Abstract

Macrophages play a crucial rule in orchestrating immune responses against pathogens and foreign materials. Macrophages have remarkable plasticity in response to environmental cues and are able to acquire a spectrum of activation status, best exemplified by pro-inflammatory (M1) and anti-inflammatory (M2) phenotypes at the two ends of the spectrum. Characterisation of M1 and M2 subsets is usually carried out by quantification of multiple cell surface markers, transcription factors and cytokine profiles. These approaches are time-consuming, require large numbers of cells and are resource intensive. In this study, we used machine learning algorithms to develop a simple and fast imaging-based approach that enables automated identification of different macrophage functional phenotypes using their cell size and morphology. Fluorescent microscopy was used to assess cell morphology of different cell types which were stained for nucleus and actin distribution using DAPI and phalloidin respectively. By only analysing their morphology we were able to identify M1 and M2 phenotypes effectively and could distinguish them from naïve macrophages and monocytes with an average accuracy of 90%. Thus we suggest high-content and automated image analysis can be used for fast phenotyping of functionally diverse cell populations with reasonable accuracy and without the need for using multiple markers.

Highlights

  • As a component of the innate immune system, macrophages play a central role in defence against pathogens as well as maintaining the body’s haemostasis

  • Human peripheral blood monocytes were differentiated into macrophages in vitro in the presence of GM-CSF, IFN-γ and GM-CSF (M1 macrophages) or IL-4 and macrophage colony-stimulating factor (M-CSF) (M2 macrophages) for 6 days

  • Immunofluorescent staining for the activation markers calprotectin and MR (CD206) demonstrated that M1 macrophages had the highest expression of calprotectin, while expression of this marker was much lower on M2 macrophages and naïve macrophages and not detected in untreated monocytes (Fig. 1)

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Summary

Introduction

As a component of the innate immune system, macrophages play a central role in defence against pathogens as well as maintaining the body’s haemostasis. M1 macrophages have pro-inflammatory and anti-tumour functions[4] and secrete high levels of pro-inflammatory cytokines such as interleukin 12 (IL-12) and IL-236. M1 macrophages can be identified by the production of high levels of pro-inflammatory cytokines such as IL-12, IL-236, IL-1β, IL-6 and tumour necrosis factor alpha (TNF-α)[15, 16]. These cells have been shown to express high levels of chemokine (C-C motif) receptor 7 (CCR7)[17], nitric oxide synthase 2 (NOS2)[18], calprotectin[19], and CCR220. Human M2 macrophages, on the other hand, can be identified by high levels of Kruppel-like factor 4 (Klf4) and chitinase 3-like 2 (Chi3l2 or Ykl39) gene expression and STAT6 phosphorylation[27]

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