protrusion-force-microscopy-method-to-quantify-forces-developed-cell

Protrusion Force Microscopy: A Method to Quantify Forces Developed by Cell Protrusions

In numerous biological contexts, animal cells need to interact physically with their environment by developing mechanical forces. Among these, traction ...

IPBS, Université de Toulouse, CNRS, UPS

Bone deficits are frequent in HIV-1-infected patients. We report here that osteoclasts, the cells specialized in bone resorption, are infected by HIV-1 in vivo in humanized mice and ex vivo in human joint biopsies. In vitro, infection of human osteoclasts occurs at different stages of osteoclastogenesis via cell-free viruses and, more efficiently, by transfer from infected T cells. HIV-1 infection markedly enhances adhesion and osteolytic activity of human osteoclasts by modifying the structure and function of the sealing zone, the osteoclast-specific bone degradation machinery. Indeed, the sealing zone is broader due to F-actin enrichment of its basal units (i.e., the podosomes). The viral protein Nef is involved in all HIV-1-induced effects partly through the activation of Src, a regulator of podosomes and of their assembly as a sealing zone. Supporting these results, Nef-transgenic mice exhibit an increased osteoclast density and bone defects, and osteoclasts derived from these animals display high osteolytic activity. Altogether, our study evidences osteoclasts as host cells for HIV-1 and their pathological contribution to bone disorders induced by this virus, in part via Nef.

Isabelle Maridonneau-Parini

Institut de Pharmacologie et Biologie Structurale

IPBS, Université de Toulouse, CNRS, UPS

Protrusion Force Microscopy: A Method to Quantify Forces Developed by Cell Protrusions

Isabelle Maridonneau-Parini

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Institut de Pharmacologie et Biologie Structurale

IPBS, Université de Toulouse, CNRS, UPS

Protrusion Force Microscopy: A Method to Quantify Forces Developed by Cell Protrusions

Institut de Pharmacologie et Biologie Structurale