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人胼胝体发育过程中神经元的形态、分子表型和分布。

Morphology, molecular phenotypes and distribution of neurons in developing human corpus callosum.

机构信息

Croatian Institute for Brain Research, University of Zagreb, Šalata 12, 10000 Zagreb, Croatia.

出版信息

Eur J Neurosci. 2010 Nov;32(9):1423-32. doi: 10.1111/j.1460-9568.2010.07400.x. Epub 2010 Sep 16.

Abstract

The aim of this study was to investigate the morphology, molecular phenotypes, distribution and developmental history of interstitial neurons in the human corpus callosum, here defined as intracallosal neurons. We analysed 26 fetuses, three newborns, five infants and children, and eight adults [age range - 15 weeks postconception (PCW) to 59 years] by means of acetylcholinesterase (AChE) histochemistry and immunohistochemistry for neuron markers (MAP2, NeuN, NPY, calretinin and calbindin). We found a heterogeneous neuron population, positioned within the callosal trunk itself (aside from neurons present in the transient midline structures such as callosal sling, septa or subcallosal zone), which was most numerous during the second half of gestation and early postnatal years. We named these cells intracallosal neurons. At 15 PCW, the intracallosal neuron population consisted of poorly differentiated, small fusiform or bipolar, migratory-like MAP2- or calretinin-positive neurons which could be observed until mid-gestation. Later the population comprised morphologically diverse, predominantly well-differentiated MAP2-, NPY-, calbindin- and AChE-positive neurons. The morphological differentiation of intracallosal neurons culminated in the newborns and remained pronounced in infants and children. In the adult brain, the intracallosal neurons were found only sporadically, with small somata and poorly stained dendrites. Thus, intracallosal neurons form part of a transitory neuron population with a developmental peak contemporaneous to the critical period of callosal formation. Therefore, they may be involved in processes such as axon guiding or elongation, withdrawal of exuberant axons, fasciculation, or functional tuning, which occur at that time.

摘要

本研究旨在探讨人胼胝体内(定义为胼胝体内神经元)间质神经元的形态、分子表型、分布和发育史。我们通过乙酰胆碱酯酶(AChE)组织化学和神经元标志物(MAP2、NeuN、NPY、钙视网膜蛋白和钙结合蛋白)免疫组织化学分析了 26 例胎儿、3 例新生儿、5 例婴儿和儿童以及 8 例成人(年龄范围为受精后 15 周(PCW)至 59 岁)。我们发现了一个异质的神经元群体,位于胼胝体干本身内(除了存在于胼胝体吊带、隔或胼胝下区等短暂中线结构中的神经元之外),该群体在妊娠后半期和出生后早期最为丰富。我们将这些细胞命名为胼胝体内神经元。在 15 PCW 时,胼胝体内神经元群体由分化不良的小梭形或双极、迁移样 MAP2 或钙视网膜蛋白阳性神经元组成,这些神经元可以观察到中期妊娠。后来,该群体包括形态多样、主要分化良好的 MAP2、NPY、钙结合蛋白和 AChE 阳性神经元。胼胝体内神经元的形态分化在新生儿达到高峰,并在婴儿和儿童中仍然明显。在成人大脑中,胼胝体内神经元仅零星存在,胞体较小,树突染色不良。因此,胼胝体内神经元是具有发育高峰期的短暂神经元群体的一部分,与胼胝体形成的关键期同时发生。因此,它们可能参与了轴突引导或伸长、多余轴突的撤回、聚集或功能调谐等过程,这些过程发生在那个时期。

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