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Updated: Oct 12, 2025

Isolation and Culture of Endothelial Cells from the Embryonic Forebrain
Published on: January 23, 2014
Embryonic Pericytes Promote Microglial Homeostasis and Their Effects on Neural Progenitors in the Developing Cerebral
Yuki Hattori1, Haruka Itoh2, Yoji Tsugawa3
1Department of Anatomy and Cell Biology, Graduate School of Medicine, Nagoya University, Nagoya, Aichi 466-8550, Japan ha-yuki@med.nagoya-u.ac.jp.
Abstract:
Multifaceted microglial functions in the developing brain, such as promoting the differentiation of neural progenitors and contributing to the positioning and survival of neurons, have been progressively revealed. Although previous studies have noted the relationship between vascular endothelial cells and microglia in the developing brain, little attention has been given to the importance of pericytes, the mural cells surrounding endothelial cells. In this study, we attempted to dissect the role of pericytes in microglial distribution and function in developing mouse brains. Our immunohistochemical analysis showed that approximately half of the microglia attached to capillaries in the cerebral walls. Notably, a magnified observation of the position of microglia, vascular endothelial cells and pericytes demonstrated that microglia were preferentially associated with pericytes that covered 79.8% of the total capillary surface area. Through in vivo pericyte depletion induced by the intraventricular administration of a neutralizing antibody against platelet-derived growth factor receptor (PDGFR)β (clone APB5), we found that microglial density was markedly decreased compared with that in control antibody-treated brains because of their low proliferative capacity. Moreover, in vitro coculture of isolated CD11b+ microglia and NG2+PDGFRα- cells, which are mostly composed of pericytes, from parenchymal cells indicated that pericytes promote microglial proliferation via the production of soluble factors. Furthermore, pericyte depletion by APB5 treatment resulted in a failure of microglia to promote the differentiation of neural stem cells into intermediate progenitors. Taken together, our findings suggest that pericytes facilitate microglial homeostasis in the developing brains, thereby indirectly supporting microglial effects on neural progenitors.SIGNIFICANCE STATEMENT This study highlights the novel effect of pericytes on microglia in the developing mouse brain. Through multiple analyses using an in vivo pericyte depletion mouse model and an in vitro coculture study of isolated pericytes and microglia from parenchymal cells, we demonstrated that pericytes contribute to microglial proliferation and support microglia in efficiently promoting the differentiation of neural stem cells into intermediate progenitors. Our present data provide evidence that pericytes function not only in the maintenance of cerebral microcirculation and blood brain barrier (BBB) integrity but also in microglial homeostasis in the developing cerebral walls. These findings will expand our knowledge and help elucidate the mechanism of brain development both in healthy and disease conditions.
Insights
Pericytes are crucial for microglial homeostasis in developing brains, promoting microglial proliferation and supporting neural stem cell differentiation. This study reveals their novel role in brain development.
Area of Science:
- Neuroscience
- Developmental Biology
- Cell Biology
Background:
- Microglia play vital roles in the developing brain, including neural progenitor differentiation and neuron survival.
- While endothelial cells and microglia interactions are known, the role of pericytes in this dynamic remains understudied.
Purpose of the Study:
- To investigate the role of pericytes in the distribution and function of microglia within developing mouse brains.
- To elucidate the mechanisms by which pericytes influence microglial proliferation and their support of neural stem cell differentiation.
Main Methods:
- Immunohistochemical analysis to determine microglial association with cerebral capillaries and pericytes.
- In vivo pericyte depletion using an antibody against platelet-derived growth factor receptor (PDGFR)β.
- In vitro co-culture of isolated microglia and pericytes to assess pericyte-mediated microglial proliferation.
Main Results:
- Microglia were found to preferentially associate with pericytes covering cerebral capillaries.
- Pericyte depletion significantly reduced microglial density due to decreased proliferation.
- Pericytes promote microglial proliferation through soluble factors and support neural stem cell differentiation into intermediate progenitors.
Conclusions:
- Pericytes are essential for maintaining microglial homeostasis in the developing brain.
- Pericytes indirectly support microglial functions in neural progenitor differentiation.
- These findings expand the understanding of pericyte functions beyond vascular maintenance to include neurodevelopmental roles.
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