Visualization of T Cell-Regulated Monocyte Clusters Mediating Keratinocyte Death in Acquired Cutaneous Immunity

J Invest Dermatol. 2018 Jun;138(6):1328-1337. doi: 10.1016/j.jid.2018.01.018. Epub 2018 Feb 1.

Abstract

It remains unclear how monocytes are mobilized to amplify inflammatory reactions in T cell-mediated adaptive immunity. Here, we investigate dynamic cellular events in the cascade of inflammatory responses through intravital imaging of a multicolor-labeled murine contact hypersensitivity model. We found that monocytes formed clusters around hair follicles in the contact hypersensitivity model. In this process, effector T cells encountered dendritic cells under regions of monocyte clusters and secreted IFN-γ, which mobilizes CCR2-dependent monocyte interstitial migration and CXCR2-dependent monocyte cluster formation. We showed that hair follicles shaped the inflammatory microenvironment for communication among the monocytes, keratinocytes, and effector T cells. After disrupting the T cell-mobilized monocyte clusters through CXCR2 antagonization, monocyte activation and keratinocyte apoptosis were significantly inhibited. Our study provides a new perspective on effector T cell-regulated monocyte behavior, which amplifies the inflammatory reaction in acquired cutaneous immunity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Video-Audio Media

MeSH terms

  • Adaptive Immunity*
  • Animals
  • Apoptosis / immunology*
  • CD11c Antigen / genetics
  • CX3C Chemokine Receptor 1 / genetics
  • Cell Communication / immunology*
  • Cells, Cultured
  • Dendritic Cells / immunology
  • Dermatitis, Contact / immunology*
  • Dermatitis, Contact / pathology
  • Disease Models, Animal
  • Female
  • Genes, Reporter / genetics
  • Humans
  • Intravital Microscopy / methods
  • Keratinocytes / immunology
  • Luminescent Proteins / genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microscopy, Confocal
  • Monocytes / immunology
  • Oxazolone / administration & dosage
  • Oxazolone / immunology
  • Skin / cytology
  • Skin / immunology
  • Skin / pathology
  • T-Lymphocyte Subsets / immunology*
  • Time-Lapse Imaging

Substances

  • CD11c Antigen
  • CX3C Chemokine Receptor 1
  • Cx3cr1 protein, mouse
  • Luminescent Proteins
  • Oxazolone