Lymphatic exosomes promote dendritic cell migration along guidance cues

Author:

Brown Markus12,Johnson Louise A.3,Leone Dario A.1,Majek Peter4,Vaahtomeri Kari2ORCID,Senfter Daniel5,Bukosza Nora1,Schachner Helga1ORCID,Asfour Gabriele1,Langer Brigitte1,Hauschild Robert2ORCID,Parapatics Katja4,Hong Young-Kwon6,Bennett Keiryn L.4,Kain Renate1ORCID,Detmar Michael7ORCID,Sixt Michael2,Jackson David G.3ORCID,Kerjaschki Dontscho1ORCID

Affiliation:

1. Clinical Department of Pathology, Medical University of Vienna, Vienna, Austria

2. Institute of Science and Technology, Klosterneuburg, Austria

3. Medical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford, England, UK

4. CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria

5. Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria

6. Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA

7. Institute of Pharmaceutical Sciences, Swiss Federal Institute of Technology, ETH Zurich, Zurich, Switzerland

Abstract

Lymphatic endothelial cells (LECs) release extracellular chemokines to guide the migration of dendritic cells. In this study, we report that LECs also release basolateral exosome-rich endothelial vesicles (EEVs) that are secreted in greater numbers in the presence of inflammatory cytokines and accumulate in the perivascular stroma of small lymphatic vessels in human chronic inflammatory diseases. Proteomic analyses of EEV fractions identified >1,700 cargo proteins and revealed a dominant motility-promoting protein signature. In vitro and ex vivo EEV fractions augmented cellular protrusion formation in a CX3CL1/fractalkine-dependent fashion and enhanced the directional migratory response of human dendritic cells along guidance cues. We conclude that perilymphatic LEC exosomes enhance exploratory behavior and thus promote directional migration of CX3CR1-expressing cells in complex tissue environments.

Funder

Austrian Science Fund

Medizinische Universität Wien

European Research Council

Austrian Academy of Sciences

Medical Research Council

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Advanced European Research Council

Academy of Finland

Horizon 2020 Framework Programme

Publisher

Rockefeller University Press

Subject

Cell Biology

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