Fibromyalgia and microglial TNF-α: Translational research using human blood induced microglia-like cells

Masahiro Ohgidani1, Takahiro A Kato2, Masako Hosoi3

  • 1Department of Neuropsychiatry, Graduate School of Medical Sciences, Kyushu University, Maidashi 3-1-1, Higashi-ku, Fukuoka, 812-8582, Japan.

Scientific Reports
|September 21, 2017
PubMed

Insights

Fibromyalgia patients show hypersensitive microglia, immune cells in the brain. Increased tumor necrosis factor-alpha (TNF-α) in these cells may explain chronic pain and psychological symptoms in fibromyalgia.

Area of Science:

  • Neuroimmunology
  • Cellular Biology

Background:

  • Fibromyalgia is a complex condition causing chronic pain and psychological distress.
  • The exact pathology remains unclear, but microglia activation in the brain is a suspected factor.
  • Research on human microglia has been limited by technological and ethical challenges.

Purpose of the Study:

  • To investigate the role of human microglia in fibromyalgia.
  • To compare the activation status of microglia between fibromyalgia patients and healthy individuals using a novel cell model.

Main Methods:

  • Developed human-induced microglia-like (iMG) cells from peripheral blood monocytes of 14 fibromyalgia patients and 10 healthy controls.
  • Compared ATP-stimulated iMG cell activation, specifically tumor necrosis factor-alpha (TNF-α) expression at mRNA and protein levels.

Main Results:

  • Significantly increased TNF-α expression in ATP-stimulated iMG cells from fibromyalgia patients compared to healthy controls.
  • Moderate correlation observed between elevated TNF-α levels and clinical fibromyalgia symptoms, including pain and mental health manifestations.
  • Suggests microglia in fibromyalgia patients are hypersensitive to ATP stimulation.

Conclusions:

  • Human microglia, modeled as iMG cells, exhibit heightened activation in fibromyalgia patients.
  • Increased TNF-α production by microglia may be a key contributor to fibromyalgia's complex pathology.
  • This study provides a novel cellular model for investigating fibromyalgia mechanisms and potential therapeutic targets.