Abstract:
Macrophages can reversibly polarize into multiple functional subsets depending on their
micro-environment. Identification and understanding the functionality of these subsets is relevant
for the study of immune-related diseases. However, knowledge about canine macrophage
polarization is still in its infancy. In this study, we polarized canine monocytes using
GM-CSF/IFN- γ and LPS towards M1 macrophages or M-CSF and IL-4 towards M2 macrophages
and compared them to undifferentiated monocytes (M0). Polarized M1 and M2 macrophages
were thoroughly characterized for morphology, surface marker features, gene
profiles and functional properties. Our results showed that canine M1-polarized macrophages
obtained a characteristic large, roundish, or amoeboid shape, while M2-polarized
macrophages were smaller and adopted an elongated spindle-like morphology. Phenotypically,
all macrophage subsets expressed the pan-macrophage markers CD14 and CD11b.
M1-polarized macrophages expressed increased levels of CD40, CD80 CD86 and MHC II,
while a significant increase in the expression levels of CD206, CD209, and CD163 was
observed in M2-polarized macrophages. RNAseq of the three macrophage subsets showed
distinct gene expression profiles, which are closely associated with immune responsiveness,
cell differentiation and phagocytosis. However, the complexity of the gene expression
patterns makes it difficult to assign clear new polarization markers. Functionally, undifferentiated
-monocytes, and M1- and M2- like subsets of canine macrophages can all phagocytose
latex beads. M2-polarized macrophages exhibited the strongest phagocytic capacity
compared to undifferentiated monocytes- and M1-polarized cells. Taken together, this study
showed that canine M1 and M2-like macrophages have distinct features largely in parallel to those of well-studied species, such as human, mouse and pig. These findings enable future
use of monocyte derived polarized macrophages particularly in studies of immune related
diseases in dogs.
Description:
DATA AVAILABILITY STATEMENT : All relevant data are
within the manuscript and its Supporting
Information files.
SUPPORTING INFPRMATION : TABLE S1. Gene counts of M0 monocytes and M1, M2 macrophages and CD14+ and CD14D cells. TABLE S2. Differentially expressed genes of M0 monocytes, M1, M2 macrophages and CD14+ and CD14D cells. TABLE S3. Top 50 DEG pairwise comparisons M0, M1, M2 and CD14+ cells. FIGURE S1. Identification of non-viable cells by back gating. FIGURE S2. Selection of Immunity-related DEG’s. VIDE0 S1. A. Bead uptake M0 monocytes visualized by confocal microscopy. B. Bead uptake M1 MDMs visualized by confocal microscopy. C. Bead uptake M2 MDMs visualized by confocal microscopy.