Department of Neurobiology, Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
German Center for Neurodegenerative Disease, 81377 Munich, Germany.
J Neurosci. 2020 Aug 19;40(34):6503-6521. doi: 10.1523/JNEUROSCI.3006-19.2020. Epub 2020 Jul 13.
Microglia, a resident CNS macrophage, are dynamic cells, constantly extending and retracting their processes as they contact and functionally regulate neurons and other glial cells. There is far less known about microglia-vascular interactions, particularly under healthy steady-state conditions. Here, we use the male and female mouse cerebral cortex to show that a higher percentage of microglia associate with the vasculature during the first week of postnatal development compared with older ages and that the timing of these associations is dependent on the fractalkine receptor (CX3CR1). Similar developmental microglia-vascular associations were detected in the human brain. Using live imaging in mice, we found that juxtavascular microglia migrated when microglia are actively colonizing the cortex and became stationary by adulthood to occupy the same vascular space for nearly 2 months. Further, juxtavascular microglia at all ages associate with vascular areas void of astrocyte endfeet, and the developmental shift in microglial migratory behavior along vessels corresponded to when astrocyte endfeet more fully ensheath vessels. Together, our data provide a comprehensive assessment of microglia-vascular interactions. They support a mechanism by which microglia use the vasculature to migrate within the developing brain parenchyma. This migration becomes restricted on the arrival of astrocyte endfeet such that juxtavascular microglia become highly stationary and stable in the mature cortex. We report the first extensive analysis of juxtavascular microglia in the healthy, developing, and adult brain. Live imaging revealed that juxtavascular microglia within the cortex are highly motile and migrate along vessels as they are colonizing cortical regions. Using confocal, expansion, super-resolution, and electron microscopy, we determined that microglia associate with the vasculature at all ages in areas lacking full astrocyte endfoot coverage and motility of juxtavascular microglia ceases as astrocyte endfeet more fully ensheath the vasculature. Our data lay the fundamental groundwork to investigate microglia-astrocyte cross talk and juxtavascular microglial function in the healthy and diseased brain. They further provide a potential mechanism by which vascular interactions facilitate microglial colonization of the brain to later regulate neural circuit development.
小胶质细胞是中枢神经系统的固有巨噬细胞,是一种动态细胞,在与神经元和其他神经胶质细胞接触并发挥功能调节作用时,会不断伸展和回缩其突起。相比之下,人们对小胶质细胞与血管的相互作用知之甚少,尤其是在健康的稳态条件下。在这里,我们使用雄性和雌性小鼠大脑皮层来表明,与老年相比,小胶质细胞在出生后发育的第一周内与血管的关联比例更高,并且这些关联的时间取决于 fractalkine 受体(CX3CR1)。在人类大脑中也检测到了类似的发育中小胶质细胞与血管的关联。通过在小鼠中进行活体成像,我们发现,当小胶质细胞积极定植皮层时,靠近血管的小胶质细胞会迁移,并在成年后静止,占据相同的血管空间近 2 个月。此外,所有年龄段的靠近血管的小胶质细胞都与缺乏星形胶质细胞终足的血管区域相关联,并且小胶质细胞沿着血管迁移的发育转变与星形胶质细胞终足更完全包绕血管的时间相对应。总之,我们的数据提供了对小胶质细胞与血管相互作用的全面评估。它们支持一种机制,即小胶质细胞利用血管在发育中的脑实质内迁移。这种迁移在星形胶质细胞终足到达时受到限制,使得靠近血管的小胶质细胞在成熟皮层中变得高度静止和稳定。我们报告了健康、发育中和成年大脑中靠近血管的小胶质细胞的首次广泛分析。活体成像显示,在皮层内的靠近血管的小胶质细胞具有高度的运动性,并沿着血管迁移,因为它们正在定植皮层区域。通过共聚焦、扩展、超分辨率和电子显微镜,我们确定在所有年龄段,小胶质细胞都与血管相关联,在没有完全覆盖星形胶质细胞终足的区域,并且靠近血管的小胶质细胞的运动性随着星形胶质细胞终足更完全地包绕血管而停止。我们的数据为研究健康和患病大脑中小胶质细胞-星形胶质细胞的相互作用和靠近血管的小胶质细胞功能奠定了基础。它们进一步提供了一种潜在的机制,即血管相互作用促进小胶质细胞对大脑的定植,以进一步调节神经回路的发育。