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Macrophage Repolarization Using Cd44-Targeting Hyaluronic Acid–Polylactide Nanoparticles Containing Curcumin Publisher Pubmed



Farajzadeh R1, 2 ; Zarghami N1, 2 ; Seratinouri H2, 3 ; Momenijavid Z1, 2 ; Farajzadeh T4 ; Jalilzadehtabrizi S1, 2 ; Sadeghisoureh S1, 2 ; Naseri N5 ; Pilehvarsoltanahmadi Y1, 2, 3, 6
Authors
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Authors Affiliations
  1. 1. Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran
  2. 2. Stem Cell Research Center, Tabriz University of Medical Science, Tabriz, Iran
  3. 3. Stem Cell and Regenerative Medicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran
  4. 4. Department of Microbiology, Zanjan Basic Sciences and Medicine Branch, Islamic Azad University, Zanjan, Iran
  5. 5. Department of Medical Nanotechnology, School of Advanced Technologies in Medicine (SATiM), Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Australian Regenerative Medicine Institute, Monash University, Clayton, VIC, Australia

Source: Artificial Cells# Nanomedicine and Biotechnology Published:2018


Abstract

The aim of this study was to evaluate the efficiency of using a natural substance, curcumin, encapsulated in CD44-targeting hyaluronate–polylactide (HA-PLA) nanoparticles (NPs) for the modulation of macrophage polarity from the pro-inflammatory M1 to anti-inflammatory M2 phenotype. For this purpose, the characterization of the NPs was monitored using 1 HNMR, FTIR, DLS and FE-SEM. The effects of curcumin-encapsulated HA-PLA NPs on the viability of LPS/IFN-γ stimulated peritoneal macrophages were determined using MTT assay. The cellular uptake of free curcumin and nano-formulated curcumin was assessed using confocal microscopy. Also, the expression levels of iNOS-2 (M1 marker), Arg-1 (M2 marker) and also pro-inflammatory cytokines were measured by real-time PCR. Data showed that the nano-formulated curcumin with spherical shape, an average diameter of 102.5 nm and high cellular uptake was significantly less toxic to peritoneal macrophages. Furthermore, the nano-formulated curcumin effectively indicated a reduction in iNOS-2 and an increase in Arg-1 levels than free curcumin. The change in macrophage phenotype by curcumin-encapsulated HA-PLA NPs could suppress the inflammation in LPS/IFN-γ stimulated macrophages as evidenced by a major reduction in pro-inflammatory cytokines. Conclusively, the results suggested that the curcumin formulation with CD44-targeting HA-PLA NPs might be a promising platform for the treatment of inflammatory diseases. © 2017, © 2017 Informa UK Limited, trading as Taylor & Francis Group.