| Literature DB >> 31353223 |
Hiroyuki Nagashima1, Tanel Mahlakõiv2, Han-Yu Shih1, Fred P Davis1, Francoise Meylan1, Yuefeng Huang3, Oliver J Harrison4, Chen Yao1, Yohei Mikami1, Joseph F Urban5, Kathleen M Caron6, Yasmine Belkaid4, Yuka Kanno7, David Artis8, John J O'Shea9.
Abstract
Innate lymphocytes maintain tissue homeostasis at mucosal barriers, with group 2 innate lymphoid cells (ILC2s) producing type 2 cytokines and controlling helminth infection. While the molecular understanding of ILC2 responses has advanced, the complexity of microenvironmental factors impacting ILC2s is becoming increasingly apparent. Herein, we used single-cell analysis to explore the diversity of gene expression among lung lymphocytes during helminth infection. Following infection, we identified a subset of ILC2s that preferentially expressed Il5-encoding interleukin (IL)-5, together with Calca-encoding calcitonin gene-related peptide (CGRP) and its cognate receptor components. CGRP in concert with IL-33 and neuromedin U (NMU) supported IL-5 but constrained IL-13 expression and ILC2 proliferation. Without CGRP signaling, ILC2 responses and worm expulsion were enhanced. Collectively, these data point to CGRP as a context-dependent negative regulatory factor that shapes innate lymphocyte responses to alarmins and neuropeptides during type 2 innate immune responses. Published by Elsevier Inc.Entities:
Keywords: CGRP; IL-33; NMU; Nippostrongylus brasiliensis; cytokines; host defense; immunoregulation; innate lymphoid cells; neuropeptides; single-cell RNA-seq
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Year: 2019 PMID: 31353223 PMCID: PMC6801073 DOI: 10.1016/j.immuni.2019.06.009
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745