Introducing directly induced microglia-like (iMG) cells from fresh human monocytes: A novel translational research tool for psychiatric disorders

Masahiro Ohgidani, Takahiro A. Kato, Shigenobu Kanba

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16 Citations (Scopus)

Abstract

Microglia, glial cells with immunological functions, have been implicated in various neurological diseases and psychiatric disorders in rodent studies, and human postmortem and PET studies. However, the deeper molecular implications of living human microglia have not been clarified. Here, we introduce a novel translational research approach focusing on human microglia. We have recently developed a new technique for creating induced microglia-like (iMG) cells from human peripheral blood. Two cytokines, GM-CSF and IL-34, converted human monocytes into the iMG cells within 14 days, which show various microglial characterizations; expressing markers, forming a ramified morphology, and phagocytic activity with various cytokine releases. We have already confirmed the applicability of this technique by analyzing iMG cells from a patient of Nasu-Hakola disease (NHD; Ohgidani et al., 2014). We herein show possible applications of the iMG cells in translational research. We believe that this iMG technique will open the door to explore various unknown dynamic aspects of human microglia in psychiatric disorders. This also opens new routes for psychopharmacological approach such as drug efficacy screening and personalized medicine.

Original languageEnglish
Article number184
JournalFrontiers in Cellular Neuroscience
Volume9
Issue numberMAY
DOIs
Publication statusPublished - May 27 2015

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Translational Medical Research
Microglia
Psychiatry
Monocytes
Cytokines
Precision Medicine
Preclinical Drug Evaluations
Granulocyte-Macrophage Colony-Stimulating Factor
Neuroglia
Rodentia

All Science Journal Classification (ASJC) codes

  • Cellular and Molecular Neuroscience

Cite this

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