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In Vivo Polarization of M2 Macrophages by Mesenchymal Stem Cell-Derived Extracellular Vesicles: A Novel Approach to Macrophage Polarization and Its Potential in Treating Inflammatory Diseases Publisher



Soufihasanabad S1 ; Mahmoudi M2, 3 ; Taghavifarahabadi M4 ; Mirsanei Z5 ; Mahmoudi Lamouki R6 ; Mirza Abdalla JK1 ; Babaei E1, 7 ; Hashemi SM5
Authors
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Authors Affiliations
  1. 1. Department of Biology, School of Natural Sciences, University of Tabriz, Tehran, Iran
  2. 2. Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
  3. 3. Immunology Research Center, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  6. 6. Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  7. 7. College of science, Cihan University, Erbil, Iraq

Source: Medical Hypotheses Published:2024


Abstract

Inflammation is a physiological process of the immune system, which, if it persists chronically, can contribute to inflammation-related diseases. Macrophages have a critical role in inflammation, as they undergo differentiation into M1 phenotype. One approach to managing inflammation related diseases involves the utilization of M2 macrophages and their transplantation into the host. However, the in vivo application of mediators that can induce M2 polarization faces limitations. In recent years, it has been acknowledged that extracellular vesicles originating from mesenchymal stem cells possess favorable biocompatibility, enabling their facile in vivo utilities. This study hypothesizes that MSC-derived EVs can induce M2 macrophages in vivo, then these macrophages will be used for mitigating inflammatory conditions in many clinical conditions. These vesicles exhibit the capability to enhance M2 polarization of macrophages, therefore, representing a potential therapeutic tool for modulating macrophage function in vivo, ensuring a safer application of manipulated macrophages in diseases associated with inflammation. © 2024 Elsevier Ltd