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The aryl hydrocarbon receptor instructs the immunomodulatory profile of a subset of Clec4a4(+) eosinophils unique to the small intestine

C-type lectin domain family 4, member a4 (Clec4a4) is a C-type lectin inhibitory receptor specific for glycans thought to be exclusively expressed on murine CD8α(−) conventional dendritic cells. Using newly generated Clec4a4-mCherry knock-in mice, we identify a subset of Clec4a4-expressing eosinophi...

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Detalles Bibliográficos
Autores principales: Wang, Wei-Le, Kasamatsu, Jun, Joshita, Satoru, Gilfillan, Susan, Di Luccia, Blanda, Panda, Santosh K., Kim, Do-Hyun, Desai, Pritesh, Bando, Jennifer K., Huang, Stanley Ching-Cheng, Yomogida, Kentaro, Hoshino, Hitomi, Fukushima, Mana, Jacobsen, Elizabeth A., Van Dyken, Steven J., Ruedl, Christiane, Cella, Marina, Colonna, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9191779/
https://www.ncbi.nlm.nih.gov/pubmed/35653568
http://dx.doi.org/10.1073/pnas.2204557119
Descripción
Sumario:C-type lectin domain family 4, member a4 (Clec4a4) is a C-type lectin inhibitory receptor specific for glycans thought to be exclusively expressed on murine CD8α(−) conventional dendritic cells. Using newly generated Clec4a4-mCherry knock-in mice, we identify a subset of Clec4a4-expressing eosinophils uniquely localized in the small intestine lamina propria. Clec4a4(+) eosinophils evinced an immunomodulatory signature, whereas Clec4a4(−) eosinophils manifested a proinflammatory profile. Clec4a4(+) eosinophils expressed high levels of aryl hydrocarbon receptor (Ahr), which drove the expression of Clec4a4 as well as other immunomodulatory features, such as PD-L1. The abundance of Clec4a4(+) eosinophils was dependent on dietary AHR ligands, increased with aging, and declined in inflammatory conditions. Mice lacking AHR in eosinophils expanded innate lymphoid cells of type 2 and cleared Nippostrongylus brasiliensis infection more effectively than did wild-type mice. These results highlight the heterogeneity of eosinophils in response to tissue cues and identify a unique AHR-dependent subset of eosinophils in the small intestine with an immunomodulatory profile.