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Stimulation of Innate Immune Cells by Light-Activated TLR7/8 Agonists
[Image: see text] The innate immune response is controlled, in part, by the synergistic interaction of multiple Toll-like receptors (TLRs). This multi-receptor cooperation is responsible for the potent activity of many vaccines, but few tools have been developed to understand the spatio-temporal ele...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132957/ https://www.ncbi.nlm.nih.gov/pubmed/25029205 http://dx.doi.org/10.1021/ja412314j |
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author | Ryu, Keun Ah Stutts, Lalisa Tom, Janine K. Mancini, Rock J. Esser-Kahn, Aaron P. |
author_facet | Ryu, Keun Ah Stutts, Lalisa Tom, Janine K. Mancini, Rock J. Esser-Kahn, Aaron P. |
author_sort | Ryu, Keun Ah |
collection | PubMed |
description | [Image: see text] The innate immune response is controlled, in part, by the synergistic interaction of multiple Toll-like receptors (TLRs). This multi-receptor cooperation is responsible for the potent activity of many vaccines, but few tools have been developed to understand the spatio-temporal elements of TLR synergies. In this Communication, we present photo-controlled agonists of TLR7/8. By strategically protecting the active agonist moiety based on an agonist-bound crystal structure, TLR activity is suppressed and then regained upon exposure to light. We confirmed NF-κB production upon light exposure in a model macrophage cell line. Primary cell activity was confirmed by examining cytokine and cell surface marker production in bone-marrow-derived dendritic cells. Finally, we used light to activate dendritic cell sub-populations within a larger population. |
format | Online Article Text |
id | pubmed-4132957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41329572015-07-16 Stimulation of Innate Immune Cells by Light-Activated TLR7/8 Agonists Ryu, Keun Ah Stutts, Lalisa Tom, Janine K. Mancini, Rock J. Esser-Kahn, Aaron P. J Am Chem Soc [Image: see text] The innate immune response is controlled, in part, by the synergistic interaction of multiple Toll-like receptors (TLRs). This multi-receptor cooperation is responsible for the potent activity of many vaccines, but few tools have been developed to understand the spatio-temporal elements of TLR synergies. In this Communication, we present photo-controlled agonists of TLR7/8. By strategically protecting the active agonist moiety based on an agonist-bound crystal structure, TLR activity is suppressed and then regained upon exposure to light. We confirmed NF-κB production upon light exposure in a model macrophage cell line. Primary cell activity was confirmed by examining cytokine and cell surface marker production in bone-marrow-derived dendritic cells. Finally, we used light to activate dendritic cell sub-populations within a larger population. American Chemical Society 2014-07-16 2014-08-06 /pmc/articles/PMC4132957/ /pubmed/25029205 http://dx.doi.org/10.1021/ja412314j Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Ryu, Keun Ah Stutts, Lalisa Tom, Janine K. Mancini, Rock J. Esser-Kahn, Aaron P. Stimulation of Innate Immune Cells by Light-Activated TLR7/8 Agonists |
title | Stimulation
of Innate Immune Cells by Light-Activated
TLR7/8 Agonists |
title_full | Stimulation
of Innate Immune Cells by Light-Activated
TLR7/8 Agonists |
title_fullStr | Stimulation
of Innate Immune Cells by Light-Activated
TLR7/8 Agonists |
title_full_unstemmed | Stimulation
of Innate Immune Cells by Light-Activated
TLR7/8 Agonists |
title_short | Stimulation
of Innate Immune Cells by Light-Activated
TLR7/8 Agonists |
title_sort | stimulation
of innate immune cells by light-activated
tlr7/8 agonists |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132957/ https://www.ncbi.nlm.nih.gov/pubmed/25029205 http://dx.doi.org/10.1021/ja412314j |
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