Abstract

Tissue infiltration of macrophages, although critical for innate immunity, is also involved in pathologies, such as chronic inflammation and cancer. In vivo, macrophages migrate mostly in a constrained three-dimensional (3D) environment. However, in vitro studies, mainly focused on two dimensions, do not provide meaningful clues about the mechanisms involved in 3D macrophage migration. In contrast, tumor cell 3D migration is well documented. It comprises a protease-independent and Rho kinase (ROCK)-dependent amoeboid migration mode and a protease-dependent and ROCK-independent mesenchymal migration mode. In this study, we examined the influence of extracellular matrix (composition, architecture, and stiffness) on 3D migration of human macrophages derived from blood monocytes (MDMs). We show that: 1) MDMs use either the amoeboid migration mode in fibrillar collagen I or the mesenchymal migration mode in Matrigel and gelled collagen I, whereas HT1080 tumor cells only perform mesenchymal migration; 2) when MDMs use the mesenchymal migratory mode, they form 3D collagenolytic structures at the tips of cell protrusions that share several markers with podosomes as described in two dimensions; 3) in contrast to tumor cells, matrix metalloproteinase inhibitors do not impair protease-dependent macrophage 3D migration, suggesting the involvement of other proteolytic systems; and 4) MDMs infiltrating matrices of similar composition but with variable stiffness adapt their migration mode primarily to the matrix architecture. In conclusion, although it is admitted that leukocytes 3D migration is restricted to the amoeboid mode, we show that human macrophages also perform the mesenchymal mode but in a distinct manner than tumor cells, and they naturally adapt their migration mode to the environmental constraints.

Highlights

  • We examined the influence of extracellular matrix on 3D migration of human macrophages derived from blood monocytes (MDMs)

  • We show that human monocyte-derived macrophages (MDMs) are able to perform either amoeboid or mesenchymal migration and choose their migratory mode according to the biophysical parameters of the matrix

  • To unravel human MDM 3D migration, we chose the 3D migration models currently used in studies with invasive tumor cells, which are acellular extracellular matrix (ECM) composed of either fibrous collagen I or Matrigel [9, 12, 34]

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Summary

Introduction

As the amoeboid migration mode of U937 macrophages has been previously described in fibrillar collagen I matrix [22], we used this matrix to study MDM 3D migration. In contrast to MDMs, in fibrillar collagen I, HT1080 tumor cells have a mesenchymal migration mode [18, 20].

Results
Conclusion
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