Format

Send to

Choose Destination
Endocrinology. 2018 May 1;159(5):2241-2252. doi: 10.1210/en.2018-00053.

Regulation of Intracellular Triiodothyronine Is Essential for Optimal Macrophage Function.

Author information

1
Department of Endocrinology and Metabolism, Academic Medical Center, University of Amsterdam, AZ Amsterdam, Netherlands.
2
Department of Neurology, Academic Medical Center, University of Amsterdam, Amsterdam Neuroscience, AZ Amsterdam, Netherlands.
3
Department of Medical Microbiology and Infection Control, VU University Medical Center, HV Amsterdam, Netherlands.
4
Department of Immunology, Erasmus University Medical Center, CE Rotterdam, Netherlands.
5
Department of Molecular Medicine, Maine Medical Center Research Institute, Maine Medical Center, Scarborough, Maine.

Abstract

Innate immune cells, including macrophages, have recently been identified as target cells for thyroid hormone. We hypothesized that optimal intracellular concentrations of the active thyroid hormone triiodothyronine (T3) are essential for proinflammatory macrophage function. T3 is generated intracellularly by type 2 deiodinase (D2) and acts via the nuclear thyroid hormone receptor (TR). In zebrafish embryos, D2 knockdown increased mortality during pneumococcal meningitis. Primary murine D2 knockout macrophages exhibited impaired phagocytosis and partially reduced cytokine response to stimulation with bacterial endotoxin. These effects are presumably due to reduced intracellular T3 availability. Knockdown of the main TR in macrophages, TRα, impaired polarization into proinflammatory macrophages and amplified polarization into immunomodulatory macrophages. Intracellular T3 availability and action appear to play a crucial role in macrophage function. Our data suggest that low intracellular T3 action has an anti-inflammatory effect, possibly due to an effect on macrophage polarization mediated via the TRα. This study provides important insights into the link between the endocrine and innate immune system.

PMID:
29648626
PMCID:
PMC5920313
DOI:
10.1210/en.2018-00053
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Silverchair Information Systems Icon for PubMed Central
Loading ...
Support Center