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在未受刺激的大鼠和全脑缺血后,蛋白酶激活受体 4 在海马中的细胞表达模式。

Cellular expression pattern of the protease-activated receptor 4 in the hippocampus in naïve rats and after global ischaemia.

机构信息

Leibniz Institute for Neurobiology, Magdeburg, Germany.

出版信息

J Neurosci Res. 2010 Mar;88(4):850-7. doi: 10.1002/jnr.22261.

DOI:10.1002/jnr.22261
PMID:19859967
Abstract

A pronounced hippocampal expression of the Protease-activated Receptor 4 (PAR4) has recently been shown. In the current study the authors define the PAR4-associated sub-cellular structures and the influence of global ischaemia on the expression of PAR4. For that purpose the authors performed double labelling with fluorescence immunohistochemistry on tissue from naïve and post-ischaemic rats. In naïve animals - apart from the expression in granular and pyramidal neurons - there was an intensive lamellar expression of PAR4 in the CA4 region. Further analysis revealed that PAR4 was localised exclusively on mossy fibre axons in CA4 as detected by double-labelling with calbindin D-28k, but there was no overlap with markers of the neuronal cell body, interneurons, and post-synaptic, pre-synaptic and dendritic structures. Three and 14 days post ischaemia, CA1 neurons were degenerated and, consequently, there was no PAR4 signal in the CA1 band. In most other hippocampal structures no change in the PAR4 expression was detectable, with the exception of the CA3 region. Here, the fibre-associated PAR4 signal was diminished and disintegrated post ischaemia. Additionally, a redistribution from the membrane-bound neuronal localisation of PAR4 in control animals to a diffuse localisation all over the cell soma was revealed in the CA3 area 14 days post ischaemia. In conclusion, the current study proves for the first time that PAR4 is localised in mossy fibre axons. The altered expression in CA3 neurons after ischaemia indicates that PAR4 may be involved in post-ischaemic adaptive mechanisms.

摘要

最近已经证明,蛋白酶激活受体 4(PAR4)在海马体中有明显的表达。在本研究中,作者定义了 PAR4 相关的亚细胞结构以及全脑缺血对 PAR4 表达的影响。为此,作者对未缺血和缺血后的大鼠组织进行了荧光免疫组织化学双重标记。在未缺血的动物中 - 除了在颗粒细胞和锥体细胞中的表达外 - 在 CA4 区还有密集的层状 PAR4 表达。进一步的分析表明,PAR4 仅在 CA4 区的苔藓纤维轴突上定位,这可以通过与 calbindin D-28k 的双重标记来检测,但与神经元胞体、中间神经元以及突触后、突触前和树突结构的标志物没有重叠。缺血后 3 天和 14 天,CA1 神经元发生变性,因此在 CA1 带中没有 PAR4 信号。在大多数其他海马结构中,PAR4 的表达没有变化,除了 CA3 区。在此,纤维相关的 PAR4 信号在缺血后减少并解体。此外,在缺血后 14 天,CA3 区还显示出 PAR4 从膜结合的神经元定位到弥散的细胞体定位的重新分布。综上所述,本研究首次证明 PAR4 定位于苔藓纤维轴突。缺血后 CA3 神经元表达的改变表明,PAR4 可能参与了缺血后的适应机制。

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