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血管内皮生长因子及其高亲和力受体 (VEGFR-2) 在人类大脑前脑和小脑发育过程中高度表达。

Vascular endothelial growth factor and its high-affinity receptor (VEGFR-2) are highly expressed in the human forebrain and cerebellum during development.

机构信息

Neovasc, Rouen Institute for Medical Research and Innovation, Normandy, France.

出版信息

J Neuropathol Exp Neurol. 2010 Feb;69(2):111-28. doi: 10.1097/NEN.0b013e3181ccc9a9.

Abstract

Vascular endothelial growth factor (VEGF) is an angiogenic and neurotrophic factor in both adult and neonatal animals, but its expression and role have been incompletely studied in the developing human brain. We analyzed the distribution of VEGF and its high-affinity receptor VEGFR-2 in the human forebrain and cerebellum at developmental stages from 14 weeks' gestation (WG) to the13th postnatal month. Tissue samples free of detectable neuropathologic abnormalities were assessed by immunohistochemistry and confocal microscopy using anti-human VEGF and VEGFR-2 antibodies. The VEGFR-2 was first expressed in the whole cerebral mantle and in migrating cells in the intermediate zone, whereas VEGFwas found in superficial layers of the cortical plate, in radial glia, and in the cerebellar external germinal cell layer. From 23 WG, temporospatial VEGFR-2 expression was superimposable on that ofVEGF in the cortical plate, intermediate zone, basal ganglia, limbicstructures, and external germinal cell layer. The VEGF/VEGFR-2-positive astrocytes were observed during their generation and migration from 23 WG to the first postnatal month. The VEGF-positive mature oligodendrocytes were observed in myelinating structures in the forebrain from birth and in the cerebellum from 24WG. These data suggest that VEGF and VEGFR-2 are likely involved in several aspects of human brain development.

摘要

血管内皮生长因子(VEGF)是成年和新生动物中的一种血管生成和神经营养因子,但在发育中的人类大脑中,其表达和作用尚未得到充分研究。我们分析了 VEGF 及其高亲和力受体 VEGFR-2 在 14 周妊娠(WG)至第 13 个出生后月的人类前脑和小脑发育阶段的分布。使用抗人 VEGF 和 VEGFR-2 抗体通过免疫组织化学和共聚焦显微镜分析评估无明显神经病理学异常的组织样本。VEGFR-2 首先在整个大脑皮层和中间带的迁移细胞中表达,而 VEGF 则在前脑皮层的浅层、放射状胶质和小脑外胚层生发细胞层中发现。从 23 WG 开始,皮质板、中间带、基底神经节、边缘结构和外胚层生发细胞层的时空 VEGFR-2 表达与 VEGF 重叠。从 23 WG 到出生后第一个月,可以观察到 VEGF/VEGFR-2 阳性星形胶质细胞的生成和迁移。出生时在前脑的髓鞘形成结构中观察到 VEGF 阳性成熟少突胶质细胞,从 24 WG 开始在小脑观察到。这些数据表明,VEGF 和 VEGFR-2 可能参与了人类大脑发育的几个方面。

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