Lymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch, National Institute of Arthritis, Musculoskeletal and Skin Diseases, NIH, Bethesda, MD 20892, USA.
Jill Roberts Institute for Research in Inflammatory Bowel Disease, Joan and Sanford I. Weill Department of Medicine, Department of Microbiology and Immunology, Weill Cornell Medicine, Cornell University, New York, NY 10021, USA.
Immunity. 2019 Oct 15;51(4):682-695.e6. doi: 10.1016/j.immuni.2019.06.009. Epub 2019 Jul 25.
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.
固有淋巴细胞维持黏膜屏障的组织稳态,其中 2 型固有淋巴样细胞(ILC2)产生 2 型细胞因子并控制寄生虫感染。虽然对 ILC2 反应的分子理解已经取得进展,但影响 ILC2 的微环境因素的复杂性变得越来越明显。在此,我们使用单细胞分析来探索寄生虫感染期间肺淋巴细胞中基因表达的多样性。感染后,我们鉴定了一组优先表达编码白细胞介素(IL)-5 的 Il5 的 ILC2,同时还表达 Calca 编码的降钙素基因相关肽(CGRP)及其同源受体成分。CGRP 与 IL-33 和神经肽 U(NMU)共同支持 IL-5,但限制了 IL-13 的表达和 ILC2 的增殖。没有 CGRP 信号,ILC2 反应和蠕虫排出增强。总之,这些数据表明 CGRP 是一种依赖于上下文的负调节因子,它在 2 型固有免疫反应期间调节警报素和神经肽对固有淋巴细胞反应的影响。