Fibroblasts generate topographical cues that steer cancer cell migration

Author:

Baschieri Francesco1ORCID,Illand Abigail2,Barbazan Jorge3ORCID,Zajac Olivier4,Henon Clémence5ORCID,Loew Damarys6ORCID,Dingli Florent6ORCID,Vignjevic Danijela Matic4,Lévêque-Fort Sandrine2,Montagnac Guillaume1ORCID

Affiliation:

1. Inserm U1279, Gustave Roussy Institute, Université Paris-Saclay, Villejuif, France.

2. Université Paris Saclay, CNRS, Institut des sciences moléculaires d’Orsay, UMR8214, Orsay, France.

3. Translational Medical Oncology Group (ONCOMET), Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.

4. Institut Curie, UMR144, PSL Research University, Centre Universitaire, Paris, France.

5. Inserm U981, Gustave Roussy Institute, Université Paris-Saclay, Villejuif, France.

6. Institut Curie, PSL Research University, Centre de Recherche, Laboratoire de Spectrométrie de Masse Protéomique, Paris, France.

Abstract

Fibroblasts play a fundamental role in tumor development. Among other functions, they regulate cancer cells’ migration through rearranging the extracellular matrix, secreting soluble factors, and establishing direct physical contacts with cancer cells. Here, we report that migrating fibroblasts deposit on the substrate a network of tubular structures that serves as a guidance cue for cancer cell migration. Such membranous tubular network, hereafter called tracks, is stably anchored to the substrate in a β5-integrin–dependent manner. We found that cancer cells specifically adhere to tracks by using clathrin-coated structures that pinch and engulf tracks. Tracks thus represent a spatial memory of fibroblast migration paths that is read and erased by cancer cells directionally migrating along them. We propose that fibroblast tracks represent a topography-based intercellular communication system capable of steering cancer cell migration.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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