Irisin modulates bone marrow derived macrophage polarization towards M2 profile in high fat fed mice

Irisina modula a polarização de macrófagos derivados de medula óssea para perfil M2 em camundongos submetidos à dieta hiperlipídica

Autores

  • Juliana Magalhães-Santos
  • Rafael Loureiro Simões
  • Carla Ade Caldas
  • Silvio Rodrigues Marques-Neto
  • Thereza Christina Barja-Fidalgo
  • Eliete Bouskela
  • Raquel Carvalho Castiglione Universidade do Estado do Rio de Janeiro

DOI:

https://doi.org/10.53660/CLM-2386-23S13

Palavras-chave:

Obesity, Irisin, Macrophage

Resumo

Background and Aims: The chronic inflammatory process in the adipose tissue during obesity suggests constant polarization of classically activated macrophages (M1) and low polarization of alternately activated ones (M2). Since irisin has anti-inflammatory and antidiabetogenic properties our aim is to evaluate its effects on macrophage polarization in mice subjected to high fat diet. Methods and Results: C57Bl/6 mice were fed a high fat diet for 30 weeks. Bone marrow derived macrophages (BMDM) were isolated and incubated with 50 nM of irisin. Cellular phenotype, nitrite production, arginase-1 expression and cell viability were analyzed. Irisin was able to increase F480+CD206+ and F480+CD301+ cell number, and arginase1 expression. Irisin was not able to induce nitrite production and did not affect cell viability. Conclusion: Irisin was able to elicit an M2-like profile in macrophages in mice subjected to high fat diet, suggesting an anti-inflammatory action of this cytokine with potential therapeutic use in the control of imflammation during obesity.

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Publicado

2023-11-27

Como Citar

Magalhães-Santos, J. ., Simões, R. L. ., Caldas , C. A. ., Marques-Neto, S. R. ., Barja-Fidalgo, T. C. ., Bouskela, E., & Castiglione, R. C. . (2023). Irisin modulates bone marrow derived macrophage polarization towards M2 profile in high fat fed mice: Irisina modula a polarização de macrófagos derivados de medula óssea para perfil M2 em camundongos submetidos à dieta hiperlipídica. Concilium, 23(21), 36–50. https://doi.org/10.53660/CLM-2386-23S13

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