'Repair' Treg Cells in Tissue Injury

Cell Physiol Biochem. 2017;43(6):2155-2169. doi: 10.1159/000484295. Epub 2017 Oct 25.

Abstract

Studies in mice and humans have elucidated an important role for Tregs in promoting tissue repair and restoring tissue integrity. Emerging evidence has revealed that Tregs promoted wound healing and repair processes at multiple tissue sites, such as the heart, liver, kidney, muscle, lung, bone and central nervous system. The localization of repair Tregs in the lung, muscle and liver exhibited unique phenotypes and functions. Epidermal growth factor receptor, amphiregulin, CD73/CD39 and keratinocyte growth factor are important repair factors that are produced or expressed by repair Tregs; these factors coordinate with parenchymal cells to limit injury and promote repair. In addition, repair Tregs can be modulated by IL-33/ST2, TCR signals and other cytokines in the context of injured microenvironment cues. In this review, we provide an overview of the emerging knowledge about Treg-mediated repair in damaged tissues and organs.

Keywords: Repair; Tissue injury; Treg cells.

Publication types

  • Review

MeSH terms

  • Amphiregulin / metabolism
  • Animals
  • ErbB Receptors / metabolism
  • Fibroblast Growth Factor 7 / metabolism
  • Humans
  • Interleukin-33 / metabolism
  • Myocardial Infarction / immunology
  • Myocardial Infarction / pathology
  • Receptors, Antigen, T-Cell / metabolism
  • Signal Transduction
  • Spinal Cord Injuries / immunology
  • Spinal Cord Injuries / pathology
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / metabolism*

Substances

  • Amphiregulin
  • Interleukin-33
  • Receptors, Antigen, T-Cell
  • Fibroblast Growth Factor 7
  • ErbB Receptors