Cargando…

Environmental Allergens Trigger Type 2 Inflammation Through Ripoptosome Activation

Environmental allergens including fungi, insects and mites trigger type 2 immunity; however, the innate sensing mechanisms and initial signaling events remain unclear. Herein, we demonstrate that allergens trigger RIPK1-caspase 8 ripoptosome activation in epithelial cells. The active caspase 8 subse...

Descripción completa

Detalles Bibliográficos
Autores principales: Brusilovsky, Michael, Rochman, Mark, Rochman, Yrina, Caldwell, Julie M., Mack, Lydia E., Felton, Jennifer M., Habel, Jeff E., Porollo, Aleksey, Pasare, Chandrashekhar, Rothenberg, Marc E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487942/
https://www.ncbi.nlm.nih.gov/pubmed/34531562
http://dx.doi.org/10.1038/s41590-021-01011-2
_version_ 1784578055281311744
author Brusilovsky, Michael
Rochman, Mark
Rochman, Yrina
Caldwell, Julie M.
Mack, Lydia E.
Felton, Jennifer M.
Habel, Jeff E.
Porollo, Aleksey
Pasare, Chandrashekhar
Rothenberg, Marc E.
author_facet Brusilovsky, Michael
Rochman, Mark
Rochman, Yrina
Caldwell, Julie M.
Mack, Lydia E.
Felton, Jennifer M.
Habel, Jeff E.
Porollo, Aleksey
Pasare, Chandrashekhar
Rothenberg, Marc E.
author_sort Brusilovsky, Michael
collection PubMed
description Environmental allergens including fungi, insects and mites trigger type 2 immunity; however, the innate sensing mechanisms and initial signaling events remain unclear. Herein, we demonstrate that allergens trigger RIPK1-caspase 8 ripoptosome activation in epithelial cells. The active caspase 8 subsequently engages caspases 3 and 7, which directly mediate intracellular maturation and release of IL-33, a pro-atopy, innate immunity, alarmin cytokine. Mature IL-33 maintained functional interaction with the cognate ST2 receptor and elicited potent pro-atopy inflammatory activity in vitro and in vivo. Inhibiting caspase 8 pharmacologically and deleting murine Il33 and Casp8 each attenuated allergic inflammation in vivo. Clinical data substantiated ripoptosome activation and IL-33 maturation as likely contributors to human allergic inflammation. Our findings reveal an epithelial barrier, allergen-sensing mechanism that converges on the ripoptosome as an intracellular molecular signaling platform triggering type 2 innate immune responses. These findings have significant implications for understanding and treating human allergic diseases.
format Online
Article
Text
id pubmed-8487942
institution National Center for Biotechnology Information
language English
publishDate 2021
record_format MEDLINE/PubMed
spelling pubmed-84879422022-03-16 Environmental Allergens Trigger Type 2 Inflammation Through Ripoptosome Activation Brusilovsky, Michael Rochman, Mark Rochman, Yrina Caldwell, Julie M. Mack, Lydia E. Felton, Jennifer M. Habel, Jeff E. Porollo, Aleksey Pasare, Chandrashekhar Rothenberg, Marc E. Nat Immunol Article Environmental allergens including fungi, insects and mites trigger type 2 immunity; however, the innate sensing mechanisms and initial signaling events remain unclear. Herein, we demonstrate that allergens trigger RIPK1-caspase 8 ripoptosome activation in epithelial cells. The active caspase 8 subsequently engages caspases 3 and 7, which directly mediate intracellular maturation and release of IL-33, a pro-atopy, innate immunity, alarmin cytokine. Mature IL-33 maintained functional interaction with the cognate ST2 receptor and elicited potent pro-atopy inflammatory activity in vitro and in vivo. Inhibiting caspase 8 pharmacologically and deleting murine Il33 and Casp8 each attenuated allergic inflammation in vivo. Clinical data substantiated ripoptosome activation and IL-33 maturation as likely contributors to human allergic inflammation. Our findings reveal an epithelial barrier, allergen-sensing mechanism that converges on the ripoptosome as an intracellular molecular signaling platform triggering type 2 innate immune responses. These findings have significant implications for understanding and treating human allergic diseases. 2021-09-16 2021-10 /pmc/articles/PMC8487942/ /pubmed/34531562 http://dx.doi.org/10.1038/s41590-021-01011-2 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Brusilovsky, Michael
Rochman, Mark
Rochman, Yrina
Caldwell, Julie M.
Mack, Lydia E.
Felton, Jennifer M.
Habel, Jeff E.
Porollo, Aleksey
Pasare, Chandrashekhar
Rothenberg, Marc E.
Environmental Allergens Trigger Type 2 Inflammation Through Ripoptosome Activation
title Environmental Allergens Trigger Type 2 Inflammation Through Ripoptosome Activation
title_full Environmental Allergens Trigger Type 2 Inflammation Through Ripoptosome Activation
title_fullStr Environmental Allergens Trigger Type 2 Inflammation Through Ripoptosome Activation
title_full_unstemmed Environmental Allergens Trigger Type 2 Inflammation Through Ripoptosome Activation
title_short Environmental Allergens Trigger Type 2 Inflammation Through Ripoptosome Activation
title_sort environmental allergens trigger type 2 inflammation through ripoptosome activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487942/
https://www.ncbi.nlm.nih.gov/pubmed/34531562
http://dx.doi.org/10.1038/s41590-021-01011-2
work_keys_str_mv AT brusilovskymichael environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT rochmanmark environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT rochmanyrina environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT caldwelljuliem environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT macklydiae environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT feltonjenniferm environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT habeljeffe environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT porolloaleksey environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT pasarechandrashekhar environmentalallergenstriggertype2inflammationthroughripoptosomeactivation
AT rothenbergmarce environmentalallergenstriggertype2inflammationthroughripoptosomeactivation