Vulnerable plaque and vulnerable blood: Two critical factors for spontaneous atherothrombosis in mouse models

• Published in: Atherosclerosis 2019-05, Vol.284, p.160-164
• Main Authors: Ouweneel, Amber B., Verwilligen, Robin A.F., Van Eck, Miranda
• Format: Article
• Language: English
• Subjects: Atherothrombosis; Coagulation; Mouse models; Plaque erosion; Plaque rupture
• ISSN: 0021-9150; 1879-1484
• DOI: 10.1016/j.atherosclerosis.2019.03.006

Atherothrombotic events such as myocardial infarction and ischemic stroke are a major cause of morbidity and mortality worldwide. Understanding the molecular and cellular mechanisms of atherosclerotic plaque destabilization or erosion, and developing new therapeutics to prevent acute cardiovascular events is important for vascular biology research and clinical cardiovascular medicine. However, basic research on plaque destabilization, rupture and erosion is hampered by the lack of appropriate animal models of atherothrombosis. Unprovoked atherothrombosis is very scarce in commonly used mouse models for atherosclerosis, the low-density lipoprotein receptor knockout and apolipoprotein E knockout mice. Therefore, specific interventions are required to induce atherothrombosis in these models. Two strategies can be employed to induce atherothrombosis: 1) plaque destabilization and 2) induction of blood hypercoagulability. Although the individual strategies yield atherothrombosis at low incidence, it appears that the combination of both plaque destabilization and an increase in blood coagulability is the most promising strategy to induce atherothrombosis on a larger scale. In this review, we summarize the recent developments on mouse models for the investigation of atherothrombosis. •Preclinical atherothrombosis research is hampered by a lack of mouse models.•A combined approach is a promising strategy to induce atherothrombosis in mice.•Caution is warranted in the interpretation of plaque vulnerability in mice.