The migration speed of cancer cells influenced by macrophages and myofibroblasts co-cultured in a microfluidic chip

Integr Biol (Camb). 2012 Feb;4(2):177-82. doi: 10.1039/c2ib00112h. Epub 2011 Dec 16.

Abstract

We employ a microfluidic chip with three culture chambers to investigate the interactions among lung cancer cells, macrophages and myofibroblasts. By mixing the conditioned media of macrophages and myofibroblasts in this chip, we confirm that these two stromal cells have synergistic effects in accelerating the migration of cancer cells. However, as the myofibroblasts are pretreated with the conditioned medium of macrophages, the myofibroblasts' ability to enhance the migration of cancer cells is lowered. The tumour necrosis factor-α produced by macrophages reduces the expression of α-smooth muscle actin and the secretion of transforming growth factor-β1 in myofibroblasts. Once the tumour necrosis factor-α in the macrophage conditioned medium is neutralized, the macrophage medium-pretreated myofibroblasts can still accelerate the migration of cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / immunology
  • Adenocarcinoma / pathology*
  • Cell Communication / physiology*
  • Cell Line, Tumor
  • Cell Movement / physiology*
  • Coculture Techniques
  • Culture Media, Conditioned
  • Humans
  • Lung Neoplasms / immunology
  • Lung Neoplasms / pathology*
  • Macrophages / immunology
  • Macrophages / pathology*
  • Microfluidics / instrumentation
  • Microfluidics / methods
  • Microscopy, Confocal
  • Myofibroblasts / immunology
  • Myofibroblasts / pathology*
  • Transforming Growth Factor beta / immunology
  • Tumor Necrosis Factor-alpha / analysis
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Culture Media, Conditioned
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha