Abstract

Macrophages can change their phenotype in response to environmental cues. Polarized macrophages are broadly classified into two groups: classical activated M1 and alternative activated M2. Characterization of human macrophages has been widely studied, but polarized macrophages in rabbits have not been characterized. We characterized rabbit macrophages that were polarized using human recombinant GM‐CSF and M‐CSF. GM‐CSF‐treated macrophages had higher mRNA expression of proinflammatory cytokines (M1 phenotype) than did the M‐CSF‐treated counterpart. By contrast, high levels of TGF‐β and IL‐10 expression (M2 phenotype) were found in M‐CSF‐treated macrophages. The present study may be useful to understand roles of polarized macrophages in rabbit disease models.

Highlights

  • IntroductionRabbits (the family of Leporidae) play important roles both in agriculture and as medical research animals

  • Rabbits play important roles both in agriculture and as medical research animals

  • The messenger RNA (mRNA) levels of IL-12 p35, IL-12/23 p40, IL-1b, IL-6, and tumor necrosis factor (TNF)-a genes were analyzed as M1 phenotypic markers, and IL-10 and transforming growth factor (TGF)-b were analyzed as M2 markers

Read more

Summary

Introduction

Rabbits (the family of Leporidae) play important roles both in agriculture and as medical research animals. They are widely used for basic and clinical research of human diseases because they are phylogenetically more closely related to primates than are rodents. Macrophages play a crucial role in inflammation in response to microorganisms and injuries. They have homeostatic and metabolic functions including ironcontrol, and tissue repair and remodeling [10,11]. Macrophages display remarkable plasticity and can change their physiology in response to environmental cues [12] Understanding the role of rabbit M1 and M2 macrophages in tissues is important to develop advanced procedures for diagnosis and treatment as well as new experimental models in rabbit

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call