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纹状体投射神经元在大鼠脑内的生成可延续至新生儿期。

Generation of striatal projection neurons extends into the neonatal period in the rat brain.

机构信息

Centre for Neuroscience, University of Melbourne, Parkville, Australia.

出版信息

J Physiol. 2013 Jan 1;591(1):67-76. doi: 10.1113/jphysiol.2012.246397. Epub 2012 Nov 5.

DOI:10.1113/jphysiol.2012.246397
PMID:23129797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3630772/
Abstract

Substantial advances have been made in the last decade on our understanding of the basic physiology underlying neurogenesis in the postnatal mammalian brain. The bulk of the work in this area has been based on analysis of the adult brain. Relatively less is known about the capacity for neurogenesis in specific structures within the neonatal brain. Here we report that the production of medium spiny striatal projection neurons extends into the early neonatal period under normal physiological conditions in the rat brain. Birth-dating of newborn cells with bromodeoxyuridine at postnatal days 0, 2 and 5 showed a peak production close to birth, which sharply declined at the later time-points. Additionally, there was a low-level but stable contribution of neurons with interneuron identity over the same time-period. Importantly, retroviral labelling of new striatal projection neurons with green fluorescent protein showed long-term survival and terminal differentiation with characteristic morphology, including highly elaborated spiny dendrites, and appropriate axonal targeting of the globus pallidus and midbrain. This latent period of striatal neurogenesis in the early neonatal brain represents an interesting target for regenerative approaches aimed at restoring striatal circuitry in perinatal pathologies, such as hypoxic and ischaemic damage associated with cerebral palsy.

摘要

在过去十年中,我们对哺乳动物大脑中神经发生的基本生理学有了实质性的认识。该领域的大部分工作都是基于对成年大脑的分析。相对而言,对于新生儿大脑中特定结构的神经发生能力了解较少。在这里,我们报告说,在正常生理条件下,大鼠大脑中的中脑纹状体投射神经元的产生会延伸到新生儿早期。在出生后第 0、2 和 5 天用溴脱氧尿苷对新生细胞进行出生标记,显示出接近出生时的高峰产生,而在稍后的时间点急剧下降。此外,在同一时期,神经元的中间神经元特性也有一个低水平但稳定的贡献。重要的是,用绿色荧光蛋白对新生纹状体投射神经元进行逆转录病毒标记显示出长期存活和终末分化,具有特征性的形态,包括高度发达的棘突树突和苍白球和中脑的适当轴突靶向。新生儿早期大脑中的这种纹状体神经发生的潜伏期是一个有趣的目标,适用于再生方法,旨在恢复围产期病理(如脑瘫相关的缺氧和缺血性损伤)中的纹状体回路。

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本文引用的文献

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Cell therapy for neonatal hypoxia-ischemia and cerebral palsy.细胞治疗新生儿缺氧缺血性脑病与脑瘫。
Ann Neurol. 2012 May;71(5):589-600. doi: 10.1002/ana.22670.
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Reduced proliferation in the adult mouse subventricular zone increases survival of olfactory bulb interneurons.成年小鼠侧脑室下区增殖减少可增加嗅球中间神经元的存活。
PLoS One. 2012;7(2):e31549. doi: 10.1371/journal.pone.0031549. Epub 2012 Feb 21.
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Induction of striatal neurogenesis enhances functional recovery in an adult animal model of neonatal hypoxic-ischemic brain injury.诱导纹状体神经发生增强了新生缺氧缺血性脑损伤成年动物模型的功能恢复。
Neuroscience. 2010 Aug 11;169(1):259-68. doi: 10.1016/j.neuroscience.2010.04.038.
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Changing numbers of neuronal and non-neuronal cells underlie postnatal brain growth in the rat.神经元和非神经元细胞数量的变化是大鼠出生后脑生长的基础。
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