Self-RNA–antimicrobial peptide complexes activate human dendritic cells through TLR7 and TLR8
The University of Texas MD Anderson Cancer Center · Melanoma Institute Australia · +3 more institutions
Abstract
Dendritic cell (DC) responses to extracellular self-DNA and self-RNA are prevented by the endosomal seclusion of nucleic acid-recognizing Toll-like receptors (TLRs). In psoriasis, however, plasmacytoid DCs (pDCs) sense self-DNA that is transported to endosomal TLR9 upon forming a complex with the antimicrobial peptide LL37. Whether LL37 also interacts with extracellular self-RNA and how this may contribute to DC activation in psoriasis is not known. Here, we report that LL37 can bind self-RNA released by dying cells, protect it from extracellular degradation, and transport it into endosomal compartments of DCs. In pDC, self-RNA-LL37 complexes activate TLR7 and, like self-DNA-LL37 complexes, trigger the…
Citation impact
- FWCI
- 17.82
- Percentile
- 100%
- References
- 44
Authors
10- DGDipyaman Ganguly
The University of Texas MD Anderson Cancer Center, Melanoma Institute Australia, Institute of Immunology
- GCGeorgios Chamilos
The University of Texas MD Anderson Cancer Center, Melanoma Institute Australia, Institute of Immunology
- RLRoberto Lande
The University of Texas MD Anderson Cancer Center, Melanoma Institute Australia, Institute of Immunology
- JGJosh Gregorio
The University of Texas MD Anderson Cancer Center, Melanoma Institute Australia, Institute of Immunology
- SMStephan Meller
The University of Texas MD Anderson Cancer Center, Melanoma Institute Australia, Institute of Immunology
Topics & keywords
- TLR7
- RNA
- Endosome
- Cell biology
- Cathelicidin
- Biology
- Innate immune system
- TLR3