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Commentary Open Access
Volume 3 | Issue 1 | DOI: https://doi.org/10.46439/signaling.3.076

Angiotensin-(1-7) steers macrophages to inflammation resolution

  • 1Animal Experimentation Center, Faculty of Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil
  • 2Postgraduate Program in Clinical and Toxicological Analysis, School of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Brazil
  • 3Signaling in Inflammation Laboratory, Department of Clinical and Toxicological Analysis, School of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Brazil
  • 4Department of Biochemistry and Immunology, Institute of Biological Sciences and Center for Advanced and Innovative Therapies, Federal University of Minas Gerais, Belo Horizonte, Brazil
  • #These authors contributed equally to this work: Lirlândia P. Sousa and Mauro M. Teixeira co-senior authors.
+ Affiliations - Affiliations

Corresponding Author

Simone de Araújo, simonearaujo@ufmg.br

Received Date: September 08, 2025

Accepted Date: September 19, 2025

Abstract

Angiotensin-(1-7) [Ang-(1-7)] is a biologically active peptide of the renin–angiotensin system (RAS) that counterbalances the actions of angiotensin II (Ang II), primarily through binding to the Mas receptor (MasR). This axis exerts significant immunomodulatory effects by influencing several features of leukocytes, including macrophage function, a central component in the resolution of inflammation. Macrophages contribute to tissue homeostasis by clearing apoptotic cells, releasing anti-inflammatory mediators and supporting tissue repair. Herein, we highlight the evidence supporting the role of Ang-(1-7) in guiding macrophages toward inflammation resolution. In this context, Ang-(1-7)/MasR signaling has been shown to induce several functions in macrophages, including suppression of pro-inflammatory activity, enhancement of apoptotic cells efferocytosis and bacterial phagocytosis, and promotion of macrophage polarization toward regulatory phenotypes.

Keywords

Macrophages, Mas receptor (MasR), Ang-(1-7), Inflammation resolution, Efferocytosis

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