Neuromedin-U Mediates Rapid Activation of Airway Group 2 Innate Lymphoid Cells in Mild Asthma
In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate rapid host responses at mucosal interfaces. In murine models of asthma, lung ILC2s colocalize to sensory neuronal termini expressing the neuropeptide neurom...
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Published in | American journal of respiratory and critical care medicine Vol. 210; no. 6; pp. 755 - 765 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
American Thoracic Society
15.09.2024
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Abstract | In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate rapid host responses at mucosal interfaces. In murine models of asthma, lung ILC2s colocalize to sensory neuronal termini expressing the neuropeptide neuromedin U (NMU), which stimulates type 2 (T2) cytokine secretion by ILC2s, with additive effects to alarmins
.
To investigate the effect of the NMU/NMUR1 (NMU receptor 1) axis on early activation of ILC2s in asthma.
Subjects with mild asthma (
= 8) were enrolled in a diluent-controlled allergen inhalation challenge study. Sputum ILC2 expression of NMUR1 and T2 cytokines was enumerated by flow cytometry, and airway NMU levels were assessed by ELISA. This was compared with samples from subjects with moderate to severe asthma (
= 9). Flow sort-purified and
-expanded ILC2s were used for functional assays and transcriptomic analyses.
Significant increases in sputum ILC2s expressing NMUR1 were detected 7 hours after allergen versus diluent challenge whereby the majority of NMUR1
ILC2s expressed IL-5/IL-13. Sputum NMUR1
ILC2 counts were significantly greater in mild versus moderate to severe asthma, and NMUR1
ILC2s correlated inversely with the dose of inhaled corticosteroid in the latter group. Coculturing with alarmins upregulated
in ILC2s, which was attenuated by dexamethasone. NMU-stimulated T2 cytokine expression by ILC2s, maximal at 6 hours, was abrogated by dexamethasone or specific signaling inhibitors for mitogen-activated protein kinase 1/2 and phosphoinositol 3-kinase but not the IL-33 signaling moiety MyD88
.
The NMU/NMUR1 axis stimulates rapid effects on ILC2s and may be an important early activator of these cells in eosinophilic inflammatory responses in asthma. |
---|---|
AbstractList | Rationale: In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate rapid host responses at mucosal interfaces. In murine models of asthma, lung ILC2s colocalize to sensory neuronal termini expressing the neuropeptide neuromedin U (NMU), which stimulates type 2 (T2) cytokine secretion by ILC2s, with additive effects to alarmins in vitro. Objectives: To investigate the effect of the NMU/NMUR1 (NMU receptor 1) axis on early activation of ILC2s in asthma. Methods: Subjects with mild asthma (n = 8) were enrolled in a diluent-controlled allergen inhalation challenge study. Sputum ILC2 expression of NMUR1 and T2 cytokines was enumerated by flow cytometry, and airway NMU levels were assessed by ELISA. This was compared with samples from subjects with moderate to severe asthma (n = 9). Flow sort-purified and ex vivo-expanded ILC2s were used for functional assays and transcriptomic analyses. Measurements and Main Results: Significant increases in sputum ILC2s expressing NMUR1 were detected 7 hours after allergen versus diluent challenge whereby the majority of NMUR1+ ILC2s expressed IL-5/IL-13. Sputum NMUR1+ ILC2 counts were significantly greater in mild versus moderate to severe asthma, and NMUR1+ ILC2s correlated inversely with the dose of inhaled corticosteroid in the latter group. Coculturing with alarmins upregulated NMUR1 in ILC2s, which was attenuated by dexamethasone. NMU-stimulated T2 cytokine expression by ILC2s, maximal at 6 hours, was abrogated by dexamethasone or specific signaling inhibitors for mitogen-activated protein kinase 1/2 and phosphoinositol 3-kinase but not the IL-33 signaling moiety MyD88 in vitro. Conclusions: The NMU/NMUR1 axis stimulates rapid effects on ILC2s and may be an important early activator of these cells in eosinophilic inflammatory responses in asthma.Rationale: In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate rapid host responses at mucosal interfaces. In murine models of asthma, lung ILC2s colocalize to sensory neuronal termini expressing the neuropeptide neuromedin U (NMU), which stimulates type 2 (T2) cytokine secretion by ILC2s, with additive effects to alarmins in vitro. Objectives: To investigate the effect of the NMU/NMUR1 (NMU receptor 1) axis on early activation of ILC2s in asthma. Methods: Subjects with mild asthma (n = 8) were enrolled in a diluent-controlled allergen inhalation challenge study. Sputum ILC2 expression of NMUR1 and T2 cytokines was enumerated by flow cytometry, and airway NMU levels were assessed by ELISA. This was compared with samples from subjects with moderate to severe asthma (n = 9). Flow sort-purified and ex vivo-expanded ILC2s were used for functional assays and transcriptomic analyses. Measurements and Main Results: Significant increases in sputum ILC2s expressing NMUR1 were detected 7 hours after allergen versus diluent challenge whereby the majority of NMUR1+ ILC2s expressed IL-5/IL-13. Sputum NMUR1+ ILC2 counts were significantly greater in mild versus moderate to severe asthma, and NMUR1+ ILC2s correlated inversely with the dose of inhaled corticosteroid in the latter group. Coculturing with alarmins upregulated NMUR1 in ILC2s, which was attenuated by dexamethasone. NMU-stimulated T2 cytokine expression by ILC2s, maximal at 6 hours, was abrogated by dexamethasone or specific signaling inhibitors for mitogen-activated protein kinase 1/2 and phosphoinositol 3-kinase but not the IL-33 signaling moiety MyD88 in vitro. Conclusions: The NMU/NMUR1 axis stimulates rapid effects on ILC2s and may be an important early activator of these cells in eosinophilic inflammatory responses in asthma. In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate rapid host responses at mucosal interfaces. In murine models of asthma, lung ILC2s colocalize to sensory neuronal termini expressing the neuropeptide neuromedin U (NMU), which stimulates type 2 (T2) cytokine secretion by ILC2s, with additive effects to alarmins . To investigate the effect of the NMU/NMUR1 (NMU receptor 1) axis on early activation of ILC2s in asthma. Subjects with mild asthma ( = 8) were enrolled in a diluent-controlled allergen inhalation challenge study. Sputum ILC2 expression of NMUR1 and T2 cytokines was enumerated by flow cytometry, and airway NMU levels were assessed by ELISA. This was compared with samples from subjects with moderate to severe asthma ( = 9). Flow sort-purified and -expanded ILC2s were used for functional assays and transcriptomic analyses. Significant increases in sputum ILC2s expressing NMUR1 were detected 7 hours after allergen versus diluent challenge whereby the majority of NMUR1 ILC2s expressed IL-5/IL-13. Sputum NMUR1 ILC2 counts were significantly greater in mild versus moderate to severe asthma, and NMUR1 ILC2s correlated inversely with the dose of inhaled corticosteroid in the latter group. Coculturing with alarmins upregulated in ILC2s, which was attenuated by dexamethasone. NMU-stimulated T2 cytokine expression by ILC2s, maximal at 6 hours, was abrogated by dexamethasone or specific signaling inhibitors for mitogen-activated protein kinase 1/2 and phosphoinositol 3-kinase but not the IL-33 signaling moiety MyD88 . The NMU/NMUR1 axis stimulates rapid effects on ILC2s and may be an important early activator of these cells in eosinophilic inflammatory responses in asthma. Rationale: In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate rapid host responses at mucosal interfaces. In murine models of asthma, lung ILC2s colocalize to sensory neuronal termini expressing the neuropeptide neuromedin U (NMU), which stimulates type 2 (T2) cytokine secretion by ILC2s, with additive effects to alarmins in vitro. Objectives: To investigate the effect of the NMU/NMUR1 (NMU receptor 1) axis on early activation of ILC2s in asthma. Methods: Subjects with mild asthma (n = 8) were enrolled in a diluent-controlled allergen inhalation challenge study. Sputum ILC2 expression of NMUR1 and T2 cytokines was enumerated by flow cytometry, and airway NMU levels were assessed by ELISA. This was compared with samples from subjects with moderate to severe asthma (n = 9). Flow sort-purified and ex vivo-expanded ILC2s were used for functional assays and transcriptomic analyses. Measurements and Main Results: Significant increases in sputum ILC2s expressing NMUR1 were detected 7 hours after allergen versus diluent challenge whereby the majority of NMUR1+ ILC2s expressed IL-5/IL-13. Sputum NMUR1+ ILC2 counts were significantly greater in mild versus moderate to severe asthma, and NMUR1+ ILC2s correlated inversely with the dose of inhaled corticosteroid in the latter group. Coculturing with alarmins upregulated NMUR1 in ILC2s, which was attenuated by dexamethasone. NMU-stimulated T2 cytokine expression by ILC2s, maximal at 6 hours, was abrogated by dexamethasone or specific signaling inhibitors for mitogen-activated protein kinase 1/2 and phosphoinositol 3-kinase but not the IL-33 signaling moiety MyD88 in vitro. Conclusions: The NMU/NMUR1 axis stimulates rapid effects on ILC2s and may be an important early activator of these cells in eosinophilic inflammatory responses in asthma. |
Author | Ditta, Reina Gauvreau, Gail M. Howie, Karen Dvorkin-Gheva, Anna Whetstone, Christiane Wattie, Jennifer Nagashima, Akimichi Ranjbar, Maral Cusack, Ruth Sehmi, Roma O’Byrne, Paul M. Paré, Guillaume Satia, Imran Ju, Xiaotian |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38598774$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_bbcan_2025_189269 crossref_primary_10_3389_fimmu_2024_1430760 crossref_primary_10_1016_j_alit_2025_02_001 crossref_primary_10_1016_j_coi_2024_102501 crossref_primary_10_1097_ACI_0000000000001048 crossref_primary_10_1164_rccm_202404_0844ED crossref_primary_10_1016_j_coi_2024_102507 crossref_primary_10_1126_scitranslmed_ado6649 |
Cites_doi | 10.1016/j.jaci.2019.01.027 10.1038/s41590-019-0423-0 10.1126/scitranslmed.aar8477 10.3389/fimmu.2023.1130933 10.1111/imm.13257 10.1038/nature12526 10.4049/jimmunol.1300974 10.1038/nature23469 10.1164/rccm.201609-1846OC 10.1183/13993003.02135-2016 10.1038/s41467-019-09883-7 10.1126/science.aan8546 10.1210/en.2010-1463 10.1038/ni.2131 10.1038/s41586-022-05395-5 10.1183/20734735.008914 10.1164/rccm.201612-2427OC 10.1038/ni.2104 10.1164/rccm.201212-2227OC 10.1038/s41385-022-00543-6 10.1111/all.14835 10.1038/nature23676 10.1111/cea.12880 10.1165/rcmb.2022-0123OC 10.1038/nature24029 10.1046/j.1365-2222.1999.00462.x 10.1183/13993003.00536-2015 10.1111/j.1398-9995.2004.00612.x 10.1038/nri.2017.86 10.1373/clinchem.2014.231753 10.1378/chest.123.3_suppl.411S 10.1016/j.jaci.2011.08.031 10.1016/j.jaci.2015.05.037 10.1016/j.jacig.2022.07.007 10.1093/intimm/dxx040 10.1164/ajrccm.154.2.8756799 10.1016/j.immuni.2014.06.016 10.1016/j.jaci.2013.08.023 10.1038/ni.3049 10.1016/j.alit.2022.03.002 10.1159/000107052 10.1164/rccm.201909-1722OC 10.1124/pr.56.2.3 |
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References | Sehmi R (bib30) 2022; 205 bib14 bib36 bib15 bib37 bib12 bib34 bib13 bib35 bib10 bib32 bib11 bib33 bib29 bib27 bib28 bib40 bib25 bib26 bib45 bib24 bib46 bib21 bib43 bib22 Cockcroft DW (bib31) 1987; 135 bib44 bib41 bib20 bib42 bib9 bib7 bib8 bib5 bib18 bib6 bib19 bib3 bib16 bib38 bib4 bib17 bib39 bib1 bib2 Ren X (bib23) 2020; 19 38820208 - Am J Respir Crit Care Med. 2024 Sep 15;210(6):701-703. doi: 10.1164/rccm.202404-0844ED |
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Snippet | In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate rapid host... Rationale: In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate... Rationale: In asthma, sputum group 2 innate lymphoid cells (ILC2s) are activated within 7 hours after allergen challenge. Neuroimmune interactions mediate... |
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SubjectTerms | Adult Airway management Asthma Asthma - immunology Cells Cytokines Cytokines - immunology Cytokines - metabolism Female Humans Immunity, Innate Lymphocytes - immunology Lymphocytes - metabolism Male Middle Aged Neuropeptides - metabolism Receptors, Neurotransmitter Sputum - immunology |
Title | Neuromedin-U Mediates Rapid Activation of Airway Group 2 Innate Lymphoid Cells in Mild Asthma |
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