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Updated: May 11, 2026

Quantification of Monocyte Chemotactic Activity In Vivo and Characterization of Blood Monocyte Derived Macrophages
Published on: August 12, 2019
Role of monocyte chemoattractant protein-1 in myocardial infarction
Hajime Morimoto1, Masafumi Takahashi
1Department of Cardiovascular Medicine and Regeneration, Matsumoto, Japan;
Insights
Myocardial infarction (MI) involves inflammation and leukocyte recruitment. Monocyte chemoattractant protein-1 (MCP-1/CCL2) is a key chemokine in MI pathophysiology and a potential therapeutic target.
Area of Science:
- Cardiovascular Biology
- Immunology
- Molecular Medicine
Background:
- Myocardial infarction (MI) triggers inflammatory responses, including leukocyte recruitment, leading to cardiac damage, healing, and scarring.
- Chemokines, potent chemoattractant cytokines, regulate leukocyte trafficking and inflammatory processes.
- Chemokines are expressed by non-hematopoietic cells (endothelial cells, smooth muscle cells, cardiomyocytes), with functions beyond leukocyte migration.
Purpose of the Study:
- To review the critical role of chemokines, particularly monocyte chemoattractant protein-1 (MCP-1/CCL2), in the pathophysiology of myocardial infarction (MI).
- To discuss the therapeutic potential of targeting MCP-1/CCL2 in the context of MI.
Main Methods:
- Review of experimental and clinical studies investigating chemokine involvement in MI.
- Focus on the CC chemokine, monocyte chemoattractant protein-1 (MCP-1/CCL2), and its specific functions in MI.
Main Results:
- Chemokines play a significant role in the pathophysiology of MI.
- MCP-1/CCL2 is a frequently investigated chemokine implicated in MI.
Conclusions:
- MCP-1/CCL2 is integral to the pathological processes following myocardial infarction.
- Targeting MCP-1/CCL2 presents a promising therapeutic strategy for managing MI.
Abstract:
Myocardial infarction (MI) is accompanied by inflammatory responses that lead to the recruitment of leukocytes and subsequent myocardial damage, healing, and scar formation. Chemokines are a family of potent chemoattractant cytokines that regulate the leukocyte trafficking in basal levels and inflammatory processes; however, it has been recently recognized that chemokines are expressed by non-hematopoietic cells such as endothelial cells, smooth muscle cells, and cardiomyocytes, and their function extends far beyond leukocyte migration and activation. Many experimental and clinical studies have demonstrated that chemokines play an important role in the pathophysiology of MI. In particular, the CC chemokine - monocyte chemoattractant protein-1 (MCP-1/CCL2) - is one of the most frequently investigated, and it is believed to play an important role in the pathophysiology of MI. This review will focus on the role of MCP-1 in the pathophysiology of MI and discuss its potential as a therapeutic target in this condition.
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