Abstract
Conclusions: Our results indicate that TLR4 plays an important role in the process of oxLDL//2GPI/ anti-/ 2GPI complex-induced transformation of macrophages to foam cells, which may accelerate the development of atherosclerosis in the setting of APS. However,/2GPI alone functions as an anti-atherogenic protein by preventing the foam cell formation induced by oxLDL. Aim: It has been reported that oxidized low-density lipoprotein (oxLDL) forms a stable and non-dissociable complex with β2-glycoprotein I (β2GPI) and that IgG anti-/β2GPI autoantibodies are able to recognize this complex, thus facilitating macrophage-derived foam cell formation in patients with antiphospholipid syndrome (APS). However, the immunopathological mechanisms of oxLDL//hGPI complexes in promoting foam cell formation are not fully understood. In this study, we examined the role of toll-like receptor 4 (TLR4) in the oxLDL//β2GPI/anti-/β2GPI complex-induced transformation of mouse peritoneal macrophages to foam cells. Methods: Oil red O staining and optical density (OD) measurements of intracellular stained oil red O solution were used to monitor the transformation of peritoneal macrophages to foam cells in TLR4-competent C3H/HeN and TLR4-mutant C3H/HeJ mice. During foam cell formation induced by the oxLDL/ /β2GPI/anti-/?2GPI complex, the expression of TLR4 and activation of nuclear factor kappa B (NF-kB) were confirmed by analyzing the protein and mRNA levels of these compounds. Furthermore, the related active molecule expression during foam cell formation induced by the oxLDL// 2GPI/anti-/ 2GPI complex was examined in the presence or absence of TLR4. Results: The data showed that treatment with the oxLDL//β2GPI/anti-/?2GPI complex markedly increased foam cell formation, the TLR4 expression, NF-kB activation, the tissue factor (TF) expression and tumor necrosis factor-a (TNF-a) and monocyte chemotactic protein-1 (MCP-1) secretion in the C3H/HeN mice. However, the transformation of macrophages to foam cells and the expression levels of phosphorylated NF-kB, TF, TNF-a and MCP-1 were significantly reduced in the C3H/HeJ mice treated with the oxLDL// 2GPI/anti-/ 2GPI complex. In addition, compared with that achieved by oxLDL alone, the oxLDL// 2GPI complex decreased foam cell formation and the related signaling molecule expression in the C3H/HeN mice.
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Zhang, X., Xie, Y., Zhou, H., Xu, Y., Liu, J., Xie, H., & Yan, J. (2014). Involvement of TLR4 in oxidized LDL/β2GPI/Anti-β2GPI-induced transformation of macrophages to foam cells. Journal of Atherosclerosis and Thrombosis, 21(11), 1140–1151. https://doi.org/10.5551/jat.24372
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