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MRI 可视化内源性神经祖细胞沿成年鼠脑内 RMS 的迁移:各种 MPIPO 标记策略的验证。

MRI visualization of endogenous neural progenitor cell migration along the RMS in the adult mouse brain: validation of various MPIO labeling strategies.

机构信息

Bio-Imaging Lab, Department of Biomedical Sciences, University of Antwerp, B-2020 Antwerp, Belgium.

出版信息

Neuroimage. 2010 Feb 1;49(3):2094-103. doi: 10.1016/j.neuroimage.2009.10.034. Epub 2009 Oct 19.

Abstract

The adult rodent brain contains neural progenitor cells (NPCs), generated in the subventricular zone (SVZ), which migrate along the rostral migratory stream (RMS) towards the olfactory bulb (OB) where they differentiate into neurons. The aim of this study was to visualize endogenous NPC migration along the RMS with magnetic resonance imaging (MRI) in adult healthy mice. We evaluated various in situ (in vivo) labeling approaches using micron-sized iron oxide particles (MPIOs) on their efficiency to label endogenous NPCs. In situ labeling and visualization of migrating NPCs were analyzed by a longitudinal MRI study and validated with histology. Here, we visualized endogenous NPC migration in the mouse brain by in vivo MRI and demonstrated accumulation of MPIO-labeled NPCs in the OB over time with ex vivo MRI. Furthermore, we investigated the influence of in situ injection of MPIOs on adult neurogenesis. Quantitative analysis of bromodeoxyuridine labeled cells revealed altered proliferation in the SVZ and NPC migration after in situ MPIO injection. From the labeling strategies presented in this report, intraventricular injection of a small number of MPIOs combined with the transfection agent poly-l-lysine hydrobromide was the best method as labeling of the NPCs was successful and proliferation in the SVZ was only marginally affected. While MRI visualization of endogenous NPC migration can provide insight into aberrant NPC migration in disease models, this work emphasizes the importance to carefully explore the impact on adult neurogenesis when new in situ labeling strategies are developed.

摘要

成年啮齿动物大脑中含有神经祖细胞(NPCs),这些细胞产生于侧脑室下区(SVZ),并沿着前脑腹侧迁移流(RMS)迁移到嗅球(OB),在那里分化为神经元。本研究旨在通过磁共振成像(MRI)在成年健康小鼠中可视化内源性 NPC 沿着 RMS 的迁移。我们评估了使用微米级氧化铁颗粒(MPIO)进行的各种原位(体内)标记方法,以评估其标记内源性 NPC 的效率。通过纵向 MRI 研究分析了原位标记和迁移 NPC 的可视化,并通过组织学进行了验证。在这里,我们通过体内 MRI 可视化了小鼠大脑中的内源性 NPC 迁移,并通过离体 MRI 证明了随着时间的推移,MPIO 标记的 NPC 逐渐积累到 OB 中。此外,我们还研究了原位注射 MPIO 对成年神经发生的影响。溴脱氧尿苷标记细胞的定量分析显示,原位 MPIO 注射后 SVZ 中的增殖和 NPC 迁移发生改变。从本报告中提出的标记策略来看,脑室注射少量 MPIO 并结合转染试剂聚赖氨酸氢溴酸盐是最好的方法,因为 NPC 的标记是成功的,而 SVZ 中的增殖仅受到轻微影响。虽然内源性 NPC 迁移的 MRI 可视化可以提供对疾病模型中异常 NPC 迁移的深入了解,但这项工作强调了在开发新的原位标记策略时,仔细探索对成年神经发生影响的重要性。

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