inc.
CITATION STYLE
Zhu, X. D., Zhuang, Y., Ben, J. J., Qian, L. L., Huang, H. P., Bai, H., … Chen, Q. (2011). Caveolae-dependent endocytosis is required for class a macrophage scavenger receptor-mediated apoptosis in macrophages. Journal of Biological Chemistry, 286(10), 8231–8239. https://doi.org/10.1074/jbc.M110.145888
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