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Updated: Oct 19, 2025

Isolation of Cortical Microglia with Preserved Immunophenotype and Functionality From Murine Neonates
Published on: January 30, 2014
The behavior and functions of embryonic microglia
1Department of Anatomy and Cell Biology, Graduate School of Medicine, Nagoya University, 65 Tsurumai, Showa, Nagoya, Aichi, 466-8550, Japan. ha-yuki@med.nagoya-u.ac.jp.
Abstract:
Microglia are the resident immune cells of the central nervous system. Microglial progenitors are generated in the yolk sac during the early embryonic stage. Once microglia enter the brain primordium, these cells colonize the structure through migration and proliferation during brain development. Microglia account for a minor population among the total cells that constitute the developing cortex, but they can associate with many surrounding neural lineage cells by extending their filopodia and through their broad migration capacity. Of note, microglia change their distribution in a stage-dependent manner in the developing brain: microglia are homogenously distributed in the pallium in the early and late embryonic stages, whereas these cells are transiently absent from the cortical plate (CP) from embryonic day (E) 15 to E16 and colonize the ventricular zone (VZ), subventricular zone (SVZ), and intermediate zone (IZ). Previous studies have reported that microglia positioned in the VZ/SVZ/IZ play multiple roles in neural lineage cells, such as regulating neurogenesis, cell survival and neuronal circuit formation. In addition to microglial functions in the zones in which microglia are replenished, these cells indirectly contribute to the proper maturation of post-migratory neurons by exiting the CP during the mid-embryonic stage. Overall, microglial time-dependent distributional changes are necessary to provide particular functions that are required in specific regions. This review summarizes recent advances in the understanding of microglial colonization and multifaceted functions in the developing brain, especially focusing on the embryonic stage, and discuss the molecular mechanisms underlying microglial behaviors.
Insights
Microglia, the brain's immune cells, migrate and proliferate during development. Their changing distribution is crucial for regulating neurogenesis and neuronal maturation in the embryonic brain.
Area of Science:
- Neuroscience
- Immunology
- Developmental Biology
Background:
- Microglia are the primary immune cells within the central nervous system.
- Microglial progenitors originate in the yolk sac and migrate to colonize the developing brain.
- These cells interact with neural lineage cells through filopodia extension and migration.
Purpose of the Study:
- To review recent advancements in understanding microglial colonization and functions during embryonic brain development.
- To focus on the dynamic distribution of microglia and their roles in specific brain regions.
- To discuss the molecular mechanisms governing microglial behavior in the developing brain.
Main Methods:
- This is a review article, synthesizing existing research.
- Focuses on analyzing stage-dependent microglial distribution patterns.
- Examines reported functions of microglia in different embryonic brain zones.
Main Results:
- Microglia exhibit stage-dependent distribution changes in the embryonic brain.
- They are homogenously distributed early on, then absent from the cortical plate (CP) from E15-E16, colonizing the ventricular zone (VZ), subventricular zone (SVZ), and intermediate zone (IZ).
- Microglia in the VZ/SVZ/IZ regulate neurogenesis, cell survival, and circuit formation, indirectly aiding post-migratory neuron maturation.
Conclusions:
- Time-dependent microglial distributional shifts are essential for specific regional functions during brain development.
- Microglia play multifaceted roles, influencing neural lineage cells and neuronal maturation.
- Understanding the molecular basis of microglial behavior is key to comprehending embryonic brain development.
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