Foxp3+IL-17+ T cells promote development of cancer-initiating cells in colorectal cancer

J Leukoc Biol. 2011 Jan;89(1):85-91. doi: 10.1189/jlb.0910506. Epub 2010 Oct 15.

Abstract

The pathogenesis of CRC remains to be further understood. This study was designed to elucidate the role of Foxp3+IL-17+ T cells in the pathogenesis of CRC. Surgically removed CRC tissue was collected from 12 patients with CRC. The frequency and cytokine profile of Foxp3+IL-17+ T cells in CRC were examined by flow cytometry. Chemokine CXCL11 was examined in CRC tissue by Western blotting. Treg chemotaxis was examined in a transwell system. The effect of Foxp3+IL-17+ T cells on induction of cancer-initiating cells was examined; the latter's Akt and MAPK activities and colony formation were examined afterward. Abundant Foxp3+IL-17+ T cells were detected in CRC tissue that expresses high levels of TGF-β, CXCR3, CCR6, and RORγt. High levels of CXCL11 were detected in CRC tissue-derived CD68+ cells, which had a strong chemotactic effect on Foxp3+ Tregs. Hypoxia induced the expression of IL-17 in Foxp3+ Tregs; Foxp3+IL-17+ T cells were capable of inducing CRC-associated cell markers in BMMo and drove the cells to be cancer-initiating cells. High levels of phosphorylated Akt and MAPK were detected in the induced cancer-initiation cells; the latter has the capability to form a colony. CRC tissue-derived Foxp3+IL-17+ cells have the capacity to induce cancer-initiating cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Biomarkers, Tumor / metabolism
  • Cell Hypoxia
  • Chemokine CXCL11 / metabolism
  • Chemotaxis
  • Colorectal Neoplasms / enzymology
  • Colorectal Neoplasms / immunology*
  • Colorectal Neoplasms / pathology
  • Female
  • Forkhead Transcription Factors / immunology*
  • Humans
  • Interleukin-17 / immunology*
  • Macrophages / metabolism
  • Male
  • Middle Aged
  • Mitogen-Activated Protein Kinases / metabolism
  • Neoplastic Stem Cells / immunology*
  • Neoplastic Stem Cells / pathology
  • Proto-Oncogene Proteins c-akt / metabolism
  • T-Lymphocytes / enzymology
  • T-Lymphocytes / immunology*
  • T-Lymphocytes, Regulatory / cytology
  • T-Lymphocytes, Regulatory / immunology

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers, Tumor
  • CD68 antigen, human
  • CXCL11 protein, human
  • Chemokine CXCL11
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Interleukin-17
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinases