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May 14, 2009Journal of Interferon & Cytokine Research3,954 citationsOpen Access

Monocyte Chemoattractant Protein-1 (MCP-1): An Overview

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SDSatish L. DeshmaneSKSergey G. KremlevSAShohreh Amini

Key Points

  • To provide a comprehensive overview of the molecular structure, biological mechanisms, and pathological roles of monocyte chemoattractant protein-1 (MCP-1/CCL2) and its receptor CCR2.
  • Synthesized literature on the chemokine family classification based on conserved N-terminal cysteine residues.
  • Evaluated the biological mechanisms of CCL2-mediated chemotaxis, endothelial migration, and receptor signaling.
  • CCL2 selectively regulates the migration and infiltration of monocytes and macrophages via activation of the G-protein-coupled receptor CCR2.
  • Endothelial transmigration of monocytes driven by CCL2/CCR2 is required for normal immunological surveillance and becomes markedly induced in inflammatory disease states.

Abstract

Chemokines constitute a family of chemoattractant cytokines and are subdivided into four families on the basis of the number and spacing of the conserved cysteine residues in the N-terminus of the protein. Chemokines play a major role in selectively recruiting monocytes, neutrophils, and lymphocytes, as well as in inducing chemotaxis through the activation of G-protein-coupled receptors. Monocyte chemoattractant protein-1 (MCP-1/CCL2) is one of the key chemokines that regulate migration and infiltration of monocytes/macrophages. Both CCL2 and its receptor CCR2 have been demonstrated to be induced and involved in various diseases. Migration of monocytes from the blood stream across the vascular endothelium is required for routine immunological surveillance of tissues, as well as in response to inflammation. This review will discuss these biological processes and the structure and function of CCL2.

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Cite This Study

Deshmane et al. (2009) studied this question.

synapsesocial.com/papers/69d6fc7ef174babf6cab3d5ahttps://doi.org/10.1089/jir.2008.0027
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