| Literature DB >> 23886694 |
Ioana Madalina Fenyo1, Anca Violeta Gafencu.
Abstract
Atherosclerosis is a progressive chronic disease of large and medium arteries, characterized by the formation of atherosclerotic plaques. Monocytes and macrophages are key factors in lesion development, participating to the processes that mediate the progression of the atherosclerotic plaque (lipid accumulation, secretion of pro-inflammatory and cytotoxic factors, extracellular matrix remodeling). The recruitment of the monocytes in the vascular wall represents a hallmark in the pathology of the atherosclerotic lesion. Monocyte adhesion and transmigration are dependent on the complementary adhesion molecules expressed on the endothelial surface, whose expression is modulated by chemical mediators. The atherosclerotic plaque is characterized by a heterogeneous population of macrophages reflecting the complexity and diversity of the micro-environment to which cells are exposed after entering the arterial wall. Within the atherosclerotic lesions, macrophages differentiate, proliferate and undergo apoptosis. Taking into account that their behavior has a direct and critical influence on all lesional stages, the development of therapeutic approaches to target monocytes/macrophages in the atherosclerotic plaque became a focal interest point for researchers in the field.Entities:
Keywords: Atherosclerotic plaque; Differentiation; ECs; GM-CSF; ICAM-1; IL; Inflammation; LDL; M-CSF; MCP-1; Macrophages; Monocytes; PKC; Polarization; ROS; SMCs; TGF; TNF; VCAM-1; apoE; apolipoprotein E; endothelial cells; granulocyte/macrophage colony stimulating factor; intercellular adhesion molecule 1; interleukin; low density lipoproteins; macrophage colony stimulating factor; monocyte chemoattractant protein-1; oxLDL; oxidized LDL; protein kinase C; reactive oxygen species; smooth muscle cells; transforming growth factor; tumor necrosis factor; vascular cell adhesion molecule 1
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Year: 2013 PMID: 23886694 DOI: 10.1016/j.imbio.2013.06.005
Source DB: PubMed Journal: Immunobiology ISSN: 0171-2985 Impact factor: 3.144