Canine macrophages can like human macrophages be in vitro activated toward the M2a subtype relevant in allergy. (May 2018)

• Record Type: Journal Article
• Authors: Herrmann, Ina; Gotovina, Jelena; Fazekas-Singer, Judit; Fischer, Michael B.; Hufnagl, Karin; Bianchini, Rodolfo; Jensen-Jarolim, Erika
• Is Part Of: Developmental and comparative immunology. Volume 82(2018)
• Page Start: 118
• Page End: 127
• Publication Date: 2018-05
• Subjects: Allergy -- Canine -- Comparative -- DH82 -- M1 macrophage -- M2a macrophage -- Polarization; DCs dendritic cells -- FBS fetal bovine serum -- GM-CSF granulocyte macrophage stimulating-factor -- Ig immunglobulin -- IL Interleukin -- M-CSF macrophage colony-stimulating factor -- Tm melting temperature -- MDMs monocyte-derived macrophages -- NTC no template control -- PMA phorbol 12-myristate 13-acetate -- PBS phosphate buffered saline -- r recombinant -- RT room temperature; Immunology -- Periodicals; Developmental immunology -- Periodicals; 616.079
• DOI: 10.1016/j.dci.2018.01.005
• Languages: English
• ISSNs: 0145-305X

Abstract

Abstract: The M2a subtype of macrophages plays an important role in human immunoglobulin E (IgE-mediated allergies) and other Th2 type immune reactions. In contrast, very little is known about these cells in the dog. Here we describe an in vitro method to activate canine histiocytic DH82 cells and primary canine monocyte-derived macrophages (MDMs) toward the M2a macrophages using human cytokines. For a side-by-side comparison, we compared the canine cells to human MDMs, and the human monocytic cell line U937 activated towards M1 and M2a cells on the cellular and molecular level. In analogy to activated human M2a cells, canine M2a, differentiated from both DH82 and MDMs, showed an increase in CD206 surface receptor expression compared to M1. Interestingly, canine M2a, but not M1 derived from MDM, upregulated the high-affinity IgE receptor (FcεRI). Transcription levels of M2a-associated genes (IL10, CCL22, TGFβ, CD163) showed a diverse pattern between the human and dog species, whereas M1 genes (IDO1, CXCL11, IL6, TNF-α) were similarly upregulated in canine and human M1 cells (cell lines and MDMs). We suggest that our novel in vitro method will be suitable in comparative allergology studies focussing on macrophages. Highlights: By a novel in-vitro activation method now also canine macrophages can be differentiated to M2a subtype. This can be done with canine primary monocyte-derived macrophages as well as cell line DH82 histiocytotic cells. The high affinity IgE receptor FcεRI is a specific marker for canine, but not human M2a macrophages. Comparisions of canine and human macrophages rendered a catalogue of similarities and differences.