Neuro-immune Interactions Drive Tissue Programming in Intestinal Macrophages

Proper adaptation to environmental perturbations is essential for tissue homeostasis. In the intestine, diverse environmental cues can be sensed by immune cells, which must balance resistance to microorganisms with tolerance, avoiding excess tissue damage. By applying imaging and transcriptional profiling tools, we interrogated how distinct microenvironments in the gut regulate resident macrophages. We discovered that macrophages exhibit a high degree of gene-expression specialization dependent on their proximity to the gut lumen. Lamina propria macrophages (LpMs) preferentially expressed a pro-inflammatory phenotype when compared to muscularis macrophages (MMs), which displayed a tissue-protective phenotype. Upon luminal bacterial infection, MMs further enhanced tissue-protective programs, and this was attributed to swift activation of extrinsic sympathetic neurons innervating the gut muscularis and norepinephrine signaling to β2 adrenergic receptors on MMs. Our results reveal unique intra-tissue macrophage specialization and identify neuro-immune communication between enteric neurons and macrophages that induces rapid tissue-protective responses to distal perturbations.

[1]  Werner Müller,et al.  Intestinal tolerance requires gut homing and expansion of FoxP3+ regulatory T cells in the lamina propria. , 2011, Immunity.

[2]  Amin R. Mazloom,et al.  Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages , 2012, Nature Immunology.

[3]  Hongkui Zeng,et al.  A Cre-Dependent GCaMP3 Reporter Mouse for Neuronal Imaging In Vivo , 2012, The Journal of Neuroscience.

[4]  R. Locksley,et al.  Interleukin-4- and interleukin-13-mediated alternatively activated macrophages: roles in homeostasis and disease. , 2013, Annual review of immunology.

[5]  I. Amit,et al.  Tissue-Resident Macrophage Enhancer Landscapes Are Shaped by the Local Microenvironment , 2014, Cell.

[6]  N. Calakos,et al.  Neuroepithelial circuit formed by innervation of sensory enteroendocrine cells. , 2015, The Journal of clinical investigation.

[7]  M. Pellegrino,et al.  The Epithelial Cell-Derived Atopic Dermatitis Cytokine TSLP Activates Neurons to Induce Itch , 2013, Cell.

[8]  R. Locksley,et al.  Alternatively activated macrophages produce catecholamines to sustain adaptive thermogenesis , 2011, Nature.

[9]  W. Mellado,et al.  Arginase I and Polyamines Act Downstream from Cyclic AMP in Overcoming Inhibition of Axonal Growth MAG and Myelin In Vitro , 2002, Neuron.

[10]  K. Tracey Reflex control of immunity , 2009, Nature Reviews Immunology.

[11]  M. Merad,et al.  Crosstalk between Muscularis Macrophages and Enteric Neurons Regulates Gastrointestinal Motility , 2014, Cell.

[12]  M. Soares,et al.  Tissue damage control in disease tolerance. , 2014, Trends in immunology.

[13]  Kazuhiro Suzuki,et al.  Control of lymphocyte egress from lymph nodes through β2-adrenergic receptors , 2014, The Journal of experimental medicine.

[14]  D. Littman,et al.  Microbiota Restrict Trafficking of Bacteria to Mesenteric Lymph Nodes by CX3CR1hi Cells , 2013, Nature.

[15]  A. McMahon,et al.  Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase , 1998, Current Biology.

[16]  S. Srinivasan,et al.  Gut microbial products regulate murine gastrointestinal motility via Toll-like receptor 4 signaling. , 2012, Gastroenterology.

[17]  J. Bienenstock,et al.  The gut microbiome restores intrinsic and extrinsic nerve function in germ‐free mice accompanied by changes in calbindin , 2015, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

[18]  Giuseppe Penna,et al.  Oral tolerance can be established via gap junction transfer of fed antigens from CX3CR1⁺ macrophages to CD103⁺ dendritic cells. , 2014, Immunity.

[19]  F. Ginhoux,et al.  Tissue-resident macrophages self-maintain locally throughout adult life with minimal contribution from circulating monocytes. , 2013, Immunity.

[20]  Staci A. Sorensen,et al.  Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation , 2014, Front. Neural Circuits.

[21]  R. Medzhitov,et al.  Tissue-Specific Signals Control Reversible Program of Localization and Functional Polarization of Macrophages , 2014, Cell.

[22]  C. Geula,et al.  Ccr2 deficiency impairs microglial accumulation and accelerates progression of Alzheimer-like disease , 2007, Nature Medicine.

[23]  Francie Barron,et al.  Downregulation of Dlx5 and Dlx6 expression by Hand2 is essential for initiation of tongue morphogenesis , 2011, Development.

[24]  Samuel I. Miller,et al.  Identification of a Putative Salmonella enterica Serotype Typhimurium Host Range Factor with Homology to IpaH and YopM by Signature-Tagged Mutagenesis , 1999, Infection and Immunity.

[25]  R. Palmiter,et al.  Cell-type-specific isolation of ribosome-associated mRNA from complex tissues , 2009, Proceedings of the National Academy of Sciences.

[26]  J. Yates,et al.  Microglia Promote Learning-Dependent Synapse Formation through Brain-Derived Neurotrophic Factor , 2013, Cell.

[27]  J. Tack,et al.  REVIEWS IN BASIC AND CLINICAL GASTROENTEROLOGY The Serotonin Signaling System: From Basic Understanding To Drug Development for Functional GI Disorders , 2007 .

[28]  R. Ratan,et al.  Arginase 1 Regulation of Nitric Oxide Production Is Key to Survival of Trophic Factor-Deprived Motor Neurons , 2006, The Journal of Neuroscience.

[29]  Jessica Kilham,et al.  Crohn's and Colitis Foundation of America , 2014 .

[30]  Lars Råberg,et al.  Disentangling Genetic Variation for Resistance and Tolerance to Infectious Diseases in Animals , 2007, Science.

[31]  D. Holtzman,et al.  TREM2 lipid sensing sustains microglia response in an Alzheimer’s disease model , 2015, Cell.

[32]  C. Belmonte,et al.  TRPA1 channels mediate acute neurogenic inflammation and pain produced by bacterial endotoxins , 2014, Nature Communications.

[33]  F. Ginhoux,et al.  Origin of the lamina propria dendritic cell network. , 2009, Immunity.

[34]  M. Diamond,et al.  IL-34 is a tissue-restricted ligand of CSF1R required for the development of Langerhans cells and microglia , 2012, Nature Immunology.

[35]  R. Vance,et al.  Lethal inflammasome activation by a multi-drug resistant pathobiont upon antibiotic disruption of the microbiota , 2012, Nature Medicine.

[36]  T. Powley,et al.  Macrophages Associated with the Intrinsic and Extrinsic Autonomic Innervation of the Rat Gastrointestinal Tract , 2012, Autonomic Neuroscience.

[37]  Joshua D. Meisel,et al.  Chemosensation of Bacterial Secondary Metabolites Modulates Neuroendocrine Signaling and Behavior of C. elegans , 2014, Cell.

[38]  F. Helmchen,et al.  Resting Microglial Cells Are Highly Dynamic Surveillants of Brain Parenchyma in Vivo , 2005, Science.

[39]  S. Yamato,et al.  Possible involvement of muscularis resident macrophages in impairment of interstitial cells of Cajal and myenteric nerve systems in rat models of TNBS-induced colitis , 2006, Histochemistry and Cell Biology.

[40]  Ruslan Medzhitov,et al.  Disease Tolerance as a Defense Strategy , 2012, Science.

[41]  Hidde L Ploegh,et al.  CX3CR1-Mediated Dendritic Cell Access to the Intestinal Lumen and Bacterial Clearance , 2005, Science.

[42]  Ruslan Medzhitov,et al.  Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis , 2004, Cell.

[43]  L. Öhman,et al.  Pathogenesis of IBS: role of inflammation, immunity and neuroimmune interactions , 2010, Nature Reviews Gastroenterology &Hepatology.

[44]  N. Renier,et al.  iDISCO: A Simple, Rapid Method to Immunolabel Large Tissue Samples for Volume Imaging , 2014, Cell.

[45]  A. Keller,et al.  Beta2‐adrenergic receptor signaling in CD4+ Foxp3+ regulatory T cells enhances their suppressive function in a PKA‐dependent manner , 2013, European journal of immunology.

[46]  J. Furness,et al.  II. The intestine as a sensory organ: neural, endocrine, and immune responses. , 1999, American journal of physiology. Gastrointestinal and liver physiology.

[47]  G. Friedlander,et al.  Macrophage-restricted interleukin-10 receptor deficiency, but not IL-10 deficiency, causes severe spontaneous colitis. , 2014, Immunity.

[48]  Anjali A. Sarkar,et al.  Expression of Hand2 is sufficient for neurogenesis and cell type–specific gene expression in the enteric nervous system , 2007, Developmental dynamics : an official publication of the American Association of Anatomists.

[49]  W. Gan,et al.  ATP mediates rapid microglial response to local brain injury in vivo , 2005, Nature Neuroscience.

[50]  S. Hwang,et al.  Bacteria activate sensory neurons that modulate pain and inflammation , 2013, Nature.

[51]  M. Nussenzweig,et al.  Intestinal monocytes and macrophages are required for T cell polarization in response to Citrobacter rodentium , 2013, The Journal of experimental medicine.

[52]  H. Besedovsky,et al.  Sympathetic Nervous System-Immune Interactions in Autoimmune Lymphoproliferative Diseases , 2008, Neuroimmunomodulation.

[53]  S. Lira,et al.  Luminal bacteria recruit CD103+ dendritic cells into the intestinal epithelium to sample bacterial antigens for presentation. , 2013, Immunity.

[54]  J. Ragoussis,et al.  Identification and characterization of enhancers controlling the inflammatory gene expression program in macrophages. , 2010, Immunity.

[55]  G. Pullinger,et al.  6-hydroxydopamine-mediated release of norepinephrine increases faecal excretion of Salmonella enterica serovar Typhimurium in pigs , 2010, Veterinary research.

[56]  S. Kunkel,et al.  Endogenous norepinephrine regulates tumor necrosis factor-alpha production from macrophages in vitro. , 1994, Journal of immunology.

[57]  R. Blakely,et al.  Dependence of Serotonergic and Other Nonadrenergic Enteric Neurons on Norepinephrine Transporter Expression , 2010, The Journal of Neuroscience.

[58]  B. Pulendran,et al.  Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17–producing T cell responses , 2007, Nature Immunology.