TY - JOUR
T1 - Advancements in 3D models for studying human iPSC-microglia
T2 - Insights into neurodevelopment and neurological disorders
AU - Tiwari, Satish Kumar
AU - Ginhoux, Florent
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Microglia are immune cells of the central nervous system, playing a vital role in brain development, homeostasis, and disease. When these cells become dysfunctional, they can contribute to various psychiatric disorders and neurodegenerative diseases. To enhance our understanding of microglial function, researchers are increasingly employing human cell-based models. This approach significantly improves our investigations into these complex conditions and aids in ongoing drug development efforts. In vitro models of human microglia, derived from disease-specific induced pluripotent stem cells (iPSCs), are essential for examining their roles in neurological disorders. These models provide a controlled environment for studying the cellular and molecular processes involved in microglia-driven neuroinflammation and neurodegeneration. Integrating microglia into three-dimensional (3D) organoid cultures yields a more physiologically relevant model of the human brain, thereby advancing the study of brain development and the pathology of neurological disorders. Currently, brain organoid models are limited by the absence of key components, such as vasculature, which restricts their growth and hinders the optimal modeling of neurodevelopment, as well as the examination of microglial forms and functions. This review explores newly developed 3D models for generating human-induced microglia and investigates the potential of these in vitro systems to improve our understanding of brain development and the disorders that emerge from its disruption.
AB - Microglia are immune cells of the central nervous system, playing a vital role in brain development, homeostasis, and disease. When these cells become dysfunctional, they can contribute to various psychiatric disorders and neurodegenerative diseases. To enhance our understanding of microglial function, researchers are increasingly employing human cell-based models. This approach significantly improves our investigations into these complex conditions and aids in ongoing drug development efforts. In vitro models of human microglia, derived from disease-specific induced pluripotent stem cells (iPSCs), are essential for examining their roles in neurological disorders. These models provide a controlled environment for studying the cellular and molecular processes involved in microglia-driven neuroinflammation and neurodegeneration. Integrating microglia into three-dimensional (3D) organoid cultures yields a more physiologically relevant model of the human brain, thereby advancing the study of brain development and the pathology of neurological disorders. Currently, brain organoid models are limited by the absence of key components, such as vasculature, which restricts their growth and hinders the optimal modeling of neurodevelopment, as well as the examination of microglial forms and functions. This review explores newly developed 3D models for generating human-induced microglia and investigates the potential of these in vitro systems to improve our understanding of brain development and the disorders that emerge from its disruption.
KW - iPSC
KW - induced pluripotent stem cells
KW - macrophage
KW - microglia
KW - organoids
UR - http://www.scopus.com/inward/record.url?scp=105000045393&partnerID=8YFLogxK
U2 - 10.1016/j.hlife.2025.02.002
DO - 10.1016/j.hlife.2025.02.002
M3 - Review article
AN - SCOPUS:105000045393
SN - 2949-9283
JO - hLife
JF - hLife
ER -