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  • Open Access

HIV-1 Nef alters podosomes and promotes the mesenchymal migration in human macrophages

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Retrovirology201310 (Suppl 1) :P96

  • Published:


  • Dementia
  • Human Macrophage
  • Migration Ability
  • Macrophage Migration
  • Migration Capacity


Macrophages are a cell target of Human Immunodeficiency Virus-1 (HIV-1). They play a key role in AIDS pathogenesis as long-term viral reservoirs. As macrophages are able to migrate in all body tissues, they are also susceptible to participating in the systemic dissemination of viruses.


Here, we examined the migration ability of HIV-1-infected primary human macrophages. We show that HIV-1 infection modifies dramatically the migration of macrophages in 3-dimentionnal (3D) environments. While the amoeboid migration mode is inhibited upon infection, another migration mode specifically used by macrophages in dense 3D environments, the mesenchymal migration mode, is greatly enhanced. HIV-1 negative factor (Nef) is responsible for both effects on macrophage migration modes. Consistently with an increase in mesenchymal migration capacities, Nef accumulates around F-actin structures necessary for proteolysis of the extracellular matrix, e.g. podosomes, and alters their structure, function and dynamics.

Mechanistically, HIV-1-induced podosome modifications and mesenchymal macrophage migration depend on Nef’s ability to activate the macrophage-specific Src tyrosine kinase, Hck.


We conclude that HIV-1, through the action of Nef, is able to force macrophages to preferentially infiltrate some tissues. Thus, interfering with Nef/Hck interaction emerges as an unexpected strategy to reduce the spread of the virus by macrophages, for example in the brain of patients where the presence of infected macrophages is associated with neurotoxicity and AIDS-associated dementia.

Authors’ Affiliations

CNRS UMR 5089; IPBS (Institut de Pharmacologic et de Biologie Structurale), BP64182, 205 Route de Narbonne, 31077 Toulouse cedex 04, France
Université de Toulouse, UPS; IPBS, F-31077, France


© Vérollet et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.