Imperial College London

ProfessorCaetanoReis e Sousa

Faculty of MedicineDepartment of Immunology and Inflammation

Visiting Professor
 
 
 
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Contact

 

c.reisesousa

 
 
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Location

 

Wright Fleming WingSt Mary's Campus

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Summary

 

Publications

Citation

BibTex format

@article{Schulz:2018:10.1016/j.celrep.2018.06.038,
author = {Schulz, O and Han, P and Böttcher, JP and Hoogeboom, R and Diebold, SS and Tolar, P and Reis, E Sousa C},
doi = {10.1016/j.celrep.2018.06.038},
journal = {Cell Reports},
pages = {419--428},
title = {Myosin II synergizes with F-actin to promote DNGR-1-dependent cross-presentation of dead cell-associated antigens},
url = {http://dx.doi.org/10.1016/j.celrep.2018.06.038},
volume = {24},
year = {2018}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Conventional type 1 DCs (cDC1s) excel at cross-presentation of dead cell-associated antigens partly because they express DNGR-1, a receptor that recognizes exposed actin filaments on dead cells. In vitro polymerized F-actin can be used as a synthetic ligand for DNGR-1. However, cellular F-actin is decorated with actin-binding proteins, which could affect DNGR-1 recognition. Here, we demonstrate that myosin II, an F-actin-associated motor protein, greatly potentiates the binding of DNGR-1 to F-actin. Latex beads coated with F-actin and myosin II are taken up by DNGR-1+ cDC1s, and antigen associated with those beads is efficiently cross-presented to CD8+ T cells. Myosin II-deficient necrotic cells are impaired in their ability to stimulate DNGR-1 or to serve as substrates for cDC1 cross-presentation to CD8+ T cells. These results provide insights into the nature of the DNGR-1 ligand and have implications for understanding immune responses to cell-associated antigens and for vaccine design.
AU - Schulz,O
AU - Han,P
AU - Böttcher,JP
AU - Hoogeboom,R
AU - Diebold,SS
AU - Tolar,P
AU - Reis,E Sousa C
DO - 10.1016/j.celrep.2018.06.038
EP - 428
PY - 2018///
SN - 2211-1247
SP - 419
TI - Myosin II synergizes with F-actin to promote DNGR-1-dependent cross-presentation of dead cell-associated antigens
T2 - Cell Reports
UR - http://dx.doi.org/10.1016/j.celrep.2018.06.038
UR - https://www.ncbi.nlm.nih.gov/pubmed/29996102
UR - http://hdl.handle.net/10044/1/61262
VL - 24
ER -