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.

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