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Saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on PERK activation

Saponin-based adjuvants (SBAs) are promising new adjuvants that stand out as they not only enforce CD4 + T cell-mediated immunity and antibody responses, but also induce an unprecedented level of antigen cross-presentation by dendritic cells (DC) and subsequent CD8 + T cell activation. We discovered...

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Autores principales: Huis in ’t Veld, Lisa G. M., Ho, Nataschja I., Wassink, Melisssa, den Brok, Martijn H., Adema, Gosse J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994093/
https://www.ncbi.nlm.nih.gov/pubmed/35396971
http://dx.doi.org/10.1007/s00018-022-04253-x
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author Huis in ’t Veld, Lisa G. M.
Ho, Nataschja I.
Wassink, Melisssa
den Brok, Martijn H.
Adema, Gosse J.
author_facet Huis in ’t Veld, Lisa G. M.
Ho, Nataschja I.
Wassink, Melisssa
den Brok, Martijn H.
Adema, Gosse J.
author_sort Huis in ’t Veld, Lisa G. M.
collection PubMed
description Saponin-based adjuvants (SBAs) are promising new adjuvants that stand out as they not only enforce CD4 + T cell-mediated immunity and antibody responses, but also induce an unprecedented level of antigen cross-presentation by dendritic cells (DC) and subsequent CD8 + T cell activation. We discovered that SBA’s ability to boost cross-presentation depends on the induction of lipid bodies (LBs). Moreover, the MHCII(lo)CD11b(hi) DC subset was identified to be most responsive to SBA-induced cross-presentation. The aim is to further unravel the mechanisms behind the induction of DC cross-presentation by SBAs. Here we show that SBAs specifically induce the PKR-like Endoplasmic Reticulum kinase (PERK) pathway and that SBA-induced DC cross-presentation is dependent on activation of the PERK pathway. PERK activation and LB formation are both crucial for SBA-induced cross-presentation and PERK inhibition has little or no effect on SBA-induced LB formation. SBA’s responsiveness, LB formation and PERK activation are specific for the MHCII(lo)CD11b(hi) DCs. These findings contribute to understanding the pathways involved in SBA-induced cross-presentation and immune activation which will ultimately lead to the development of vaccines with improved efficiency and safety. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04253-x.
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spelling pubmed-89940932022-04-11 Saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on PERK activation Huis in ’t Veld, Lisa G. M. Ho, Nataschja I. Wassink, Melisssa den Brok, Martijn H. Adema, Gosse J. Cell Mol Life Sci Original Article Saponin-based adjuvants (SBAs) are promising new adjuvants that stand out as they not only enforce CD4 + T cell-mediated immunity and antibody responses, but also induce an unprecedented level of antigen cross-presentation by dendritic cells (DC) and subsequent CD8 + T cell activation. We discovered that SBA’s ability to boost cross-presentation depends on the induction of lipid bodies (LBs). Moreover, the MHCII(lo)CD11b(hi) DC subset was identified to be most responsive to SBA-induced cross-presentation. The aim is to further unravel the mechanisms behind the induction of DC cross-presentation by SBAs. Here we show that SBAs specifically induce the PKR-like Endoplasmic Reticulum kinase (PERK) pathway and that SBA-induced DC cross-presentation is dependent on activation of the PERK pathway. PERK activation and LB formation are both crucial for SBA-induced cross-presentation and PERK inhibition has little or no effect on SBA-induced LB formation. SBA’s responsiveness, LB formation and PERK activation are specific for the MHCII(lo)CD11b(hi) DCs. These findings contribute to understanding the pathways involved in SBA-induced cross-presentation and immune activation which will ultimately lead to the development of vaccines with improved efficiency and safety. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04253-x. Springer International Publishing 2022-04-09 2022 /pmc/articles/PMC8994093/ /pubmed/35396971 http://dx.doi.org/10.1007/s00018-022-04253-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Huis in ’t Veld, Lisa G. M.
Ho, Nataschja I.
Wassink, Melisssa
den Brok, Martijn H.
Adema, Gosse J.
Saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on PERK activation
title Saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on PERK activation
title_full Saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on PERK activation
title_fullStr Saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on PERK activation
title_full_unstemmed Saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on PERK activation
title_short Saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on PERK activation
title_sort saponin-based adjuvant-induced dendritic cell cross-presentation is dependent on perk activation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994093/
https://www.ncbi.nlm.nih.gov/pubmed/35396971
http://dx.doi.org/10.1007/s00018-022-04253-x
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