Neuropeptide CGRP Limits Group 2 Innate Lymphoid Cell Responses and Constrains Type 2 Inflammation

神经肽CGRP限制2型固有淋巴细胞反应并抑制2型炎症

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作者:Hiroyuki Nagashima ,Tanel Mahlakõiv ,Han-Yu Shih ,Fred P Davis ,Francoise Meylan ,Yuefeng Huang ,Oliver J Harrison ,Chen Yao ,Yohei Mikami ,Joseph F Urban Jr ,Kathleen M Caron ,Yasmine Belkaid ,Yuka Kanno ,David Artis ,John J O'Shea

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.

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