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Updated: Mar 7, 2026

Quantitative Analysis and Characterization of Atherosclerotic Lesions in the Murine Aortic Sinus
Published on: December 7, 2013
Macrophage Apoptosis and Necrotic Core Development in Atherosclerosis: A Rapidly Advancing Field with Clinical
Leticia Gonzalez1, Bernardo Louis Trigatti1
1Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada; Thrombosis and Atherosclerosis Research Institute, McMaster University, Hamilton, Ontario, Canada.
Insights
Macrophage apoptosis and efferocytosis are key in atherosclerosis plaque development, influencing necrotic core formation and plaque stability. Understanding these processes offers new avenues for treating cardiovascular diseases.
Area of Science:
- Cardiovascular Biology
- Immunology
- Cellular Pathology
Background:
- Cardiovascular diseases are a leading global cause of death.
- Atherosclerosis, driven by macrophages, contributes significantly to ischemic heart disease.
- Macrophage apoptosis is critical for necrotic core formation in unstable atherosclerotic plaques.
Purpose of the Study:
- To review the role of macrophage apoptosis and efferocytosis in atherosclerosis.
- To emphasize their contribution to necrotic core development and plaque stabilization.
- To discuss clinical implications and novel therapeutic strategies.
Main Methods:
- Review of current literature on macrophage apoptosis and efferocytosis in atherogenesis.
- Analysis of molecular triggers, cellular mediators, and ER stress.
- Exploration of imaging and therapeutic approaches.
Main Results:
- Macrophage apoptosis contributes to the necrotic core, a hallmark of unstable plaques.
- Defective efferocytosis exacerbates atherosclerotic plaque progression.
- Novel imaging and therapeutic strategies targeting macrophages show promise.
Conclusions:
- Macrophage apoptosis and efferocytosis are central to atherosclerosis progression and plaque vulnerability.
- Targeting these pathways offers potential for improved prevention and management of atherosclerotic diseases.
- Advances in macrophage science are crucial for future cardiovascular disease therapies.
Abstract:
Cardiovascular diseases represent 1 of the main causes of death worldwide, and atherosclerosis is 1 of the major contributors leading to ischemic heart disease. Macrophages actively participate in all stages of atherosclerosis development, from plaque initiation to the transition to vulnerable plaques. Macrophage apoptosis, in particular, has been recognized as a critical step in the formation of the necrotic core, a key characteristic of unstable lesions. In this review, we discuss the role of macrophage apoptosis and clearance of apoptotic cells by efferocytosis in the development of atherosclerosis, with particular emphasis on their contribution to the development of the necrotic core and the clinical implications of this process for plaque stabilization. We consider the molecular triggers of macrophage apoptosis during atherogenesis, the role of endoplasmic reticulum (ER) stress, the roles of key cellular mediators of apoptosis and efferocytosis, and mechanisms of defective efferocytosis in the progression of atherosclerotic plaques. Finally, we discuss the important clinical implications of rapidly evolving macrophage science, such as novel approaches to imaging vulnerable atherosclerotic plaques with macrophage-sensitive positron emission tomography and magnetic resonance imaging, the role of macrophages in mediating beneficial pleiotropic actions of lipid-lowering therapies, and novel therapeutic modalities targeting ER stress, autophagy, and deficient efferocytosis. Advances in understanding the critical role of macrophages in the progression and destabilization of atherosclerosis have the potential to greatly improve the prevention and management of atherosclerotic diseases over the next decade.
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