| Literature DB >> 33098765 |
Caroline Perner1, Cameron H Flayer1, Xueping Zhu1, Pamela A Aderhold1, Zaynah N A Dewan1, Tiphaine Voisin2, Ryan B Camire3, Ohn A Chow1, Isaac M Chiu2, Caroline L Sokol4.
Abstract
Dendritic cells (DCs) of the cDC2 lineage initiate allergic immunity and in the dermis are marked by their expression of CD301b. CD301b+ dermal DCs respond to allergens encountered in vivo, but not in vitro. This suggests that another cell in the dermis may sense allergens and relay that information to activate and induce the migration of CD301b+ DCs to the draining lymph node (dLN). Using a model of cutaneous allergen exposure, we show that allergens directly activated TRPV1+ sensory neurons leading to itch and pain behaviors. Allergen-activated sensory neurons released the neuropeptide Substance P, which stimulated proximally located CD301b+ DCs through the Mas-related G-protein coupled receptor member A1 (MRGPRA1). Substance P induced CD301b+ DC migration to the dLN where they initiated T helper-2 cell differentiation. Thus, sensory neurons act as primary sensors of allergens, linking exposure to activation of allergic-skewing DCs and the initiation of an allergic immune response.Entities:
Keywords: MRGPRA1; Substance P; TRPV1; Th2; allergy; chemotaxis; dendritic cells; sensory neurons
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Year: 2020 PMID: 33098765 PMCID: PMC7677179 DOI: 10.1016/j.immuni.2020.10.001
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745