Entry and distribution of microglial cells in human embryonic and fetal cerebral cortex

被引:185
作者
Monier, Anne
Adle-Biassette, Homa
Delezoide, Anne-Lise
Evrard, Philippe
Gressens, Pierre
Verney, Catherine
机构
[1] Univ Paris 07, INSERM U676, F-75221 Paris 05, France
[2] Hop Robert Debre, AP HP, Serv Anat Pathol, F-75019 Paris, France
[3] Hop Bichat Claude Bernard, AP HP, Serv Anat Pathol, F-75877 Paris 18, France
关键词
brain macrophages; CD45; development; Iba1; immunocytochemistry; proliferation marker; vessels;
D O I
10.1097/nen.0b013e3180517b46
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Microglial cells penetrate into and scatter throughout the human cortical grey and white matter according to a specific spatiotemporal pattern during the first 2 trimesters of gestation. Routes of entry were quantitatively and qualitatively different from those identified in the diencephalon. Starting at 4.5 gestational weeks, amoeboid microglial cells, characterized by different antibodies as Iba1, CD68, CD45, and MHC-II, entered the cerebral wall from the ventricular lumen and the leptomeninges. Migration was mainly radial and tangential toward the immature white matter, subplate layer, and cortical plate, whereas pial cells populated the prospective layer I. The intraparenchymal vascular route of entry was detectable only from 12 gestational weeks. Interestingly, microglial cells accumulated in restricted laminar bands particularly at 19, to 24 gestational weeks among the corona radiata fibers rostrally, extending caudally in the immature white matter to reach the visual radiations. This accumulation of proliferating MIBI-positive microglia (as shown by MIB1-Iba1 double immunolabeling) was located at the site of white matter injury in premature neonates. The spatiotemporal organization of microglia in the immature white and grey matter suggests that these cells may play active roles in developmental processes and in injury to the developing brain.
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页码:372 / 382
页数:11
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