Mammalian macrophages can adopt polarization states that, depending on the exact stimuli present in their extracellular environment, can lead to very different functions. Although these different polarization states have been shown primarily for macrophages of humans and mice, it is likely that polarized macrophages with corresponding phenotypes exist across mammals. evidence of functional conservation in macrophages from teleost fish suggests that the same, or at least comparable polarization states should also be present in teleosts. However, corresponding transcriptional profiles of marker genes have not been reported thus far. In this study we confirm that macrophages from common carp can polarize into M1-and M2 phenotypes with conserved functions and corresponding transcriptional profiles compared to mammalian macrophages. Carp M1 macrophages show increased production of nitric oxide and a transcriptional profile with increased pro-inflammatory cytokines and mediators, including il6, il12 and saa. Carp M2 macrophages show increased arginase activity and a transcriptional profile with increased anti-inflammatory mediators, including cyr61, timp2b and tgm2b. our RnA sequencing approach allowed us to list, in an unbiased manner, markers discriminating between M1 and M2 macrophages of teleost fish. We discuss the importance of our findings for the evaluation of immunostimulants for aquaculture and for the identification of gene targets to generate transgenic zebrafish for detailed studies on M1 and M2 macrophages. Above all, we discuss the striking degree of evolutionary conservation of macrophage polarization in a lower vertebrate. Depending on stimuli present in their extracellular environment, mammalian macrophages can adopt polarization states that can exert very different, sometimes opposite, functions. These opposite functional differences were initially referred to as the M1/M2 paradigm 1 , in which M1 macrophages exert pro-inflammatory activities driven by Th1 cytokines as opposed to M2 macrophages that would be driven by Th2 cytokines and be involved in anti-inflammatory responses. This paradigm is primarily based on arginine metabolism, as inflammatory M1 macrophages metabolize arginine to produce anti-microbial nitric oxide (NO) while anti-inflammatory M2 macrophages utilize the same arginine to produce proline and polyamines required for cell proliferation and tissue generation. In more recent studies, the M1/M2 paradigm has been refined to include at least nine distinct macrophage activation states 2 or define M1 and M2 macrophages at the opposite ends of an entire spectrum of activation states 2-5. Different macrophage polarization states have been studied in detail in mice and men, however it remains unclear to what extend these polarized phenotypes are conserved in non-mammalian species. Although considerable differences exist between polarized macrophages of mammals including mice and men 6-8 , their M1 and M2 macrophages display comparable core phenotypes and it is likely that polarized macroph...