Literature DB >> 30115528

Foam cell formation: A new target for fighting atherosclerosis and cardiovascular disease.

Eithne M Maguire1, Stuart W A Pearce1, Qingzhong Xiao2.   

Abstract

During atherosclerosis, the gradual accumulation of lipids into the subendothelial space of damaged arteries results in several lipid modification processes followed by macrophage uptake in the arterial wall. The way in which these modified lipoproteins are dealt with determines the likelihood of cholesterol accumulation within the monocyte-derived macrophage and thus its transformation into the foam cell that makes up the characteristic fatty streak observed in the early stages of atherosclerosis. The unique expression of chemokine receptors and cellular adhesion molecules expressed on the cell surface of monocytes points to a particular extravasation route that they can take to gain entry into atherosclerotic site, in order to undergo differentiation into the phagocytic macrophage. Indeed several GWAS and animal studies have identified key genes and proteins required for monocyte recruitment as well cholesterol handling involving lipid uptake, cholesterol esterification and cholesterol efflux. A re-examination of the previously accepted paradigm of macrophage foam cell origin has been called into question by recent studies demonstrating shared expression of scavenger receptors, cholesterol transporters and pro-inflammatory cytokine release by alternative cell types present in the neointima, namely; endothelial cells, vascular smooth muscle cells and stem/progenitor cells. Thus, therapeutic targets aimed at a more heterogeneous foam cell population with shared functions, such as enhanced protease activity, and signalling pathways, mediated by non-coding RNA molecules, may provide greater therapeutic outcome in patients. Finally, studies targeting each aspect of foam cell formation and death using both genetic knock down and pharmacological inhibition have provided researchers with a clearer understanding of the cellular processes at play, as well as helped researchers to identify key molecular targets, which may hold significant therapeutic potential in the future.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Atherosclerosis; Cardiovascular disease; Endothelial cells; Foam cell; Genetic animal model; Genome wide association studies; Macrophages; Non-coding RNAs; Pharmacological inhibition; Protease; Stem/progenitor cells; Vascular smooth muscle cells

Mesh:

Substances:

Year:  2018        PMID: 30115528     DOI: 10.1016/j.vph.2018.08.002

Source DB:  PubMed          Journal:  Vascul Pharmacol        ISSN: 1537-1891            Impact factor:   5.773


  63 in total

1.  Regulation of Macrophage Foam Cell Formation During Nitrogen Mustard (NM)-Induced Pulmonary Fibrosis by Lung Lipids.

Authors:  Alessandro Venosa; Ley Cody Smith; Alexa Murray; Tanvi Banota; Andrew J Gow; Jeffrey D Laskin; Debra L Laskin
Journal:  Toxicol Sci       Date:  2019-12-01       Impact factor: 4.849

Review 2.  Foam Cells: One Size Doesn't Fit All.

Authors:  Valentina Guerrini; Maria Laura Gennaro
Journal:  Trends Immunol       Date:  2019-11-12       Impact factor: 16.687

Review 3.  The role of smooth muscle cells in plaque stability: Therapeutic targeting potential.

Authors:  Jennifer L Harman; Helle F Jørgensen
Journal:  Br J Pharmacol       Date:  2019-08-09       Impact factor: 8.739

4.  Functions of Monocytes and Macrophages and the Associated Effective Molecules and Mechanisms at the Early Stage of Atherosclerosis.

Authors:  Liyuan Jin; Zihui Deng; Yongyi Bai; Ping Ye
Journal:  Acta Cardiol Sin       Date:  2021-09       Impact factor: 2.672

5.  Profile of IL-6 and TNF in Foam Cell Formation: An Improved Method Using Fluorescein Isothiocyanate (FITC) Probe.

Authors:  Cynthia Aparecida Castro; Tereza Cristina Buzinari; Rafael Luis Bressani Lino; Heloisa Sobreiro Selistre de Araújo; Fernanda de Freitas Aníbal; Roberto Mario Machado Verzola; Vanderlei Salvador Bagnato; Natalia Mayumi Inada; Gerson Jhonatan Rodrigues
Journal:  Arq Bras Cardiol       Date:  2022-08-05       Impact factor: 2.667

Review 6.  NLRP3 Inflammasome in Atherosclerosis: Putting Out the Fire of Inflammation.

Authors:  Bo-Zong Shao; Hai-Yan Xu; Yi-Cheng Zhao; Xiao-Rui Zheng; Fang Wang; Guan-Ren Zhao
Journal:  Inflammation       Date:  2022-08-11       Impact factor: 4.657

7.  Rutin Inhibits Ox-LDL-Mediated Macrophage Inflammation and Foam Cell Formation by Inducing Autophagy and Modulating PI3K/ATK Signaling.

Authors:  Ben Li; Yumeng Ji; Chenlong Yi; Xufeng Wang; Chaoyang Liu; Chufan Wang; Xiaohu Lu; Xiaohan Xu; Xiaowei Wang
Journal:  Molecules       Date:  2022-06-29       Impact factor: 4.927

Review 8.  Vascular smooth muscle cells in atherosclerosis: time for a re-assessment.

Authors:  Mandy O J Grootaert; Martin R Bennett
Journal:  Cardiovasc Res       Date:  2021-09-28       Impact factor: 10.787

9.  Different Effects of Endothelial Extracellular Vesicles and LPS-Induced Endothelial Extracellular Vesicles on Vascular Smooth Muscle Cells: Role of Curcumin and Its Derivatives.

Authors:  Debiao Xiang; Yamei Li; Yuling Cao; Ying Huang; Lili Zhou; Xiulian Lin; Yong Qiao; Xin Li; Duanfang Liao
Journal:  Front Cardiovasc Med       Date:  2021-05-31

10.  Propofol Ameliorates ox-LDL-Induced Endothelial Damage Through Enhancing Autophagy via PI3K/Akt/m-TOR Pathway: A Novel Therapeutic Strategy in Atherosclerosis.

Authors:  Hongyi Zhou; Fan Jiang; Yufang Leng
Journal:  Front Mol Biosci       Date:  2021-06-25
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