Abstract

Cell-to-cell communication is essen for the development of multicellular systems and is coordinated by soluble factors, exosomes, gap junction (GJ) channels, and the recently described tunneling nanotubes (TNTs). We and others have demonstrated that TNT-like structures are mostly present during pathogenic conditions, including HIV infection. However, the nature, function, and communication properties of TNTs are still poorly understood. In this manuscript, we demonstrate that TNTs induced by HIV infection have functional GJs at the ends of their membrane extensions and that TNTs mediate long-range GJ communication during HIV infection. Blocking or reducing GJ communication during HIV infection resulted in aberrant TNT cell-to-cell contact, compromising HIV spread and replication. Thus, TNTs and associated GJs are required for the efficient cell-to-cell communication and viral spread. Our data indicate that targeting TNTs/GJs may provide new therapeutic opportunities for the treatment of HIV.

Highlights

  • In this study, we present evidence of direct physical interplay between tunneling nanotubes (TNTs) and gap junction (GJ) during HIV infection

  • We examined TNTs using scanning (SEM) and transmission (TEM) electron microscopy

  • After 60–80% of the cells were positive for HIV-p24, TNT formation or stability decreased to control levels, suggesting that TNT are only necessary during the active cell to cell infection process

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Summary

Introduction

We present evidence of direct physical interplay between TNTs and GJs during HIV infection. Higher magnification of the ends of the TNT processes indicated that the connections between HIV-infected and uninfected macrophages were mostly of the synaptic kind (Fig. 1F).

Results
Conclusion
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