Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024:37:545-568.
doi: 10.1007/978-3-031-55529-9_30.

Emerging Models to Study Human Microglia In vitro

Affiliations
Review

Emerging Models to Study Human Microglia In vitro

Henna Jäntti et al. Adv Neurobiol. 2024.

Abstract

New in vitro models provide an exciting opportunity to study live human microglia. Previously, a major limitation in understanding human microglia in health and disease has been their limited availability. Here, we provide an overview of methods to obtain human stem cell or blood monocyte-derived microglia-like cells that provide a nearly unlimited source of live human microglia for research. We address how understanding microglial ontogeny can help modeling microglial identity and function in a dish with increased accuracy. Moreover, we categorize stem cell-derived differentiation methods into embryoid body based, growth factor driven, and coculture-driven approaches, and review novel viral approaches to reprogram stem cells directly into microglia-like cells. Furthermore, we review typical readouts used in the field to verify microglial identity and characterize functional microglial phenotypes. We provide an overview of methods used to study microglia in environments more closely resembling the (developing) human CNS, such as cocultures and brain organoid systems with incorporated or innately developing microglia. We highlight how microglia-like cells can be utilized to reveal molecular and functional mechanisms in human disease context, focusing on Alzheimer's disease and other neurodegenerative diseases as well as neurodevelopmental diseases. Finally, we provide a critical overview of challenges and future opportunities to more accurately model human microglia in a dish and conclude that novel in vitro microglia-like cells provide an exciting potential to bring preclinical research of microglia to a new era.

Keywords: Authors Henna Jäntti and Lois Kistemaker have equally contributed to this chapter.; Brain organoid; In vitro model; Microglia; Monocyte; iPSC.

PubMed Disclaimer

Similar articles

References

    1. Abud EM, Ramirez RN, Martinez ES et al (2017) iPSC-derived human microglia-like cells to study neurological diseases. Neuron 94:278–293.e9. https://doi.org/10.1016/j.neuron.2017.03.042 - DOI - PubMed - PMC
    1. Akiyama H, Jalloh S, Park S et al (2021) Expression of HIV-1 intron-containing RNA in microglia induces inflammatory responses. J Virol 95(5):e01386-20. https://doi.org/10.1128/JVI - DOI - PubMed - PMC
    1. Albert K, Niskanen J, Kälvälä S, Lehtonen Š (2021) Utilising induced pluripotent stem cells in neurodegenerative disease research: focus on glia. Int J Mol Sci 22. https://doi.org/10.3390/ijms22094334
    1. Allison RL, Adelman JW, Abrudan J et al (2022) Microglia influence neurofilament deposition in ALS iPSC-derived motor neurons. Genes 13(13):241. https://doi.org/10.3390/GENES13020241 - DOI - PubMed - PMC
    1. Alsema AM, Jiang Q, Kracht L et al (2020) Profiling microglia from Alzheimer’s disease donors and non-demented elderly in acute human postmortem cortical tissue. Front Mol Neurosci 13:134. https://doi.org/10.3389/FNMOL.2020.00134/BIBTEX - DOI - PubMed - PMC

MeSH terms